[ { "gene_id": 11287, "description": "PZP alpha-2-macroglobulin like 2", "gene_symbol": "[\"Pzp2\"]", "do": null }, { "gene_id": 11303, "description": "ATP-binding cassette, sub-family A member 1", "gene_symbol": "[\"Abca1\"]", "do": "[{\"label\":\"Tangier disease\",\"id\":\"DOID:1388\"}]" }, { "gene_id": 11304, "description": "ATP-binding cassette, sub-family A member 4", "gene_symbol": "[\"Abca4\"]", "do": "[{\"label\":\"Stargardt disease\",\"id\":\"DOID:0050817\"},{\"label\":\"cone-rod dystrophy 3\",\"id\":\"DOID:0111013\"},{\"label\":\"retinitis pigmentosa 19\",\"id\":\"DOID:0110354\"}]" }, { "gene_id": 11305, "description": "ATP-binding cassette, sub-family A member 2", "gene_symbol": "[\"Abca2\"]", "do": null }, { "gene_id": 11308, "description": "abl interactor 1", "gene_symbol": "[\"Abi1\"]", "do": null }, { "gene_id": 11350, "description": "Abl proto-oncogene 1, non-receptor tyrosine kinase", "gene_symbol": "[\"Abl1\"]", "do": null }, { "gene_id": 11364, "description": "acyl-Coenzyme A dehydrogenase, medium chain", "gene_symbol": "[\"Acadm\"]", "do": "[{\"label\":\"medium chain acyl-CoA dehydrogenase deficiency\",\"id\":\"DOID:0080153\"}]" }, { "gene_id": 11370, "description": "acyl-Coenzyme A dehydrogenase, very long chain", "gene_symbol": "[\"Acadvl\"]", "do": "[{\"label\":\"very long chain acyl-CoA dehydrogenase deficiency\",\"id\":\"DOID:0080155\"}]" }, { "gene_id": 11409, "description": "acyl-Coenzyme A dehydrogenase, short chain", "gene_symbol": "[\"Acads\"]", "do": "[{\"label\":\"short chain acyl-CoA dehydrogenase deficiency\",\"id\":\"DOID:0080154\"}]" }, { "gene_id": 11416, "description": "solute carrier family 33 (acetyl-CoA transporter), member 1", "gene_symbol": "[\"Slc33a1\"]", "do": null }, { "gene_id": 11418, "description": "acid-sensing ion channel 2", "gene_symbol": "[\"Asic2\"]", "do": null }, { "gene_id": 11419, "description": "acid-sensing ion channel 1", "gene_symbol": "[\"Asic1\"]", "do": null }, { "gene_id": 11421, "description": "angiotensin I converting enzyme", "gene_symbol": "[\"Ace\"]", "do": null }, { "gene_id": 11423, "description": "acetylcholinesterase", "gene_symbol": "[\"Ache\"]", "do": null }, { "gene_id": 11425, "description": "apolipoprotein C-IV", "gene_symbol": "[\"Apoc4\"]", "do": null }, { "gene_id": 11432, "description": "acid phosphatase 2, lysosomal", "gene_symbol": "[\"Acp2\"]", "do": null }, { "gene_id": 11433, "description": "acid phosphatase 5, tartrate resistant", "gene_symbol": "[\"Acp5\"]", "do": null }, { "gene_id": 11434, "description": "acrosin prepropeptide", "gene_symbol": "[\"Acr\"]", "do": null }, { "gene_id": 11435, "description": "cholinergic receptor nicotinic alpha 1 subunit", "gene_symbol": "[\"Chrna1\"]", "do": null }, { "gene_id": 11438, "description": "cholinergic receptor, nicotinic, alpha polypeptide 4", "gene_symbol": "[\"Chrna4\"]", "do": null }, { "gene_id": 11440, "description": "cholinergic receptor, nicotinic, alpha polypeptide 6", "gene_symbol": "[\"Chrna6\"]", "do": null }, { "gene_id": 11441, "description": "cholinergic receptor, nicotinic, alpha polypeptide 7", "gene_symbol": "[\"Chrna7\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 11443, "description": "cholinergic receptor nicotinic beta 1 subunit", "gene_symbol": "[\"Chrnb1\"]", "do": null }, { "gene_id": 11444, "description": "cholinergic receptor nicotinic beta 2 subunit", "gene_symbol": "[\"Chrnb2\"]", "do": "[{\"label\":\"attention deficit hyperactivity disorder\",\"id\":\"DOID:1094\"},{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"autosomal dominant nocturnal frontal lobe epilepsy 3\",\"id\":\"DOID:0060684\"}]" }, { "gene_id": 11447, "description": "cholinergic receptor, nicotinic, delta polypeptide", "gene_symbol": "[\"Chrnd\"]", "do": "[{\"label\":\"congenital myasthenic syndrome 3A\",\"id\":\"DOID:0110666\"}]" }, { "gene_id": 11448, "description": "cholinergic receptor, nicotinic, epsilon polypeptide", "gene_symbol": "[\"Chrne\"]", "do": "[{\"label\":\"congenital myasthenic syndrome 4A\",\"id\":\"DOID:0110678\"},{\"label\":\"congenital myasthenic syndrome 4C\",\"id\":\"DOID:0110679\"}]" }, { "gene_id": 11450, "description": "adiponectin, C1Q and collagen domain containing", "gene_symbol": "[\"Adipoq\"]", "do": null }, { "gene_id": 11459, "description": "actin alpha 1, skeletal muscle", "gene_symbol": "[\"Acta1\"]", "do": "[{\"label\":\"nemaline myopathy 3\",\"id\":\"DOID:0110927\"}]" }, { "gene_id": 11461, "description": "actin, beta", "gene_symbol": "[\"Actb\"]", "do": null }, { "gene_id": 11464, "description": "actin, alpha, cardiac muscle 1", "gene_symbol": "[\"Actc1\"]", "do": "[{\"label\":\"dilated cardiomyopathy 1R\",\"id\":\"DOID:0110456\"}]" }, { "gene_id": 11465, "description": "actin, gamma, cytoplasmic 1", "gene_symbol": "[\"Actg1\"]", "do": null }, { "gene_id": 11470, "description": "actin-like 7a", "gene_symbol": "[\"Actl7a\"]", "do": null }, { "gene_id": 11472, "description": "actinin alpha 2", "gene_symbol": "[\"Actn2\"]", "do": null }, { "gene_id": 11474, "description": "actinin alpha 3", "gene_symbol": "[\"Actn3\"]", "do": null }, { "gene_id": 11475, "description": "actin alpha 2, smooth muscle, aorta", "gene_symbol": "[\"Acta2\"]", "do": null }, { "gene_id": 11477, "description": "activin A receptor, type 1", "gene_symbol": "[\"Acvr1\"]", "do": "[{\"label\":\"fibrodysplasia ossificans progressiva\",\"id\":\"DOID:13374\"}]" }, { "gene_id": 11479, "description": "activin A receptor, type 1B", "gene_symbol": "[\"Acvr1b\"]", "do": null }, { "gene_id": 11480, "description": "activin receptor IIA", "gene_symbol": "[\"Acvr2a\"]", "do": "[{\"label\":\"Weissenbacher-Zweymuller syndrome\",\"id\":\"DOID:4258\"}]" }, { "gene_id": 11481, "description": "activin receptor IIB", "gene_symbol": "[\"Acvr2b\"]", "do": "[{\"label\":\"right atrial isomerism\",\"id\":\"DOID:0060856\"},{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 11482, "description": "activin A receptor, type II-like 1", "gene_symbol": "[\"Acvrl1\"]", "do": "[{\"label\":\"arteriovenous malformations of the brain\",\"id\":\"DOID:0060688\"},{\"label\":\"hereditary hemorrhagic telangiectasia\",\"id\":\"DOID:1270\"}]" }, { "gene_id": 11487, "description": "a disintegrin and metallopeptidase domain 10", "gene_symbol": "[\"Adam10\"]", "do": null }, { "gene_id": 11488, "description": "a disintegrin and metallopeptidase domain 11", "gene_symbol": "[\"Adam11\"]", "do": null }, { "gene_id": 11489, "description": "ADAM metallopeptidase domain 12", "gene_symbol": "[\"Adam12\"]", "do": null }, { "gene_id": 11490, "description": "ADAM metallopeptidase domain 15", "gene_symbol": "[\"Adam15\"]", "do": null }, { "gene_id": 11491, "description": "a disintegrin and metallopeptidase domain 17", "gene_symbol": "[\"Adam17\"]", "do": "[{\"label\":\"atopic dermatitis\",\"id\":\"DOID:3310\"}]" }, { "gene_id": 11492, "description": "ADAM metallopeptidase domain 19", "gene_symbol": "[\"Adam19\"]", "do": null }, { "gene_id": 11495, "description": "a disintegrin and metallopeptidase domain 2", "gene_symbol": "[\"Adam2\"]", "do": null }, { "gene_id": 11496, "description": "a disintegrin and metallopeptidase domain 22", "gene_symbol": "[\"Adam22\"]", "do": null }, { "gene_id": 11497, "description": "ADAM metallopeptidase domain 3", "gene_symbol": "[\"Adam3\"]", "do": null }, { "gene_id": 11498, "description": "a disintegrin and metallopeptidase domain 4", "gene_symbol": "[\"Adam4\"]", "do": null }, { "gene_id": 11499, "description": "a disintegrin and metallopeptidase domain 5", "gene_symbol": "[\"Adam5\"]", "do": null }, { "gene_id": 11500, "description": "a disintegrin and metallopeptidase domain 7", "gene_symbol": "[\"Adam7\"]", "do": null }, { "gene_id": 11501, "description": "a disintegrin and metallopeptidase domain 8", "gene_symbol": "[\"Adam8\"]", "do": null }, { "gene_id": 11502, "description": "ADAM metallopeptidase domain 9", "gene_symbol": "[\"Adam9\"]", "do": "[{\"label\":\"cone-rod dystrophy 9\",\"id\":\"DOID:0111020\"}]" }, { "gene_id": 11504, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 1", "gene_symbol": "[\"Adamts1\"]", "do": "[{\"label\":\"urinary tract obstruction\",\"id\":\"DOID:5200\"}]" }, { "gene_id": 11513, "description": "adenylate cyclase 7", "gene_symbol": "[\"Adcy7\"]", "do": null }, { "gene_id": 11514, "description": "adenylate cyclase 8", "gene_symbol": "[\"Adcy8\"]", "do": null }, { "gene_id": 11515, "description": "adenylate cyclase 9", "gene_symbol": "[\"Adcy9\"]", "do": null }, { "gene_id": 11517, "description": "adenylate cyclase activating polypeptide 1 receptor 1", "gene_symbol": "[\"Adcyap1r1\"]", "do": null }, { "gene_id": 11518, "description": "adducin 1", "gene_symbol": "[\"Add1\"]", "do": "[{\"label\":\"hydrocephalus\",\"id\":\"DOID:10908\"}]" }, { "gene_id": 11519, "description": "adducin 2", "gene_symbol": "[\"Add2\"]", "do": null }, { "gene_id": 11520, "description": "perilipin 2", "gene_symbol": "[\"Plin2\"]", "do": null }, { "gene_id": 11522, "description": "alcohol dehydrogenase 1 (class I)", "gene_symbol": "[\"Adh1\"]", "do": null }, { "gene_id": 11529, "description": "alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide", "gene_symbol": "[\"Adh7\"]", "do": "[{\"label\":\"Parkinson's disease\",\"id\":\"DOID:14330\"}]" }, { "gene_id": 11536, "description": "G protein-coupled receptor 182", "gene_symbol": "[\"Gpr182\"]", "do": null }, { "gene_id": 11537, "description": "complement factor D", "gene_symbol": "[\"Cfd\"]", "do": null }, { "gene_id": 11538, "description": "activity-dependent neuroprotective protein", "gene_symbol": "[\"Adnp\"]", "do": null }, { "gene_id": 11539, "description": "adenosine A1 receptor", "gene_symbol": "[\"Adora1\"]", "do": null }, { "gene_id": 11540, "description": "adenosine A2a receptor", "gene_symbol": "[\"Adora2a\"]", "do": "[{\"label\":\"myopia\",\"id\":\"DOID:11830\"},{\"label\":\"primary pulmonary hypertension\",\"id\":\"DOID:14557\"}]" }, { "gene_id": 11541, "description": "adenosine A2b receptor", "gene_symbol": "[\"Adora2b\"]", "do": null }, { "gene_id": 11544, "description": "ADP-ribosylarginine hydrolase", "gene_symbol": "[\"Adprh\"]", "do": null }, { "gene_id": 11546, "description": "poly (ADP-ribose) polymerase family, member 2", "gene_symbol": "[\"Parp2\"]", "do": null }, { "gene_id": 11548, "description": "adrenergic receptor, alpha 1b", "gene_symbol": "[\"Adra1b\"]", "do": null }, { "gene_id": 11549, "description": "adrenergic receptor, alpha 1a", "gene_symbol": "[\"Adra1a\"]", "do": null }, { "gene_id": 11551, "description": "adrenergic receptor, alpha 2a", "gene_symbol": "[\"Adra2a\"]", "do": null }, { "gene_id": 11553, "description": "adrenergic receptor, alpha 2c", "gene_symbol": "[\"Adra2c\"]", "do": null }, { "gene_id": 11554, "description": "adrenergic receptor, beta 1", "gene_symbol": "[\"Adrb1\"]", "do": null }, { "gene_id": 11555, "description": "adrenergic receptor, beta 2", "gene_symbol": "[\"Adrb2\"]", "do": null }, { "gene_id": 11556, "description": "adrenergic receptor, beta 3", "gene_symbol": "[\"Adrb3\"]", "do": null }, { "gene_id": 11568, "description": "AE binding protein 1", "gene_symbol": "[\"Aebp1\"]", "do": null }, { "gene_id": 11571, "description": "cysteine-rich secretory protein 1", "gene_symbol": "[\"Crisp1\"]", "do": null }, { "gene_id": 11572, "description": "cysteine-rich secretory protein 3", "gene_symbol": "[\"Crisp3\"]", "do": null }, { "gene_id": 11576, "description": "alpha fetoprotein", "gene_symbol": "[\"Afp\"]", "do": null }, { "gene_id": 11593, "description": "aspartylglucosaminidase", "gene_symbol": "[\"Aga\"]", "do": "[{\"label\":\"aspartylglucosaminuria\",\"id\":\"DOID:0050461\"}]" }, { "gene_id": 11595, "description": "aggrecan", "gene_symbol": "[\"Acan\"]", "do": "[{\"label\":\"achondroplasia\",\"id\":\"DOID:4480\"}]" }, { "gene_id": 11596, "description": "advanced glycosylation end product-specific receptor", "gene_symbol": "[\"Ager\"]", "do": null }, { "gene_id": 11600, "description": "angiopoietin 1", "gene_symbol": "[\"Angpt1\"]", "do": null }, { "gene_id": 11601, "description": "angiopoietin 2", "gene_symbol": "[\"Angpt2\"]", "do": null }, { "gene_id": 11602, "description": "angiopoietin 4", "gene_symbol": "[\"Angpt4\"]", "do": null }, { "gene_id": 11603, "description": "agrin", "gene_symbol": "[\"Agrn\"]", "do": "[{\"label\":\"congenital myasthenic syndrome 8\",\"id\":\"DOID:0110657\"}]" }, { "gene_id": 11605, "description": "galactosidase, alpha", "gene_symbol": "[\"Gla\"]", "do": "[{\"label\":\"Fabry disease\",\"id\":\"DOID:14499\"}]" }, { "gene_id": 11607, "description": "angiotensin II receptor, type 1a", "gene_symbol": "[\"Agtr1a\"]", "do": null }, { "gene_id": 11608, "description": "angiotensin II receptor, type 1b", "gene_symbol": "[\"Agtr1b\"]", "do": null }, { "gene_id": 11609, "description": "angiotensin II receptor, type 2", "gene_symbol": "[\"Agtr2\"]", "do": null }, { "gene_id": 11625, "description": "alpha-2-HS-glycoprotein", "gene_symbol": "[\"Ahsg\"]", "do": null }, { "gene_id": 11632, "description": "aryl-hydrocarbon receptor-interacting protein", "gene_symbol": "[\"Aip\"]", "do": null }, { "gene_id": 11636, "description": "adenylate kinase 1", "gene_symbol": "[\"Ak1\"]", "do": null }, { "gene_id": 11640, "description": "A kinase anchor protein 1", "gene_symbol": "[\"Akap1\"]", "do": null }, { "gene_id": 11647, "description": "alkaline phosphatase, liver/bone/kidney", "gene_symbol": "[\"Alpl\"]", "do": "[{\"label\":\"adult hypophosphatasia\",\"id\":\"DOID:0110913\"},{\"label\":\"childhood hypophosphatasia\",\"id\":\"DOID:0110915\"},{\"label\":\"infantile hypophosphatasia\",\"id\":\"DOID:0110914\"}]" }, { "gene_id": 11650, "description": "alkaline phosphatase, placental-like 2", "gene_symbol": "[\"Alppl2\"]", "do": null }, { "gene_id": 11651, "description": "Akt serine/threonine kinase 1", "gene_symbol": "[\"Akt1\"]", "do": "[{\"label\":\"Proteus syndrome\",\"id\":\"DOID:13482\"},{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 11652, "description": "Akt serine/threonine kinase 2", "gene_symbol": "[\"Akt2\"]", "do": "[{\"label\":\"polycystic ovary syndrome\",\"id\":\"DOID:11612\"},{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 11658, "description": "activated leukocyte cell adhesion molecule", "gene_symbol": "[\"Alcam\"]", "do": null }, { "gene_id": 11666, "description": "ATP-binding cassette, sub-family D member 1", "gene_symbol": "[\"Abcd1\"]", "do": "[{\"label\":\"adrenoleukodystrophy\",\"id\":\"DOID:10588\"}]" }, { "gene_id": 11668, "description": "aldehyde dehydrogenase family 1, subfamily A1", "gene_symbol": "[\"Aldh1a1\"]", "do": null }, { "gene_id": 11669, "description": "aldehyde dehydrogenase 2, mitochondrial", "gene_symbol": "[\"Aldh2\"]", "do": null }, { "gene_id": 11674, "description": "aldolase A, fructose-bisphosphate", "gene_symbol": "[\"Aldoa\"]", "do": null }, { "gene_id": 11676, "description": "aldolase C, fructose-bisphosphate", "gene_symbol": "[\"Aldoc\"]", "do": null }, { "gene_id": 11677, "description": "aldo-keto reductase family 1 member B", "gene_symbol": "[\"Akr1b1\"]", "do": null }, { "gene_id": 11682, "description": "anaplastic lymphoma kinase", "gene_symbol": "[\"Alk\"]", "do": null }, { "gene_id": 11699, "description": "alpha 1 microglobulin/bikunin precursor", "gene_symbol": "[\"Ambp\"]", "do": null }, { "gene_id": 11705, "description": "anti-Mullerian hormone", "gene_symbol": "[\"Amh\"]", "do": null }, { "gene_id": 11722, "description": "amylase 1, salivary", "gene_symbol": "[\"Amy1\"]", "do": null }, { "gene_id": 11735, "description": "ankyrin 3, epithelial", "gene_symbol": "[\"Ank3\"]", "do": null }, { "gene_id": 11737, "description": "acidic nuclear phosphoprotein 32 family member A", "gene_symbol": "[\"Anp32a\"]", "do": null }, { "gene_id": 11739, "description": "solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4", "gene_symbol": "[\"Slc25a4\"]", "do": null }, { "gene_id": 11740, "description": "solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 5", "gene_symbol": "[\"Slc25a5\"]", "do": null }, { "gene_id": 11746, "description": "annexin A4", "gene_symbol": "[\"Anxa4\"]", "do": null }, { "gene_id": 11747, "description": "annexin A5", "gene_symbol": "[\"Anxa5\"]", "do": null }, { "gene_id": 11749, "description": "annexin A6", "gene_symbol": "[\"Anxa6\"]", "do": null }, { "gene_id": 11750, "description": "annexin A7", "gene_symbol": "[\"Anxa7\"]", "do": null }, { "gene_id": 11754, "description": "amine oxidase, copper containing 3", "gene_symbol": "[\"Aoc3\"]", "do": null }, { "gene_id": 11757, "description": "peroxiredoxin 3", "gene_symbol": "[\"Prdx3\"]", "do": null }, { "gene_id": 11758, "description": "peroxiredoxin 6", "gene_symbol": "[\"Prdx6\"]", "do": null }, { "gene_id": 11765, "description": "adaptor protein complex AP-1, gamma 1 subunit", "gene_symbol": "[\"Ap1g1\"]", "do": null }, { "gene_id": 11771, "description": "adaptor-related protein complex 2, alpha 1 subunit", "gene_symbol": "[\"Ap2a1\"]", "do": null }, { "gene_id": 11772, "description": "adaptor-related protein complex 2, alpha 2 subunit", "gene_symbol": "[\"Ap2a2\"]", "do": null }, { "gene_id": 11773, "description": "adaptor-related protein complex 2, mu 1 subunit", "gene_symbol": "[\"Ap2m1\"]", "do": null }, { "gene_id": 11774, "description": "adaptor-related protein complex 3, beta 1 subunit", "gene_symbol": "[\"Ap3b1\"]", "do": "[{\"label\":\"Hermansky-Pudlak syndrome 2\",\"id\":\"DOID:0060540\"},{\"label\":\"platelet storage pool deficiency\",\"id\":\"DOID:2223\"}]" }, { "gene_id": 11775, "description": "adaptor-related protein complex 3, beta 2 subunit", "gene_symbol": "[\"Ap3b2\"]", "do": null }, { "gene_id": 11785, "description": "amyloid beta precursor protein binding family B member 1", "gene_symbol": "[\"Apbb1\"]", "do": null }, { "gene_id": 11790, "description": "SPEG complex locus", "gene_symbol": "[\"Speg\"]", "do": null }, { "gene_id": 11800, "description": "apoptosis inhibitor 5", "gene_symbol": "[\"Api5\"]", "do": null }, { "gene_id": 11801, "description": "CD5 antigen-like", "gene_symbol": "[\"Cd5l\"]", "do": null }, { "gene_id": 11803, "description": "amyloid beta precursor like protein 1", "gene_symbol": "[\"Aplp1\"]", "do": null }, { "gene_id": 11804, "description": "amyloid beta precursor-like protein 2", "gene_symbol": "[\"Aplp2\"]", "do": null }, { "gene_id": 11814, "description": "apolipoprotein C-III", "gene_symbol": "[\"Apoc3\"]", "do": null }, { "gene_id": 11815, "description": "apolipoprotein D", "gene_symbol": "[\"Apod\"]", "do": null }, { "gene_id": 11818, "description": "apolipoprotein H", "gene_symbol": "[\"Apoh\"]", "do": null }, { "gene_id": 11819, "description": "nuclear receptor subfamily 2, group F, member 2", "gene_symbol": "[\"Nr2f2\"]", "do": "[{\"label\":\"congenital diaphragmatic hernia\",\"id\":\"DOID:3827\"},{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 11820, "description": "amyloid beta precursor protein", "gene_symbol": "[\"App\"]", "do": "[{\"label\":\"Alzheimer's disease\",\"id\":\"DOID:10652\"}]" }, { "gene_id": 11821, "description": "adenine phosphoribosyl transferase", "gene_symbol": "[\"Aprt\"]", "do": "[{\"label\":\"adenine phosphoribosyltransferase deficiency\",\"id\":\"DOID:0060350\"}]" }, { "gene_id": 11826, "description": "aquaporin 1", "gene_symbol": "[\"Aqp1\"]", "do": null }, { "gene_id": 11827, "description": "aquaporin 2", "gene_symbol": "[\"Aqp2\"]", "do": "[{\"label\":\"nephrogenic diabetes insipidus\",\"id\":\"DOID:12387\"}]" }, { "gene_id": 11828, "description": "aquaporin 3", "gene_symbol": "[\"Aqp3\"]", "do": "[{\"label\":\"nephrogenic diabetes insipidus\",\"id\":\"DOID:12387\"}]" }, { "gene_id": 11829, "description": "aquaporin 4", "gene_symbol": "[\"Aqp4\"]", "do": "[{\"label\":\"malaria\",\"id\":\"DOID:12365\"}]" }, { "gene_id": 11830, "description": "aquaporin 5", "gene_symbol": "[\"Aqp5\"]", "do": "[{\"label\":\"dry eye syndrome\",\"id\":\"DOID:10140\"}]" }, { "gene_id": 11831, "description": "aquaporin 6", "gene_symbol": "[\"Aqp6\"]", "do": null }, { "gene_id": 11833, "description": "aquaporin 8", "gene_symbol": "[\"Aqp8\"]", "do": null }, { "gene_id": 11836, "description": "Araf proto-oncogene, serine/threonine kinase", "gene_symbol": "[\"Araf\"]", "do": null }, { "gene_id": 11838, "description": "activity regulated cytoskeletal-associated protein", "gene_symbol": "[\"Arc\"]", "do": null }, { "gene_id": 11839, "description": "amphiregulin", "gene_symbol": "[\"Areg\"]", "do": null }, { "gene_id": 11843, "description": "ARF GTPase 4", "gene_symbol": "[\"Arf4\"]", "do": null }, { "gene_id": 11863, "description": "aryl hydrocarbon receptor nuclear translocator", "gene_symbol": "[\"Arnt\"]", "do": null }, { "gene_id": 11867, "description": "actin related protein 2/3 complex, subunit 1B", "gene_symbol": "[\"Arpc1b\"]", "do": null }, { "gene_id": 11870, "description": "ADP-ribosyltransferase 1", "gene_symbol": "[\"Art1\"]", "do": null }, { "gene_id": 11871, "description": "ADP-ribosyltransferase 2a", "gene_symbol": "[\"Art2a\"]", "do": null }, { "gene_id": 11872, "description": "ADP-ribosyltransferase 2b", "gene_symbol": "[\"Art2b\"]", "do": null }, { "gene_id": 11875, "description": "ADP-ribosyltransferase 5", "gene_symbol": "[\"Art5\"]", "do": null }, { "gene_id": 11876, "description": "artemin", "gene_symbol": "[\"Artn\"]", "do": null }, { "gene_id": 11881, "description": "arylsulfatase B", "gene_symbol": "[\"Arsb\"]", "do": "[{\"label\":\"mucopolysaccharidosis VI\",\"id\":\"DOID:12800\"}]" }, { "gene_id": 11883, "description": "arylsulfatase A", "gene_symbol": "[\"Arsa\"]", "do": "[{\"label\":\"metachromatic leukodystrophy\",\"id\":\"DOID:10581\"}]" }, { "gene_id": 11886, "description": "N-acylsphingosine amidohydrolase 1", "gene_symbol": "[\"Asah1\"]", "do": "[{\"label\":\"Farber lipogranulomatosis\",\"id\":\"DOID:0050464\"}]" }, { "gene_id": 11889, "description": "asialoglycoprotein receptor 1", "gene_symbol": "[\"Asgr1\"]", "do": null }, { "gene_id": 11890, "description": "asialoglycoprotein receptor 2", "gene_symbol": "[\"Asgr2\"]", "do": null }, { "gene_id": 11898, "description": "argininosuccinate synthetase 1", "gene_symbol": "[\"Ass1\"]", "do": "[{\"label\":\"citrullinemia\",\"id\":\"DOID:9273\"}]" }, { "gene_id": 11899, "description": "astrotactin 1", "gene_symbol": "[\"Astn1\"]", "do": null }, { "gene_id": 11905, "description": "serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1", "gene_symbol": "[\"Serpinc1\"]", "do": "[{\"label\":\"antithrombin III deficiency\",\"id\":\"DOID:3755\"}]" }, { "gene_id": 11908, "description": "activating transcription factor 1", "gene_symbol": "[\"Atf1\"]", "do": null }, { "gene_id": 11909, "description": "activating transcription factor 2", "gene_symbol": "[\"Atf2\"]", "do": "[{\"label\":\"meconium aspiration syndrome\",\"id\":\"DOID:11049\"},{\"label\":\"osteochondrodysplasia\",\"id\":\"DOID:2256\"}]" }, { "gene_id": 11910, "description": "activating transcription factor 3", "gene_symbol": "[\"Atf3\"]", "do": null }, { "gene_id": 11911, "description": "activating transcription factor 4", "gene_symbol": "[\"Atf4\"]", "do": null }, { "gene_id": 11928, "description": "ATPase, Na+/K+ transporting, alpha 1 polypeptide", "gene_symbol": "[\"Atp1a1\"]", "do": null }, { "gene_id": 11931, "description": "ATPase, Na+/K+ transporting, beta 1 polypeptide", "gene_symbol": "[\"Atp1b1\"]", "do": null }, { "gene_id": 11932, "description": "ATPase, Na+/K+ transporting, beta 2 polypeptide", "gene_symbol": "[\"Atp1b2\"]", "do": null }, { "gene_id": 11933, "description": "ATPase, Na+/K+ transporting, beta 3 polypeptide", "gene_symbol": "[\"Atp1b3\"]", "do": null }, { "gene_id": 11937, "description": "ATPase, Ca++ transporting, cardiac muscle, fast twitch 1", "gene_symbol": "[\"Atp2a1\"]", "do": null }, { "gene_id": 11938, "description": "ATPase, Ca++ transporting, cardiac muscle, slow twitch 2", "gene_symbol": "[\"Atp2a2\"]", "do": "[{\"label\":\"keratosis follicularis\",\"id\":\"DOID:2734\"}]" }, { "gene_id": 11941, "description": "ATPase, Ca++ transporting, plasma membrane 2", "gene_symbol": "[\"Atp2b2\"]", "do": null }, { "gene_id": 11944, "description": "ATPase, H+/K+ exchanging, gastric, alpha polypeptide", "gene_symbol": "[\"Atp4a\"]", "do": null }, { "gene_id": 11945, "description": "ATPase, H+/K+ exchanging, beta polypeptide", "gene_symbol": "[\"Atp4b\"]", "do": null }, { "gene_id": 11946, "description": "ATP synthase F1 subunit alpha", "gene_symbol": "[\"Atp5f1a\"]", "do": null }, { "gene_id": 11947, "description": "ATP synthase F1 subunit beta", "gene_symbol": "[\"Atp5f1b\"]", "do": null }, { "gene_id": 11949, "description": "ATP synthase F1 subunit gamma", "gene_symbol": "[\"Atp5f1c\"]", "do": null }, { "gene_id": 11957, "description": "ATP synthase peripheral stalk subunit F6", "gene_symbol": "[\"Atp5pf\"]", "do": null }, { "gene_id": 11964, "description": "ATPase, H+ transporting, lysosomal V1 subunit A", "gene_symbol": "[\"Atp6v1a\"]", "do": null }, { "gene_id": 11966, "description": "ATPase, H+ transporting, lysosomal V1 subunit B2", "gene_symbol": "[\"Atp6v1b2\"]", "do": "[{\"label\":\"autosomal dominant congenital deafness with onychodystrophy\",\"id\":\"DOID:0080720\"},{\"label\":\"epilepsy\",\"id\":\"DOID:1826\"}]" }, { "gene_id": 11974, "description": "ATPase, H+ transporting, lysosomal V0 subunit E", "gene_symbol": "[\"Atp6v0e\"]", "do": null }, { "gene_id": 11975, "description": "ATPase, H+ transporting, lysosomal V0 subunit A1", "gene_symbol": "[\"Atp6v0a1\"]", "do": null }, { "gene_id": 11977, "description": "ATPase, copper transporting, alpha polypeptide", "gene_symbol": "[\"Atp7a\"]", "do": "[{\"label\":\"Menkes disease\",\"id\":\"DOID:1838\"},{\"label\":\"X-linked distal spinal muscular atrophy 3\",\"id\":\"DOID:0111196\"},{\"label\":\"aortic aneurysm\",\"id\":\"DOID:3627\"},{\"label\":\"osteoarthritis\",\"id\":\"DOID:8398\"}]" }, { "gene_id": 11980, "description": "ATPase phospholipid transporting 8A1", "gene_symbol": "[\"Atp8a1\"]", "do": null }, { "gene_id": 11982, "description": "ATPase, class V, type 10A", "gene_symbol": "[\"Atp10a\"]", "do": null }, { "gene_id": 11987, "description": "solute carrier family 7 (cationic amino acid transporter, y+ system), member 1", "gene_symbol": "[\"Slc7a1\"]", "do": null }, { "gene_id": 11988, "description": "solute carrier family 7 (cationic amino acid transporter, y+ system), member 2", "gene_symbol": "[\"Slc7a2\"]", "do": null }, { "gene_id": 11989, "description": "solute carrier family 7 (cationic amino acid transporter, y+ system), member 3", "gene_symbol": "[\"Slc7a3\"]", "do": null }, { "gene_id": 11990, "description": "attractin", "gene_symbol": "[\"Atrn\"]", "do": null }, { "gene_id": 11994, "description": "protocadherin 15", "gene_symbol": "[\"Pcdh15\"]", "do": "[{\"label\":\"Usher syndrome type 1F\",\"id\":\"DOID:0110832\"},{\"label\":\"autosomal recessive nonsyndromic deafness 23\",\"id\":\"DOID:0110481\"}]" }, { "gene_id": 11998, "description": "arginine vasopressin", "gene_symbol": "[\"Avp\"]", "do": "[{\"label\":\"neurohypophyseal diabetes insipidus\",\"id\":\"DOID:12388\"}]" }, { "gene_id": 12000, "description": "arginine vasopressin receptor 2", "gene_symbol": "[\"Avpr2\"]", "do": "[{\"label\":\"X-linked nephrogenic diabetes insipidus\",\"id\":\"DOID:0081060\"},{\"label\":\"nephrogenic diabetes insipidus\",\"id\":\"DOID:12387\"}]" }, { "gene_id": 12007, "description": "alpha-2-glycoprotein 1, zinc", "gene_symbol": "[\"Azgp1\"]", "do": null }, { "gene_id": 12009, "description": "centrosomal protein 131", "gene_symbol": "[\"Cep131\"]", "do": null }, { "gene_id": 12015, "description": "BCL2-associated agonist of cell death", "gene_symbol": "[\"Bad\"]", "do": null }, { "gene_id": 12021, "description": "BRCA1 associated RING domain 1", "gene_symbol": "[\"Bard1\"]", "do": "[{\"label\":\"breast cancer\",\"id\":\"DOID:1612\"}]" }, { "gene_id": 12028, "description": "BCL2-associated X protein", "gene_symbol": "[\"Bax\"]", "do": null }, { "gene_id": 12032, "description": "brevican", "gene_symbol": "[\"Bcan\"]", "do": null }, { "gene_id": 12034, "description": "prohibitin 2", "gene_symbol": "[\"Phb2\"]", "do": null }, { "gene_id": 12036, "description": "branched chain aminotransferase 2, mitochondrial", "gene_symbol": "[\"Bcat2\"]", "do": "[{\"label\":\"maple syrup urine disease\",\"id\":\"DOID:9269\"}]" }, { "gene_id": 12038, "description": "butyrylcholinesterase", "gene_symbol": "[\"Bche\"]", "do": null }, { "gene_id": 12041, "description": "branched chain ketoacid dehydrogenase kinase", "gene_symbol": "[\"Bckdk\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"branched-chain keto acid dehydrogenase kinase deficiency\",\"id\":\"DOID:0090126\"}]" }, { "gene_id": 12051, "description": "B cell leukemia/lymphoma 3", "gene_symbol": "[\"Bcl3\"]", "do": null }, { "gene_id": 12054, "description": "B cell CLL/lymphoma 7B", "gene_symbol": "[\"Bcl7b\"]", "do": null }, { "gene_id": 12057, "description": "opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)", "gene_symbol": "[\"Opn1sw\"]", "do": null }, { "gene_id": 12061, "description": "bradykinin receptor, beta 1", "gene_symbol": "[\"Bdkrb1\"]", "do": null }, { "gene_id": 12062, "description": "bradykinin receptor, beta 2", "gene_symbol": "[\"Bdkrb2\"]", "do": null }, { "gene_id": 12064, "description": "brain derived neurotrophic factor", "gene_symbol": "[\"Bdnf\"]", "do": null }, { "gene_id": 12091, "description": "galactosidase, beta 1", "gene_symbol": "[\"Glb1\"]", "do": "[{\"label\":\"GM1 gangliosidosis\",\"id\":\"DOID:3322\"}]" }, { "gene_id": 12111, "description": "biglycan", "gene_symbol": "[\"Bgn\"]", "do": null }, { "gene_id": 12145, "description": "C-X-C motif chemokine receptor 5", "gene_symbol": "[\"Cxcr5\"]", "do": null }, { "gene_id": 12153, "description": "bone morphogenetic protein 1", "gene_symbol": "[\"Bmp1\"]", "do": null }, { "gene_id": 12154, "description": "bone morphogenetic protein 10", "gene_symbol": "[\"Bmp10\"]", "do": "[{\"label\":\"tetralogy of Fallot\",\"id\":\"DOID:6419\"}]" }, { "gene_id": 12155, "description": "bone morphogenetic protein 15", "gene_symbol": "[\"Bmp15\"]", "do": null }, { "gene_id": 12156, "description": "bone morphogenetic protein 2", "gene_symbol": "[\"Bmp2\"]", "do": null }, { "gene_id": 12159, "description": "bone morphogenetic protein 4", "gene_symbol": "[\"Bmp4\"]", "do": "[{\"label\":\"Axenfeld-Rieger syndrome type 3\",\"id\":\"DOID:0110122\"},{\"label\":\"atrioventricular septal defect\",\"id\":\"DOID:0050651\"},{\"label\":\"cleft palate-lateral synechia syndrome\",\"id\":\"DOID:0080313\"},{\"label\":\"fibrodysplasia ossificans progressiva\",\"id\":\"DOID:13374\"},{\"label\":\"physical disorder\",\"id\":\"DOID:0080015\"},{\"label\":\"urinary system disease\",\"id\":\"DOID:18\"}]" }, { "gene_id": 12160, "description": "bone morphogenetic protein 5", "gene_symbol": "[\"Bmp5\"]", "do": "[{\"label\":\"Meier-Gorlin syndrome\",\"id\":\"DOID:0060306\"}]" }, { "gene_id": 12161, "description": "bone morphogenetic protein 6", "gene_symbol": "[\"Bmp6\"]", "do": null }, { "gene_id": 12162, "description": "bone morphogenetic protein 7", "gene_symbol": "[\"Bmp7\"]", "do": "[{\"label\":\"obstructive sleep apnea\",\"id\":\"DOID:0050848\"},{\"label\":\"osteoarthritis\",\"id\":\"DOID:8398\"}]" }, { "gene_id": 12163, "description": "bone morphogenetic protein 8a", "gene_symbol": "[\"Bmp8a\"]", "do": null }, { "gene_id": 12164, "description": "bone morphogenetic protein 8b", "gene_symbol": "[\"Bmp8b\"]", "do": null }, { "gene_id": 12165, "description": "growth differentiation factor 2", "gene_symbol": "[\"Gdf2\"]", "do": null }, { "gene_id": 12166, "description": "bone morphogenetic protein receptor, type 1A", "gene_symbol": "[\"Bmpr1a\"]", "do": "[{\"label\":\"Ebstein anomaly\",\"id\":\"DOID:14289\"},{\"label\":\"Wolff-Parkinson-White syndrome\",\"id\":\"DOID:384\"},{\"label\":\"chromosome 10q23 deletion syndrome\",\"id\":\"DOID:0060389\"},{\"label\":\"juvenile polyposis syndrome\",\"id\":\"DOID:0050787\"},{\"label\":\"osteoarthritis\",\"id\":\"DOID:8398\"}]" }, { "gene_id": 12168, "description": "bone morphogenetic protein receptor type 2", "gene_symbol": "[\"Bmpr2\"]", "do": "[{\"label\":\"primary pulmonary hypertension\",\"id\":\"DOID:14557\"}]" }, { "gene_id": 12176, "description": "BCL2/adenovirus E1B interacting protein 3", "gene_symbol": "[\"Bnip3\"]", "do": null }, { "gene_id": 12181, "description": "block of proliferation 1", "gene_symbol": "[\"Bop1\"]", "do": null }, { "gene_id": 12182, "description": "bone marrow stromal cell antigen 1", "gene_symbol": "[\"Bst1\"]", "do": null }, { "gene_id": 12183, "description": "2,3-bisphosphoglycerate mutase", "gene_symbol": "[\"Bpgm\"]", "do": null }, { "gene_id": 12193, "description": "zinc finger protein 36, C3H type-like 2", "gene_symbol": "[\"Zfp36l2\"]", "do": null }, { "gene_id": 12209, "description": "bombesin-like receptor 3", "gene_symbol": "[\"Brs3\"]", "do": null }, { "gene_id": 12211, "description": "baculoviral IAP repeat-containing 6", "gene_symbol": "[\"Birc6\"]", "do": null }, { "gene_id": 12215, "description": "basigin", "gene_symbol": "[\"Bsg\"]", "do": null }, { "gene_id": 12217, "description": "bassoon", "gene_symbol": "[\"Bsn\"]", "do": "[{\"label\":\"epilepsy\",\"id\":\"DOID:1826\"}]" }, { "gene_id": 12223, "description": "betacellulin, epidermal growth factor family member", "gene_symbol": "[\"Btc\"]", "do": null }, { "gene_id": 12224, "description": "Kruppel-like transcription factor 5", "gene_symbol": "[\"Klf5\"]", "do": null }, { "gene_id": 12229, "description": "Bruton agammaglobulinemia tyrosine kinase", "gene_symbol": "[\"Btk\"]", "do": "[{\"label\":\"X-linked agammaglobulinemia\",\"id\":\"DOID:14179\"}]" }, { "gene_id": 12231, "description": "butyrophilin, subfamily 1, member A1", "gene_symbol": "[\"Btn1a1\"]", "do": null }, { "gene_id": 12235, "description": "BUB1, mitotic checkpoint serine/threonine kinase", "gene_symbol": "[\"Bub1\"]", "do": null }, { "gene_id": 12237, "description": "BUB3 mitotic checkpoint protein", "gene_symbol": "[\"Bub3\"]", "do": null }, { "gene_id": 12258, "description": "serine (or cysteine) peptidase inhibitor, clade G, member 1", "gene_symbol": "[\"Serping1\"]", "do": null }, { "gene_id": 12259, "description": "complement component 1, q subcomponent, alpha polypeptide", "gene_symbol": "[\"C1qa\"]", "do": "[{\"label\":\"epilepsy\",\"id\":\"DOID:1826\"},{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 12260, "description": "complement component 1, q subcomponent, beta polypeptide", "gene_symbol": "[\"C1qb\"]", "do": null }, { "gene_id": 12262, "description": "complement component 1, q subcomponent, C chain", "gene_symbol": "[\"C1qc\"]", "do": null }, { "gene_id": 12263, "description": "complement C2", "gene_symbol": "[\"C2\"]", "do": null }, { "gene_id": 12266, "description": "complement component 3", "gene_symbol": "[\"C3\"]", "do": "[{\"label\":\"complement component 3 deficiency\",\"id\":\"DOID:8354\"}]" }, { "gene_id": 12267, "description": "complement component 3a receptor 1", "gene_symbol": "[\"C3ar1\"]", "do": null }, { "gene_id": 12268, "description": "complement C4B (Chido blood group)", "gene_symbol": "[\"C4b\"]", "do": "[{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 12269, "description": "complement component 4 binding protein", "gene_symbol": "[\"C4bp\"]", "do": null }, { "gene_id": 12273, "description": "complement component 5a receptor 1", "gene_symbol": "[\"C5ar1\"]", "do": null }, { "gene_id": 12274, "description": "complement component 6", "gene_symbol": "[\"C6\"]", "do": null }, { "gene_id": 12279, "description": "complement component 9", "gene_symbol": "[\"C9\"]", "do": null }, { "gene_id": 12282, "description": "hypoxia up-regulated 1", "gene_symbol": "[\"Hyou1\"]", "do": null }, { "gene_id": 12286, "description": "calcium channel, voltage-dependent, P/Q type, alpha 1A subunit", "gene_symbol": "[\"Cacna1a\"]", "do": "[{\"label\":\"Lambert-Eaton myasthenic syndrome\",\"id\":\"DOID:0050214\"},{\"label\":\"cerebellar ataxia\",\"id\":\"DOID:0050753\"},{\"label\":\"childhood electroclinical syndrome\",\"id\":\"DOID:0050704\"},{\"label\":\"episodic ataxia type 2\",\"id\":\"DOID:0050990\"},{\"label\":\"familial hemiplegic migraine\",\"id\":\"DOID:0060178\"},{\"label\":\"generalized dystonia\",\"id\":\"DOID:0050835\"},{\"label\":\"spinocerebellar ataxia 6\",\"id\":\"DOID:0050956\"}]" }, { "gene_id": 12287, "description": "calcium channel, voltage-dependent, N type, alpha 1B subunit", "gene_symbol": "[\"Cacna1b\"]", "do": null }, { "gene_id": 12288, "description": "calcium channel, voltage-dependent, L type, alpha 1C subunit", "gene_symbol": "[\"Cacna1c\"]", "do": "[{\"label\":\"Timothy syndrome\",\"id\":\"DOID:0060173\"}]" }, { "gene_id": 12289, "description": "calcium channel, voltage-dependent, L type, alpha 1D subunit", "gene_symbol": "[\"Cacna1d\"]", "do": null }, { "gene_id": 12291, "description": "calcium channel, voltage-dependent, T type, alpha 1G subunit", "gene_symbol": "[\"Cacna1g\"]", "do": "[{\"label\":\"cerebellar ataxia type 42\",\"id\":\"DOID:0111742\"}]" }, { "gene_id": 12292, "description": "calcium channel, voltage-dependent, L type, alpha 1S subunit", "gene_symbol": "[\"Cacna1s\"]", "do": "[{\"label\":\"hypokalemic periodic paralysis\",\"id\":\"DOID:14452\"}]" }, { "gene_id": 12293, "description": "calcium channel, voltage-dependent, alpha2/delta subunit 1", "gene_symbol": "[\"Cacna2d1\"]", "do": null }, { "gene_id": 12294, "description": "calcium channel, voltage-dependent, alpha2/delta subunit 3", "gene_symbol": "[\"Cacna2d3\"]", "do": null }, { "gene_id": 12295, "description": "calcium channel, voltage-dependent, beta 1 subunit", "gene_symbol": "[\"Cacnb1\"]", "do": null }, { "gene_id": 12297, "description": "calcium channel, voltage-dependent, beta 3 subunit", "gene_symbol": "[\"Cacnb3\"]", "do": null }, { "gene_id": 12298, "description": "calcium channel, voltage-dependent, beta 4 subunit", "gene_symbol": "[\"Cacnb4\"]", "do": null }, { "gene_id": 12299, "description": "calcium channel, voltage-dependent, gamma subunit 1", "gene_symbol": "[\"Cacng1\"]", "do": null }, { "gene_id": 12300, "description": "calcium channel, voltage-dependent, gamma subunit 2", "gene_symbol": "[\"Cacng2\"]", "do": null }, { "gene_id": 12301, "description": "calcyclin binding protein", "gene_symbol": "[\"Cacybp\"]", "do": null }, { "gene_id": 12304, "description": "protein disulfide isomerase associated 4", "gene_symbol": "[\"Pdia4\"]", "do": null }, { "gene_id": 12305, "description": "discoidin domain receptor family, member 1", "gene_symbol": "[\"Ddr1\"]", "do": null }, { "gene_id": 12310, "description": "calcitonin/calcitonin-related polypeptide, alpha", "gene_symbol": "[\"Calca\"]", "do": null }, { "gene_id": 12311, "description": "calcitonin receptor", "gene_symbol": "[\"Calcr\"]", "do": null }, { "gene_id": 12317, "description": "calreticulin", "gene_symbol": "[\"Calr\"]", "do": "[{\"label\":\"congestive heart failure\",\"id\":\"DOID:6000\"}]" }, { "gene_id": 12321, "description": "calumenin", "gene_symbol": "[\"Calu\"]", "do": null }, { "gene_id": 12322, "description": "calcium/calmodulin-dependent protein kinase II alpha", "gene_symbol": "[\"Camk2a\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"bipolar disorder\",\"id\":\"DOID:3312\"}]" }, { "gene_id": 12323, "description": "calcium/calmodulin-dependent protein kinase II, beta", "gene_symbol": "[\"Camk2b\"]", "do": null }, { "gene_id": 12325, "description": "calcium/calmodulin-dependent protein kinase II gamma", "gene_symbol": "[\"Camk2g\"]", "do": null }, { "gene_id": 12330, "description": "calnexin", "gene_symbol": "[\"Canx\"]", "do": null }, { "gene_id": 12331, "description": "cyclase associated actin cytoskeleton regulatory protein 1", "gene_symbol": "[\"Cap1\"]", "do": null }, { "gene_id": 12348, "description": "carbonic anhydrase 11", "gene_symbol": "[\"Car11\"]", "do": null }, { "gene_id": 12351, "description": "carbonic anhydrase 4", "gene_symbol": "[\"Car4\"]", "do": null }, { "gene_id": 12352, "description": "carbonic anhydrase 5a, mitochondrial", "gene_symbol": "[\"Car5a\"]", "do": null }, { "gene_id": 12353, "description": "carbonic anhydrase 6", "gene_symbol": "[\"Car6\"]", "do": null }, { "gene_id": 12371, "description": "caspase 9", "gene_symbol": "[\"Casp9\"]", "do": null }, { "gene_id": 12372, "description": "calsequestrin 1", "gene_symbol": "[\"Casq1\"]", "do": null }, { "gene_id": 12373, "description": "calsequestrin 2", "gene_symbol": "[\"Casq2\"]", "do": "[{\"label\":\"catecholaminergic polymorphic ventricular tachycardia 2\",\"id\":\"DOID:0060676\"}]" }, { "gene_id": 12374, "description": "calcium-sensing receptor", "gene_symbol": "[\"Casr\"]", "do": "[{\"label\":\"autosomal dominant hypocalcemia 1\",\"id\":\"DOID:0090107\"},{\"label\":\"familial hypocalciuric hypercalcemia 1\",\"id\":\"DOID:0060700\"},{\"label\":\"hyperparathyroidism\",\"id\":\"DOID:13543\"}]" }, { "gene_id": 12380, "description": "calpastatin", "gene_symbol": "[\"Cast\"]", "do": null }, { "gene_id": 12386, "description": "catenin alpha 2", "gene_symbol": "[\"Ctnna2\"]", "do": null }, { "gene_id": 12387, "description": "catenin beta 1", "gene_symbol": "[\"Ctnnb1\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"exudative vitreoretinopathy\",\"id\":\"DOID:0050535\"},{\"label\":\"granulosa cell tumor\",\"id\":\"DOID:2999\"},{\"label\":\"ovarian cancer\",\"id\":\"DOID:2394\"},{\"label\":\"prostate cancer\",\"id\":\"DOID:10283\"},{\"label\":\"urinary bladder cancer\",\"id\":\"DOID:11054\"}]" }, { "gene_id": 12388, "description": "catenin delta 1", "gene_symbol": "[\"Ctnnd1\"]", "do": null }, { "gene_id": 12393, "description": "runt related transcription factor 2", "gene_symbol": "[\"Runx2\"]", "do": "[{\"label\":\"cleidocranial dysplasia\",\"id\":\"DOID:13994\"},{\"label\":\"congenital hypothyroidism\",\"id\":\"DOID:0050328\"}]" }, { "gene_id": 12401, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 6", "gene_symbol": "[\"Serpina6\"]", "do": "[{\"label\":\"corticosteroid-binding globulin deficiency\",\"id\":\"DOID:0090030\"}]" }, { "gene_id": 12402, "description": "Cbl proto-oncogene", "gene_symbol": "[\"Cbl\"]", "do": null }, { "gene_id": 12404, "description": "cerebellin 1 precursor protein", "gene_symbol": "[\"Cbln1\"]", "do": null }, { "gene_id": 12405, "description": "cerebellin 2 precursor protein", "gene_symbol": "[\"Cbln2\"]", "do": null }, { "gene_id": 12406, "description": "serine (or cysteine) peptidase inhibitor, clade H, member 1", "gene_symbol": "[\"Serpinh1\"]", "do": "[{\"label\":\"osteogenesis imperfecta type 10\",\"id\":\"DOID:0110346\"}]" }, { "gene_id": 12409, "description": "carbonyl reductase 2", "gene_symbol": "[\"Cbr2\"]", "do": null }, { "gene_id": 12416, "description": "chromobox 2", "gene_symbol": "[\"Cbx2\"]", "do": null }, { "gene_id": 12421, "description": "RB1-inducible coiled-coil 1", "gene_symbol": "[\"Rb1cc1\"]", "do": null }, { "gene_id": 12425, "description": "cholecystokinin A receptor", "gene_symbol": "[\"Cckar\"]", "do": null }, { "gene_id": 12426, "description": "cholecystokinin B receptor", "gene_symbol": "[\"Cckbr\"]", "do": null }, { "gene_id": 12457, "description": "nocturnin", "gene_symbol": "[\"Noct\"]", "do": null }, { "gene_id": 12458, "description": "C-C motif chemokine receptor 6", "gene_symbol": "[\"Ccr6\"]", "do": null }, { "gene_id": 12462, "description": "chaperonin containing TCP1 subunit 3", "gene_symbol": "[\"Cct3\"]", "do": null }, { "gene_id": 12469, "description": "chaperonin containing TCP1 subunit 8", "gene_symbol": "[\"Cct8\"]", "do": null }, { "gene_id": 12475, "description": "CD14 antigen", "gene_symbol": "[\"Cd14\"]", "do": null }, { "gene_id": 12476, "description": "CD151 antigen", "gene_symbol": "[\"Cd151\"]", "do": null }, { "gene_id": 12477, "description": "cytotoxic T-lymphocyte-associated protein 4", "gene_symbol": "[\"Ctla4\"]", "do": null }, { "gene_id": 12478, "description": "CD19 antigen", "gene_symbol": "[\"Cd19\"]", "do": null }, { "gene_id": 12479, "description": "CD1d1 antigen", "gene_symbol": "[\"Cd1d1\"]", "do": null }, { "gene_id": 12480, "description": "CD1d2 antigen", "gene_symbol": "[\"Cd1d2\"]", "do": null }, { "gene_id": 12481, "description": "CD2 antigen", "gene_symbol": "[\"Cd2\"]", "do": null }, { "gene_id": 12483, "description": "CD22 antigen", "gene_symbol": "[\"Cd22\"]", "do": null }, { "gene_id": 12484, "description": "CD24a antigen", "gene_symbol": "[\"Cd24a\"]", "do": null }, { "gene_id": 12487, "description": "CD28 antigen", "gene_symbol": "[\"Cd28\"]", "do": null }, { "gene_id": 12488, "description": "CD2-associated protein", "gene_symbol": "[\"Cd2ap\"]", "do": "[{\"label\":\"end stage renal disease\",\"id\":\"DOID:783\"},{\"label\":\"focal segmental glomerulosclerosis 3\",\"id\":\"DOID:0112245\"}]" }, { "gene_id": 12489, "description": "CD33 molecule", "gene_symbol": "[\"Cd33\"]", "do": null }, { "gene_id": 12490, "description": "CD34 antigen", "gene_symbol": "[\"Cd34\"]", "do": null }, { "gene_id": 12491, "description": "CD36 molecule", "gene_symbol": "[\"Cd36\"]", "do": "[{\"label\":\"platelet-type bleeding disorder 10\",\"id\":\"DOID:0111046\"}]" }, { "gene_id": 12492, "description": "scavenger receptor class B, member 2", "gene_symbol": "[\"Scarb2\"]", "do": "[{\"label\":\"progressive myoclonus epilepsy\",\"id\":\"DOID:891\"}]" }, { "gene_id": 12493, "description": "CD37 antigen", "gene_symbol": "[\"Cd37\"]", "do": null }, { "gene_id": 12494, "description": "CD38 antigen", "gene_symbol": "[\"Cd38\"]", "do": "[{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 12495, "description": "ectonucleoside triphosphate diphosphohydrolase 1", "gene_symbol": "[\"Entpd1\"]", "do": null }, { "gene_id": 12496, "description": "ectonucleoside triphosphate diphosphohydrolase 2", "gene_symbol": "[\"Entpd2\"]", "do": null }, { "gene_id": 12497, "description": "ectonucleoside triphosphate diphosphohydrolase 6", "gene_symbol": "[\"Entpd6\"]", "do": null }, { "gene_id": 12499, "description": "ectonucleoside triphosphate diphosphohydrolase 5", "gene_symbol": "[\"Entpd5\"]", "do": null }, { "gene_id": 12500, "description": "CD3 antigen, delta polypeptide", "gene_symbol": "[\"Cd3d\"]", "do": null }, { "gene_id": 12502, "description": "CD3 antigen, gamma polypeptide", "gene_symbol": "[\"Cd3g\"]", "do": null }, { "gene_id": 12504, "description": "CD4 antigen", "gene_symbol": "[\"Cd4\"]", "do": null }, { "gene_id": 12505, "description": "CD44 antigen", "gene_symbol": "[\"Cd44\"]", "do": null }, { "gene_id": 12506, "description": "CD48 antigen", "gene_symbol": "[\"Cd48\"]", "do": null }, { "gene_id": 12507, "description": "CD5 antigen", "gene_symbol": "[\"Cd5\"]", "do": null }, { "gene_id": 12508, "description": "CD53 antigen", "gene_symbol": "[\"Cd53\"]", "do": null }, { "gene_id": 12509, "description": "CD59a antigen", "gene_symbol": "[\"Cd59a\"]", "do": null }, { "gene_id": 12511, "description": "CD6 antigen", "gene_symbol": "[\"Cd6\"]", "do": null }, { "gene_id": 12512, "description": "CD63 antigen", "gene_symbol": "[\"Cd63\"]", "do": null }, { "gene_id": 12514, "description": "CD68 antigen", "gene_symbol": "[\"Cd68\"]", "do": null }, { "gene_id": 12515, "description": "CD69 antigen", "gene_symbol": "[\"Cd69\"]", "do": null }, { "gene_id": 12516, "description": "CD7 antigen", "gene_symbol": "[\"Cd7\"]", "do": null }, { "gene_id": 12517, "description": "CD72 antigen", "gene_symbol": "[\"Cd72\"]", "do": null }, { "gene_id": 12518, "description": "CD79A antigen (immunoglobulin-associated alpha)", "gene_symbol": "[\"Cd79a\"]", "do": null }, { "gene_id": 12519, "description": "CD80 antigen", "gene_symbol": "[\"Cd80\"]", "do": null }, { "gene_id": 12520, "description": "CD81 antigen", "gene_symbol": "[\"Cd81\"]", "do": null }, { "gene_id": 12521, "description": "CD82 antigen", "gene_symbol": "[\"Cd82\"]", "do": null }, { "gene_id": 12522, "description": "CD83 antigen", "gene_symbol": "[\"Cd83\"]", "do": null }, { "gene_id": 12523, "description": "CD84 antigen", "gene_symbol": "[\"Cd84\"]", "do": null }, { "gene_id": 12524, "description": "CD86 antigen", "gene_symbol": "[\"Cd86\"]", "do": "[{\"label\":\"Guillain-Barre syndrome\",\"id\":\"DOID:12842\"}]" }, { "gene_id": 12525, "description": "CD8 subunit alpha", "gene_symbol": "[\"Cd8a\"]", "do": null }, { "gene_id": 12526, "description": "CD8 subunit beta 1", "gene_symbol": "[\"Cd8b1\"]", "do": null }, { "gene_id": 12527, "description": "CD9 antigen", "gene_symbol": "[\"Cd9\"]", "do": null }, { "gene_id": 12530, "description": "cell division cycle 25A", "gene_symbol": "[\"Cdc25a\"]", "do": null }, { "gene_id": 12549, "description": "Rho GTPase activating protein 31", "gene_symbol": "[\"Arhgap31\"]", "do": null }, { "gene_id": 12550, "description": "cadherin 1", "gene_symbol": "[\"Cdh1\"]", "do": null }, { "gene_id": 12552, "description": "cadherin 11", "gene_symbol": "[\"Cdh11\"]", "do": null }, { "gene_id": 12554, "description": "cadherin 13", "gene_symbol": "[\"Cdh13\"]", "do": null }, { "gene_id": 12555, "description": "cadherin 15", "gene_symbol": "[\"Cdh15\"]", "do": null }, { "gene_id": 12556, "description": "cadherin 16", "gene_symbol": "[\"Cdh16\"]", "do": null }, { "gene_id": 12557, "description": "cadherin 17", "gene_symbol": "[\"Cdh17\"]", "do": null }, { "gene_id": 12558, "description": "cadherin 2", "gene_symbol": "[\"Cdh2\"]", "do": "[{\"label\":\"attention deficit hyperactivity disorder\",\"id\":\"DOID:1094\"}]" }, { "gene_id": 12560, "description": "cadherin 3", "gene_symbol": "[\"Cdh3\"]", "do": null }, { "gene_id": 12561, "description": "cadherin 4", "gene_symbol": "[\"Cdh4\"]", "do": null }, { "gene_id": 12562, "description": "cadherin 5", "gene_symbol": "[\"Cdh5\"]", "do": "[{\"label\":\"exudative vitreoretinopathy\",\"id\":\"DOID:0050535\"}]" }, { "gene_id": 12563, "description": "cadherin 6", "gene_symbol": "[\"Cdh6\"]", "do": null }, { "gene_id": 12564, "description": "cadherin 8", "gene_symbol": "[\"Cdh8\"]", "do": null }, { "gene_id": 12608, "description": "CCAAT/enhancer binding protein beta", "gene_symbol": "[\"Cebpb\"]", "do": "[{\"label\":\"osteochondrodysplasia\",\"id\":\"DOID:2256\"},{\"label\":\"viral infectious disease\",\"id\":\"DOID:934\"}]" }, { "gene_id": 12613, "description": "carboxyl ester lipase", "gene_symbol": "[\"Cel\"]", "do": null }, { "gene_id": 12614, "description": "cadherin, EGF LAG seven-pass G-type receptor 1", "gene_symbol": "[\"Celsr1\"]", "do": null }, { "gene_id": 12622, "description": "cerberus 1, DAN family BMP antagonist", "gene_symbol": "[\"Cer1\"]", "do": null }, { "gene_id": 12623, "description": "carboxylesterase 1G", "gene_symbol": "[\"Ces1g\"]", "do": null }, { "gene_id": 12627, "description": "cryptic, EGF-CFC family member 1", "gene_symbol": "[\"Cfc1\"]", "do": "[{\"label\":\"dextro-looped transposition of the great arteries\",\"id\":\"DOID:0060770\"},{\"label\":\"double outlet right ventricle\",\"id\":\"DOID:6406\"},{\"label\":\"right atrial isomerism\",\"id\":\"DOID:0060856\"},{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 12628, "description": "complement component factor h", "gene_symbol": "[\"Cfh\"]", "do": "[{\"label\":\"age related macular degeneration 4\",\"id\":\"DOID:0110017\"},{\"label\":\"atypical hemolytic-uremic syndrome\",\"id\":\"DOID:0080301\"},{\"label\":\"hemolytic-uremic syndrome\",\"id\":\"DOID:12554\"},{\"label\":\"membranoproliferative glomerulonephritis\",\"id\":\"DOID:2920\"}]" }, { "gene_id": 12630, "description": "complement component factor i", "gene_symbol": "[\"Cfi\"]", "do": "[{\"label\":\"glomerulonephritis\",\"id\":\"DOID:2921\"}]" }, { "gene_id": 12631, "description": "cofilin 1, non-muscle", "gene_symbol": "[\"Cfl1\"]", "do": null }, { "gene_id": 12638, "description": "cystic fibrosis transmembrane conductance regulator", "gene_symbol": "[\"Cftr\"]", "do": "[{\"label\":\"cystic fibrosis\",\"id\":\"DOID:1485\"}]" }, { "gene_id": 12640, "description": "glycoprotein hormones, alpha subunit", "gene_symbol": "[\"Cga\"]", "do": null }, { "gene_id": 12642, "description": "cholesterol 25-hydroxylase", "gene_symbol": "[\"Ch25h\"]", "do": null }, { "gene_id": 12643, "description": "chondroadherin", "gene_symbol": "[\"Chad\"]", "do": null }, { "gene_id": 12652, "description": "chromogranin A", "gene_symbol": "[\"Chga\"]", "do": null }, { "gene_id": 12653, "description": "chromogranin B", "gene_symbol": "[\"Chgb\"]", "do": null }, { "gene_id": 12654, "description": "chitinase 3 like 1", "gene_symbol": "[\"Chi3l1\"]", "do": null }, { "gene_id": 12655, "description": "chitinase-like 3", "gene_symbol": "[\"Chil3\"]", "do": null }, { "gene_id": 12659, "description": "oviductal glycoprotein 1", "gene_symbol": "[\"Ovgp1\"]", "do": null }, { "gene_id": 12661, "description": "cell adhesion molecule L1-like", "gene_symbol": "[\"Chl1\"]", "do": null }, { "gene_id": 12667, "description": "chordin", "gene_symbol": "[\"Chrd\"]", "do": "[{\"label\":\"DiGeorge syndrome\",\"id\":\"DOID:11198\"},{\"label\":\"velocardiofacial syndrome\",\"id\":\"DOID:12583\"}]" }, { "gene_id": 12669, "description": "cholinergic receptor, muscarinic 1, CNS", "gene_symbol": "[\"Chrm1\"]", "do": null }, { "gene_id": 12671, "description": "cholinergic receptor, muscarinic 3, cardiac", "gene_symbol": "[\"Chrm3\"]", "do": "[{\"label\":\"megacystis-microcolon-intestinal hypoperistalsis syndrome\",\"id\":\"DOID:0060610\"}]" }, { "gene_id": 12672, "description": "cholinergic receptor, muscarinic 4", "gene_symbol": "[\"Chrm4\"]", "do": null }, { "gene_id": 12686, "description": "ELOVL fatty acid elongase 3", "gene_symbol": "[\"Elovl3\"]", "do": null }, { "gene_id": 12695, "description": "PATJ, crumbs cell polarity complex component", "gene_symbol": "[\"Patj\"]", "do": null }, { "gene_id": 12721, "description": "coronin, actin binding protein 1A", "gene_symbol": "[\"Coro1a\"]", "do": "[{\"label\":\"severe combined immunodeficiency 104\",\"id\":\"DOID:0090014\"}]" }, { "gene_id": 12722, "description": "chloride channel accessory 3A1", "gene_symbol": "[\"Clca3a1\"]", "do": null }, { "gene_id": 12724, "description": "chloride channel, voltage-sensitive 2", "gene_symbol": "[\"Clcn2\"]", "do": "[{\"label\":\"leukodystrophy\",\"id\":\"DOID:10579\"},{\"label\":\"primary hyperaldosteronism\",\"id\":\"DOID:446\"}]" }, { "gene_id": 12725, "description": "chloride channel, voltage-sensitive 3", "gene_symbol": "[\"Clcn3\"]", "do": "[{\"label\":\"neuronal ceroid lipofuscinosis 3\",\"id\":\"DOID:0110731\"}]" }, { "gene_id": 12728, "description": "chloride channel, voltage-sensitive 5", "gene_symbol": "[\"Clcn5\"]", "do": "[{\"label\":\"Dent disease\",\"id\":\"DOID:0050699\"}]" }, { "gene_id": 12733, "description": "chloride channel, voltage-sensitive Ka", "gene_symbol": "[\"Clcnka\"]", "do": "[{\"label\":\"nephrogenic diabetes insipidus\",\"id\":\"DOID:12387\"}]" }, { "gene_id": 12748, "description": "CDC-like kinase 2", "gene_symbol": "[\"Clk2\"]", "do": null }, { "gene_id": 12751, "description": "tripeptidyl peptidase I", "gene_symbol": "[\"Tpp1\"]", "do": "[{\"label\":\"neuronal ceroid lipofuscinosis 2\",\"id\":\"DOID:0110726\"}]" }, { "gene_id": 12752, "description": "CLN3 lysosomal/endosomal transmembrane protein, battenin", "gene_symbol": "[\"Cln3\"]", "do": "[{\"label\":\"neuronal ceroid lipofuscinosis 3\",\"id\":\"DOID:0110731\"}]" }, { "gene_id": 12753, "description": "clock circadian regulator", "gene_symbol": "[\"Clock\"]", "do": "[{\"label\":\"bipolar disorder\",\"id\":\"DOID:3312\"},{\"label\":\"diabetes mellitus\",\"id\":\"DOID:9351\"},{\"label\":\"sleep disorder\",\"id\":\"DOID:535\"}]" }, { "gene_id": 12759, "description": "clusterin", "gene_symbol": "[\"Clu\"]", "do": null }, { "gene_id": 12765, "description": "C-X-C motif chemokine receptor 2", "gene_symbol": "[\"Cxcr2\"]", "do": null }, { "gene_id": 12766, "description": "C-X-C motif chemokine receptor 3", "gene_symbol": "[\"Cxcr3\"]", "do": null }, { "gene_id": 12767, "description": "C-X-C motif chemokine receptor 4", "gene_symbol": "[\"Cxcr4\"]", "do": "[{\"label\":\"WHIM syndrome 1\",\"id\":\"DOID:0060591\"},{\"label\":\"cardiomyopathy\",\"id\":\"DOID:0050700\"},{\"label\":\"congestive heart failure\",\"id\":\"DOID:6000\"}]" }, { "gene_id": 12769, "description": "C-C motif chemokine receptor 9", "gene_symbol": "[\"Ccr9\"]", "do": null }, { "gene_id": 12773, "description": "C-C motif chemokine receptor 4", "gene_symbol": "[\"Ccr4\"]", "do": null }, { "gene_id": 12774, "description": "C-C motif chemokine receptor 5", "gene_symbol": "[\"Ccr5\"]", "do": "[{\"label\":\"Coronavirus infectious disease\",\"id\":\"DOID:0080599\"}]" }, { "gene_id": 12775, "description": "C-C motif chemokine receptor 7", "gene_symbol": "[\"Ccr7\"]", "do": "[{\"label\":\"Sjogren's syndrome\",\"id\":\"DOID:12894\"}]" }, { "gene_id": 12776, "description": "C-C motif chemokine receptor 8", "gene_symbol": "[\"Ccr8\"]", "do": null }, { "gene_id": 12778, "description": "atypical chemokine receptor 3", "gene_symbol": "[\"Ackr3\"]", "do": null }, { "gene_id": 12780, "description": "ATP-binding cassette, sub-family C member 2", "gene_symbol": "[\"Abcc2\"]", "do": null }, { "gene_id": 12788, "description": "cyclic nucleotide gated channel alpha 1", "gene_symbol": "[\"Cnga1\"]", "do": "[{\"label\":\"retinitis pigmentosa 49\",\"id\":\"DOID:0110377\"}]" }, { "gene_id": 12790, "description": "cyclic nucleotide gated channel alpha 3", "gene_symbol": "[\"Cnga3\"]", "do": "[{\"label\":\"achromatopsia 2\",\"id\":\"DOID:0110007\"}]" }, { "gene_id": 12798, "description": "calponin 2", "gene_symbol": "[\"Cnn2\"]", "do": null }, { "gene_id": 12799, "description": "2',3'-cyclic nucleotide 3' phosphodiesterase", "gene_symbol": "[\"Cnp\"]", "do": null }, { "gene_id": 12801, "description": "cannabinoid receptor 1", "gene_symbol": "[\"Cnr1\"]", "do": null }, { "gene_id": 12802, "description": "cannabinoid receptor 2", "gene_symbol": "[\"Cnr2\"]", "do": null }, { "gene_id": 12804, "description": "ciliary neurotrophic factor receptor", "gene_symbol": "[\"Cntfr\"]", "do": null }, { "gene_id": 12805, "description": "contactin 1", "gene_symbol": "[\"Cntn1\"]", "do": "[{\"label\":\"Compton-North congenital myopathy\",\"id\":\"DOID:0080101\"}]" }, { "gene_id": 12808, "description": "cordon-bleu WH2 repeat", "gene_symbol": "[\"Cobl\"]", "do": null }, { "gene_id": 12810, "description": "cochlin", "gene_symbol": "[\"Coch\"]", "do": "[{\"label\":\"autosomal dominant nonsyndromic deafness 9\",\"id\":\"DOID:0110593\"}]" }, { "gene_id": 12814, "description": "collagen, type XI, alpha 1", "gene_symbol": "[\"Col11a1\"]", "do": "[{\"label\":\"Stickler syndrome\",\"id\":\"DOID:0080046\"},{\"label\":\"osteoarthritis\",\"id\":\"DOID:8398\"}]" }, { "gene_id": 12815, "description": "collagen, type XI, alpha 2", "gene_symbol": "[\"Col11a2\"]", "do": "[{\"label\":\"Stickler syndrome\",\"id\":\"DOID:0080046\"},{\"label\":\"autosomal dominant nonsyndromic deafness 13\",\"id\":\"DOID:0110545\"},{\"label\":\"otospondylomegaepiphyseal dysplasia, autosomal recessive\",\"id\":\"DOID:0080026\"}]" }, { "gene_id": 12816, "description": "collagen, type XII, alpha 1", "gene_symbol": "[\"Col12a1\"]", "do": null }, { "gene_id": 12817, "description": "collagen, type XIII, alpha 1", "gene_symbol": "[\"Col13a1\"]", "do": "[{\"label\":\"congenital myasthenic syndrome 19\",\"id\":\"DOID:0110673\"}]" }, { "gene_id": 12818, "description": "collagen, type XIV, alpha 1", "gene_symbol": "[\"Col14a1\"]", "do": null }, { "gene_id": 12819, "description": "collagen, type XV, alpha 1", "gene_symbol": "[\"Col15a1\"]", "do": null }, { "gene_id": 12821, "description": "collagen, type XVII, alpha 1", "gene_symbol": "[\"Col17a1\"]", "do": "[{\"label\":\"junctional epidermolysis bullosa non-Herlitz type\",\"id\":\"DOID:0060738\"},{\"label\":\"junctional epidermolysis bullosa\",\"id\":\"DOID:3209\"}]" }, { "gene_id": 12822, "description": "collagen, type XVIII, alpha 1", "gene_symbol": "[\"Col18a1\"]", "do": "[{\"label\":\"pigment dispersion syndrome\",\"id\":\"DOID:0060680\"}]" }, { "gene_id": 12823, "description": "collagen, type XIX, alpha 1", "gene_symbol": "[\"Col19a1\"]", "do": null }, { "gene_id": 12824, "description": "collagen, type II, alpha 1", "gene_symbol": "[\"Col2a1\"]", "do": "[{\"label\":\"achondrogenesis type II\",\"id\":\"DOID:0080056\"},{\"label\":\"hypochondrogenesis\",\"id\":\"DOID:0080044\"},{\"label\":\"spondyloepimetaphyseal dysplasia\",\"id\":\"DOID:0080027\"},{\"label\":\"spondyloepiphyseal dysplasia congenita\",\"id\":\"DOID:14789\"}]" }, { "gene_id": 12825, "description": "collagen, type III, alpha 1", "gene_symbol": "[\"Col3a1\"]", "do": "[{\"label\":\"systemic scleroderma\",\"id\":\"DOID:418\"},{\"label\":\"vascular type Ehlers-Danlos syndrome\",\"id\":\"DOID:14756\"}]" }, { "gene_id": 12826, "description": "collagen, type IV, alpha 1", "gene_symbol": "[\"Col4a1\"]", "do": "[{\"label\":\"Walker-Warburg syndrome\",\"id\":\"DOID:0050560\"},{\"label\":\"brain small vessel disease 1\",\"id\":\"DOID:0090125\"},{\"label\":\"kidney disease\",\"id\":\"DOID:557\"},{\"label\":\"porencephaly\",\"id\":\"DOID:0060263\"}]" }, { "gene_id": 12827, "description": "collagen, type IV, alpha 2", "gene_symbol": "[\"Col4a2\"]", "do": null }, { "gene_id": 12828, "description": "collagen, type IV, alpha 3", "gene_symbol": "[\"Col4a3\"]", "do": "[{\"label\":\"Alport syndrome 2\",\"id\":\"DOID:0110033\"}]" }, { "gene_id": 12829, "description": "collagen, type IV, alpha 4", "gene_symbol": "[\"Col4a4\"]", "do": "[{\"label\":\"Alport syndrome 2\",\"id\":\"DOID:0110033\"}]" }, { "gene_id": 12830, "description": "collagen, type IV, alpha 5", "gene_symbol": "[\"Col4a5\"]", "do": null }, { "gene_id": 12831, "description": "collagen, type V, alpha 1", "gene_symbol": "[\"Col5a1\"]", "do": "[{\"label\":\"Ehlers-Danlos syndrome classic type 1\",\"id\":\"DOID:14720\"}]" }, { "gene_id": 12832, "description": "collagen, type V, alpha 2", "gene_symbol": "[\"Col5a2\"]", "do": "[{\"label\":\"Ehlers-Danlos syndrome classic type 1\",\"id\":\"DOID:14720\"}]" }, { "gene_id": 12833, "description": "collagen, type VI, alpha 1", "gene_symbol": "[\"Col6a1\"]", "do": "[{\"label\":\"Bethlem myopathy\",\"id\":\"DOID:0050663\"},{\"label\":\"Ullrich congenital muscular dystrophy\",\"id\":\"DOID:0050558\"}]" }, { "gene_id": 12834, "description": "collagen, type VI, alpha 2", "gene_symbol": "[\"Col6a2\"]", "do": null }, { "gene_id": 12835, "description": "collagen, type VI, alpha 3", "gene_symbol": "[\"Col6a3\"]", "do": "[{\"label\":\"Ullrich congenital muscular dystrophy\",\"id\":\"DOID:0050558\"},{\"label\":\"congenital muscular dystrophy\",\"id\":\"DOID:0050557\"}]" }, { "gene_id": 12836, "description": "collagen, type VII, alpha 1", "gene_symbol": "[\"Col7a1\"]", "do": "[{\"label\":\"recessive dystrophic epidermolysis bullosa\",\"id\":\"DOID:0060642\"}]" }, { "gene_id": 12842, "description": "collagen, type I, alpha 1", "gene_symbol": "[\"Col1a1\"]", "do": "[{\"label\":\"Ehlers-Danlos syndrome\",\"id\":\"DOID:13359\"},{\"label\":\"osteogenesis imperfecta type 1\",\"id\":\"DOID:0110334\"},{\"label\":\"osteogenesis imperfecta type 2\",\"id\":\"DOID:0110341\"},{\"label\":\"osteogenesis imperfecta type 3\",\"id\":\"DOID:0110339\"},{\"label\":\"osteogenesis imperfecta type 4\",\"id\":\"DOID:0110340\"},{\"label\":\"osteogenesis imperfecta\",\"id\":\"DOID:12347\"}]" }, { "gene_id": 12843, "description": "collagen, type I, alpha 2", "gene_symbol": "[\"Col1a2\"]", "do": "[{\"label\":\"osteogenesis imperfecta type 3\",\"id\":\"DOID:0110339\"},{\"label\":\"osteogenesis imperfecta\",\"id\":\"DOID:12347\"}]" }, { "gene_id": 12845, "description": "cartilage oligomeric matrix protein", "gene_symbol": "[\"Comp\"]", "do": "[{\"label\":\"multiple epiphyseal dysplasia\",\"id\":\"DOID:12721\"},{\"label\":\"pseudoachondroplasia\",\"id\":\"DOID:0080047\"}]" }, { "gene_id": 12846, "description": "catechol-O-methyltransferase", "gene_symbol": "[\"Comt\"]", "do": "[{\"label\":\"cognitive disorder\",\"id\":\"DOID:1561\"},{\"label\":\"pre-eclampsia\",\"id\":\"DOID:10591\"}]" }, { "gene_id": 12847, "description": "coatomer protein complex subunit alpha", "gene_symbol": "[\"Copa\"]", "do": "[{\"label\":\"autoimmune interstitial lung, joint, and kidney disease\",\"id\":\"DOID:0081242\"}]" }, { "gene_id": 12857, "description": "cytochrome c oxidase subunit 4I1", "gene_symbol": "[\"Cox4i1\"]", "do": null }, { "gene_id": 12858, "description": "cytochrome c oxidase subunit 5A", "gene_symbol": "[\"Cox5a\"]", "do": null }, { "gene_id": 12870, "description": "ceruloplasmin", "gene_symbol": "[\"Cp\"]", "do": "[{\"label\":\"aceruloplasminemia\",\"id\":\"DOID:0050711\"}]" }, { "gene_id": 12873, "description": "carboxypeptidase A3, mast cell", "gene_symbol": "[\"Cpa3\"]", "do": null }, { "gene_id": 12874, "description": "carboxypeptidase D", "gene_symbol": "[\"Cpd\"]", "do": null }, { "gene_id": 12876, "description": "carboxypeptidase E", "gene_symbol": "[\"Cpe\"]", "do": "[{\"label\":\"obesity\",\"id\":\"DOID:9970\"}]" }, { "gene_id": 12891, "description": "copine VI", "gene_symbol": "[\"Cpne6\"]", "do": null }, { "gene_id": 12892, "description": "coproporphyrinogen oxidase", "gene_symbol": "[\"Cpox\"]", "do": "[{\"label\":\"hereditary coproporphyria\",\"id\":\"DOID:13269\"}]" }, { "gene_id": 12894, "description": "carnitine palmitoyltransferase 1a, liver", "gene_symbol": "[\"Cpt1a\"]", "do": "[{\"label\":\"carnitine palmitoyltransferase I deficiency\",\"id\":\"DOID:0090129\"}]" }, { "gene_id": 12896, "description": "carnitine palmitoyltransferase 2", "gene_symbol": "[\"Cpt2\"]", "do": null }, { "gene_id": 12915, "description": "activating transcription factor 6 beta", "gene_symbol": "[\"Atf6b\"]", "do": null }, { "gene_id": 12919, "description": "corticotropin releasing hormone binding protein", "gene_symbol": "[\"Crhbp\"]", "do": null }, { "gene_id": 12921, "description": "corticotropin releasing hormone receptor 1", "gene_symbol": "[\"Crhr1\"]", "do": null }, { "gene_id": 12922, "description": "corticotropin releasing hormone receptor 2", "gene_symbol": "[\"Crhr2\"]", "do": null }, { "gene_id": 12927, "description": "breast cancer anti-estrogen resistance 1", "gene_symbol": "[\"Bcar1\"]", "do": null }, { "gene_id": 12929, "description": "Crk like proto-oncogene, adaptor protein", "gene_symbol": "[\"Crkl\"]", "do": "[{\"label\":\"DiGeorge syndrome\",\"id\":\"DOID:11198\"},{\"label\":\"velocardiofacial syndrome\",\"id\":\"DOID:12583\"}]" }, { "gene_id": 12931, "description": "cytokine receptor-like factor 1", "gene_symbol": "[\"Crlf1\"]", "do": null }, { "gene_id": 12933, "description": "collapsin response mediator protein 1", "gene_symbol": "[\"Crmp1\"]", "do": null }, { "gene_id": 12934, "description": "dihydropyrimidinase-like 2", "gene_symbol": "[\"Dpysl2\"]", "do": null }, { "gene_id": 12936, "description": "protocadherin alpha 4", "gene_symbol": "[\"Pcdha4\"]", "do": null }, { "gene_id": 12939, "description": "protocadherin alpha 7", "gene_symbol": "[\"Pcdha7\"]", "do": null }, { "gene_id": 12943, "description": "protocadherin alpha 10", "gene_symbol": "[\"Pcdha10\"]", "do": null }, { "gene_id": 12945, "description": "deleted in malignant brain tumors 1", "gene_symbol": "[\"Dmbt1\"]", "do": null }, { "gene_id": 12946, "description": "complement C3b/C4b receptor 1 like", "gene_symbol": "[\"Cr1l\"]", "do": null }, { "gene_id": 12950, "description": "hyaluronan and proteoglycan link protein 1", "gene_symbol": "[\"Hapln1\"]", "do": "[{\"label\":\"spondyloepiphyseal dysplasia congenita\",\"id\":\"DOID:14789\"}]" }, { "gene_id": 12952, "description": "cryptochrome circadian regulator 1", "gene_symbol": "[\"Cry1\"]", "do": null }, { "gene_id": 12953, "description": "cryptochrome circadian regulator 2", "gene_symbol": "[\"Cry2\"]", "do": null }, { "gene_id": 12954, "description": "crystallin, alpha A", "gene_symbol": "[\"Cryaa\"]", "do": "[{\"label\":\"cataract 9 multiple types\",\"id\":\"DOID:0110266\"}]" }, { "gene_id": 12955, "description": "crystallin, alpha B", "gene_symbol": "[\"Cryab\"]", "do": "[{\"label\":\"adult-onset myofibrillar myopathy 2A\",\"id\":\"DOID:0080093\"},{\"label\":\"cataract 16 multiple types\",\"id\":\"DOID:0110250\"}]" }, { "gene_id": 12972, "description": "crystallin, zeta", "gene_symbol": "[\"Cryz\"]", "do": null }, { "gene_id": 12974, "description": "citrate synthase", "gene_symbol": "[\"Cs\"]", "do": null }, { "gene_id": 12977, "description": "colony stimulating factor 1 (macrophage)", "gene_symbol": "[\"Csf1\"]", "do": "[{\"label\":\"osteopetrosis\",\"id\":\"DOID:13533\"}]" }, { "gene_id": 12978, "description": "colony stimulating factor 1 receptor", "gene_symbol": "[\"Csf1r\"]", "do": null }, { "gene_id": 12981, "description": "colony stimulating factor 2 (granulocyte-macrophage)", "gene_symbol": "[\"Csf2\"]", "do": "[{\"label\":\"pulmonary alveolar proteinosis\",\"id\":\"DOID:12120\"}]" }, { "gene_id": 12982, "description": "colony stimulating factor 2 receptor, alpha, low-affinity (granulocyte-macrophage)", "gene_symbol": "[\"Csf2ra\"]", "do": "[{\"label\":\"pulmonary alveolar proteinosis\",\"id\":\"DOID:12120\"}]" }, { "gene_id": 12983, "description": "colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage)", "gene_symbol": "[\"Csf2rb\"]", "do": "[{\"label\":\"pulmonary alveolar proteinosis\",\"id\":\"DOID:12120\"}]" }, { "gene_id": 12984, "description": "colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage)", "gene_symbol": "[\"Csf2rb2\"]", "do": null }, { "gene_id": 12985, "description": "colony stimulating factor 3 (granulocyte)", "gene_symbol": "[\"Csf3\"]", "do": null }, { "gene_id": 12986, "description": "colony stimulating factor 3 receptor", "gene_symbol": "[\"Csf3r\"]", "do": "[{\"label\":\"hereditary neutrophilia\",\"id\":\"DOID:0090120\"}]" }, { "gene_id": 12994, "description": "casein kappa", "gene_symbol": "[\"Csn3\"]", "do": null }, { "gene_id": 12995, "description": "casein kinase 2, alpha 1 polypeptide", "gene_symbol": "[\"Csnk2a1\"]", "do": null }, { "gene_id": 13000, "description": "casein kinase 2, alpha prime polypeptide", "gene_symbol": "[\"Csnk2a2\"]", "do": "[{\"label\":\"male infertility\",\"id\":\"DOID:12336\"}]" }, { "gene_id": 13003, "description": "versican", "gene_symbol": "[\"Vcan\"]", "do": null }, { "gene_id": 13004, "description": "neurocan", "gene_symbol": "[\"Ncan\"]", "do": null }, { "gene_id": 13007, "description": "cysteine and glycine-rich protein 1", "gene_symbol": "[\"Csrp1\"]", "do": null }, { "gene_id": 13010, "description": "cystatin C", "gene_symbol": "[\"Cst3\"]", "do": null }, { "gene_id": 13011, "description": "cystatin F (leukocystatin)", "gene_symbol": "[\"Cst7\"]", "do": null }, { "gene_id": 13012, "description": "cystatin 8 (cystatin-related epididymal spermatogenic)", "gene_symbol": "[\"Cst8\"]", "do": null }, { "gene_id": 13013, "description": "cystatin 9", "gene_symbol": "[\"Cst9\"]", "do": null }, { "gene_id": 13016, "description": "C-terminal binding protein 1", "gene_symbol": "[\"Ctbp1\"]", "do": null }, { "gene_id": 13017, "description": "C-terminal binding protein 2", "gene_symbol": "[\"Ctbp2\"]", "do": null }, { "gene_id": 13030, "description": "cathepsin B", "gene_symbol": "[\"Ctsb\"]", "do": null }, { "gene_id": 13032, "description": "cathepsin C", "gene_symbol": "[\"Ctsc\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 13033, "description": "cathepsin D", "gene_symbol": "[\"Ctsd\"]", "do": "[{\"label\":\"neuronal ceroid lipofuscinosis 10\",\"id\":\"DOID:0110725\"}]" }, { "gene_id": 13034, "description": "cathepsin E", "gene_symbol": "[\"Ctse\"]", "do": "[{\"label\":\"atopic dermatitis\",\"id\":\"DOID:3310\"}]" }, { "gene_id": 13035, "description": "cathepsin G", "gene_symbol": "[\"Ctsg\"]", "do": null }, { "gene_id": 13036, "description": "cathepsin H", "gene_symbol": "[\"Ctsh\"]", "do": null }, { "gene_id": 13038, "description": "cathepsin K", "gene_symbol": "[\"Ctsk\"]", "do": null }, { "gene_id": 13039, "description": "cathepsin L", "gene_symbol": "[\"Ctsl\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 13040, "description": "cathepsin S", "gene_symbol": "[\"Ctss\"]", "do": "[{\"label\":\"Duchenne muscular dystrophy\",\"id\":\"DOID:11723\"}]" }, { "gene_id": 13041, "description": "cathepsin W", "gene_symbol": "[\"Ctsw\"]", "do": null }, { "gene_id": 13043, "description": "cortactin", "gene_symbol": "[\"Cttn\"]", "do": null }, { "gene_id": 13047, "description": "cut-like homeobox 1", "gene_symbol": "[\"Cux1\"]", "do": null }, { "gene_id": 13052, "description": "coxsackie virus and adenovirus receptor", "gene_symbol": "[\"Cxadr\"]", "do": null }, { "gene_id": 13058, "description": "cytochrome b-245, beta polypeptide", "gene_symbol": "[\"Cybb\"]", "do": "[{\"label\":\"chronic granulomatous disease\",\"id\":\"DOID:3265\"},{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 13076, "description": "cytochrome P450, family 1, subfamily a, polypeptide 1", "gene_symbol": "[\"Cyp1a1\"]", "do": null }, { "gene_id": 13077, "description": "cytochrome P450, family 1, subfamily a, polypeptide 2", "gene_symbol": "[\"Cyp1a2\"]", "do": null }, { "gene_id": 13085, "description": "cytochrome P450, family 2, subfamily a, polypeptide 12", "gene_symbol": "[\"Cyp2a12\"]", "do": null }, { "gene_id": 13086, "description": "cytochrome P450, family 2, subfamily a, polypeptide 4", "gene_symbol": "[\"Cyp2a4\"]", "do": null }, { "gene_id": 13095, "description": "cytochrome P450, family 2, subfamily c, polypeptide 29", "gene_symbol": "[\"Cyp2c29\"]", "do": null }, { "gene_id": 13132, "description": "disabled 2, mitogen-responsive phosphoprotein", "gene_symbol": "[\"Dab2\"]", "do": null }, { "gene_id": 13136, "description": "CD55 molecule, decay accelerating factor for complement", "gene_symbol": "[\"Cd55\"]", "do": null }, { "gene_id": 13137, "description": "CD55 molecule, decay accelerating factor for complement B", "gene_symbol": "[\"Cd55b\"]", "do": null }, { "gene_id": 13138, "description": "dystroglycan 1", "gene_symbol": "[\"Dag1\"]", "do": "[{\"label\":\"autosomal recessive limb-girdle muscular dystrophy type 2P\",\"id\":\"DOID:0110293\"},{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"},{\"label\":\"lissencephaly\",\"id\":\"DOID:0050453\"}]" }, { "gene_id": 13162, "description": "solute carrier family 6 (neurotransmitter transporter, dopamine), member 3", "gene_symbol": "[\"Slc6a3\"]", "do": "[{\"label\":\"Gilles de la Tourette syndrome\",\"id\":\"DOID:11119\"},{\"label\":\"attention deficit hyperactivity disorder\",\"id\":\"DOID:1094\"},{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 13164, "description": "deleted in azoospermia-like", "gene_symbol": "[\"Dazl\"]", "do": null }, { "gene_id": 13166, "description": "dopamine beta hydroxylase", "gene_symbol": "[\"Dbh\"]", "do": "[{\"label\":\"dopamine beta-hydroxylase deficiency\",\"id\":\"DOID:0090145\"}]" }, { "gene_id": 13168, "description": "diazepam binding inhibitor-like 5", "gene_symbol": "[\"Dbil5\"]", "do": null }, { "gene_id": 13169, "description": "drebrin-like", "gene_symbol": "[\"Dbnl\"]", "do": null }, { "gene_id": 13172, "description": "developing brain homeobox 1", "gene_symbol": "[\"Dbx1\"]", "do": null }, { "gene_id": 13175, "description": "doublecortin-like kinase 1", "gene_symbol": "[\"Dclk1\"]", "do": null }, { "gene_id": 13176, "description": "DCC netrin 1 receptor", "gene_symbol": "[\"Dcc\"]", "do": null }, { "gene_id": 13179, "description": "decorin", "gene_symbol": "[\"Dcn\"]", "do": "[{\"label\":\"Ehlers-Danlos syndrome\",\"id\":\"DOID:13359\"},{\"label\":\"congenital stromal corneal dystrophy\",\"id\":\"DOID:0060445\"}]" }, { "gene_id": 13190, "description": "dopachrome tautomerase", "gene_symbol": "[\"Dct\"]", "do": null }, { "gene_id": 13191, "description": "dynactin 1", "gene_symbol": "[\"Dctn1\"]", "do": null }, { "gene_id": 13194, "description": "damage specific DNA binding protein 1", "gene_symbol": "[\"Ddb1\"]", "do": null }, { "gene_id": 13196, "description": "ArfGAP with SH3 domain, ankyrin repeat and PH domain1", "gene_symbol": "[\"Asap1\"]", "do": null }, { "gene_id": 13199, "description": "dendrin", "gene_symbol": "[\"Ddn\"]", "do": null }, { "gene_id": 13209, "description": "DEAD-box helicase 6", "gene_symbol": "[\"Ddx6\"]", "do": null }, { "gene_id": 13211, "description": "DExH-box helicase 9", "gene_symbol": "[\"Dhx9\"]", "do": null }, { "gene_id": 13218, "description": "defensin, alpha, 29", "gene_symbol": "[\"Defa29\"]", "do": null }, { "gene_id": 13340, "description": "solute carrier family 29 (nucleoside transporters), member 2", "gene_symbol": "[\"Slc29a2\"]", "do": null }, { "gene_id": 13346, "description": "desmin", "gene_symbol": "[\"Des\"]", "do": "[{\"label\":\"cardiomyopathy\",\"id\":\"DOID:0050700\"},{\"label\":\"dilated cardiomyopathy 1I\",\"id\":\"DOID:0110431\"},{\"label\":\"myofibrillar myopathy 1\",\"id\":\"DOID:0080092\"}]" }, { "gene_id": 13349, "description": "atypical chemokine receptor 1 (Duffy blood group)", "gene_symbol": "[\"Ackr1\"]", "do": null }, { "gene_id": 13356, "description": "DiGeorge syndrome critical region gene 2", "gene_symbol": "[\"Dgcr2\"]", "do": null }, { "gene_id": 13380, "description": "dickkopf WNT signaling pathway inhibitor 1", "gene_symbol": "[\"Dkk1\"]", "do": null }, { "gene_id": 13382, "description": "dihydrolipoamide dehydrogenase", "gene_symbol": "[\"Dld\"]", "do": null }, { "gene_id": 13383, "description": "discs large MAGUK scaffold protein 1", "gene_symbol": "[\"Dlg1\"]", "do": null }, { "gene_id": 13385, "description": "discs large MAGUK scaffold protein 4", "gene_symbol": "[\"Dlg4\"]", "do": "[{\"label\":\"Williams-Beuren syndrome\",\"id\":\"DOID:1928\"},{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 13386, "description": "delta like non-canonical Notch ligand 1", "gene_symbol": "[\"Dlk1\"]", "do": null }, { "gene_id": 13388, "description": "delta like canonical Notch ligand 1", "gene_symbol": "[\"Dll1\"]", "do": null }, { "gene_id": 13405, "description": "dystrophin, muscular dystrophy", "gene_symbol": "[\"Dmd\"]", "do": "[{\"label\":\"Becker muscular dystrophy\",\"id\":\"DOID:9883\"},{\"label\":\"Duchenne muscular dystrophy\",\"id\":\"DOID:11723\"}]" }, { "gene_id": 13406, "description": "dentin matrix protein 1", "gene_symbol": "[\"Dmp1\"]", "do": "[{\"label\":\"autosomal recessive hypophosphatemic rickets\",\"id\":\"DOID:0050949\"}]" }, { "gene_id": 13411, "description": "dynein, axonemal, heavy chain 11", "gene_symbol": "[\"Dnah11\"]", "do": "[{\"label\":\"Kartagener syndrome\",\"id\":\"DOID:0050144\"},{\"label\":\"atrioventricular septal defect\",\"id\":\"DOID:0050651\"},{\"label\":\"primary ciliary dyskinesia 7\",\"id\":\"DOID:0110605\"},{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 13417, "description": "dynein, axonemal, heavy chain 8", "gene_symbol": "[\"Dnah8\"]", "do": null }, { "gene_id": 13419, "description": "deoxyribonuclease I", "gene_symbol": "[\"Dnase1\"]", "do": "[{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 13423, "description": "deoxyribonuclease II alpha", "gene_symbol": "[\"Dnase2a\"]", "do": "[{\"label\":\"rheumatoid arthritis\",\"id\":\"DOID:7148\"}]" }, { "gene_id": 13424, "description": "dynein cytoplasmic 1 heavy chain 1", "gene_symbol": "[\"Dync1h1\"]", "do": "[{\"label\":\"Charcot-Marie-Tooth disease axonal type 2O\",\"id\":\"DOID:0110175\"}]" }, { "gene_id": 13426, "description": "dynein cytoplasmic 1 intermediate chain 1", "gene_symbol": "[\"Dync1i1\"]", "do": null }, { "gene_id": 13429, "description": "dynamin 1", "gene_symbol": "[\"Dnm1\"]", "do": "[{\"label\":\"generalized epilepsy\",\"id\":\"DOID:1827\"}]" }, { "gene_id": 13430, "description": "dynamin 2", "gene_symbol": "[\"Dnm2\"]", "do": "[{\"label\":\"centronuclear myopathy\",\"id\":\"DOID:14717\"},{\"label\":\"cystic kidney disease\",\"id\":\"DOID:2975\"},{\"label\":\"microcytic anemia\",\"id\":\"DOID:11252\"},{\"label\":\"myopathy\",\"id\":\"DOID:423\"}]" }, { "gene_id": 13433, "description": "DNA methyltransferase 1", "gene_symbol": "[\"Dnmt1\"]", "do": null }, { "gene_id": 13478, "description": "dolichyl-phosphate N-acetylglucosaminephosphotransferase 1", "gene_symbol": "[\"Dpagt1\"]", "do": null }, { "gene_id": 13479, "description": "dipeptidase 1", "gene_symbol": "[\"Dpep1\"]", "do": null }, { "gene_id": 13480, "description": "dolichyl-phosphate mannosyltransferase subunit 1, catalytic", "gene_symbol": "[\"Dpm1\"]", "do": null }, { "gene_id": 13481, "description": "dolichyl-phosphate mannosyltransferase subunit 2, regulatory", "gene_symbol": "[\"Dpm2\"]", "do": null }, { "gene_id": 13482, "description": "dipeptidylpeptidase 4", "gene_symbol": "[\"Dpp4\"]", "do": "[{\"label\":\"Middle East respiratory syndrome\",\"id\":\"DOID:0080642\"}]" }, { "gene_id": 13483, "description": "dipeptidylpeptidase 6", "gene_symbol": "[\"Dpp6\"]", "do": null }, { "gene_id": 13487, "description": "solute carrier family 26, member 3", "gene_symbol": "[\"Slc26a3\"]", "do": "[{\"label\":\"congenital secretory chloride diarrhea 1\",\"id\":\"DOID:0060296\"}]" }, { "gene_id": 13488, "description": "dopamine receptor D1", "gene_symbol": "[\"Drd1\"]", "do": null }, { "gene_id": 13489, "description": "dopamine receptor D2", "gene_symbol": "[\"Drd2\"]", "do": "[{\"label\":\"Parkinson's disease\",\"id\":\"DOID:14330\"},{\"label\":\"primary hyperaldosteronism\",\"id\":\"DOID:446\"}]" }, { "gene_id": 13490, "description": "dopamine receptor D3", "gene_symbol": "[\"Drd3\"]", "do": "[{\"label\":\"restless legs syndrome\",\"id\":\"DOID:0050425\"}]" }, { "gene_id": 13491, "description": "dopamine receptor D4", "gene_symbol": "[\"Drd4\"]", "do": null }, { "gene_id": 13492, "description": "dopamine receptor D5", "gene_symbol": "[\"Drd5\"]", "do": null }, { "gene_id": 13496, "description": "AT-rich interaction domain 3A", "gene_symbol": "[\"Arid3a\"]", "do": null }, { "gene_id": 13498, "description": "atrophin 1", "gene_symbol": "[\"Atn1\"]", "do": null }, { "gene_id": 13505, "description": "desmocollin 1", "gene_symbol": "[\"Dsc1\"]", "do": null }, { "gene_id": 13506, "description": "desmocollin 2", "gene_symbol": "[\"Dsc2\"]", "do": null }, { "gene_id": 13507, "description": "desmocollin 3", "gene_symbol": "[\"Dsc3\"]", "do": null }, { "gene_id": 13508, "description": "DS cell adhesion molecule", "gene_symbol": "[\"Dscam\"]", "do": null }, { "gene_id": 13510, "description": "desmoglein 1 alpha", "gene_symbol": "[\"Dsg1a\"]", "do": null }, { "gene_id": 13511, "description": "desmoglein 2", "gene_symbol": "[\"Dsg2\"]", "do": "[{\"label\":\"arrhythmogenic right ventricular cardiomyopathy\",\"id\":\"DOID:0050431\"},{\"label\":\"arrhythmogenic right ventricular dysplasia 10\",\"id\":\"DOID:0110081\"},{\"label\":\"intrinsic cardiomyopathy\",\"id\":\"DOID:0060036\"}]" }, { "gene_id": 13512, "description": "desmoglein 3", "gene_symbol": "[\"Dsg3\"]", "do": "[{\"label\":\"pemphigus vulgaris\",\"id\":\"DOID:0060851\"}]" }, { "gene_id": 13516, "description": "epiphycan", "gene_symbol": "[\"Epyc\"]", "do": null }, { "gene_id": 13518, "description": "dystonin", "gene_symbol": "[\"Dst\"]", "do": "[{\"label\":\"hereditary sensory and autonomic neuropathy type 6\",\"id\":\"DOID:0070151\"},{\"label\":\"hereditary sensory and autonomic neuropathy\",\"id\":\"DOID:0050548\"}]" }, { "gene_id": 13521, "description": "solute carrier family 26 (sulfate transporter), member 2", "gene_symbol": "[\"Slc26a2\"]", "do": "[{\"label\":\"diastrophic dysplasia\",\"id\":\"DOID:14687\"}]" }, { "gene_id": 13522, "description": "a disintegrin and metallopeptidase domain 28", "gene_symbol": "[\"Adam28\"]", "do": null }, { "gene_id": 13524, "description": "a disintegrin and metallopeptidase domain 18", "gene_symbol": "[\"Adam18\"]", "do": null }, { "gene_id": 13525, "description": "ADAM metallopeptidase domain 26A", "gene_symbol": "[\"Adam26a\"]", "do": null }, { "gene_id": 13526, "description": "ADAM metallopeptidase domain 24", "gene_symbol": "[\"Adam24\"]", "do": null }, { "gene_id": 13528, "description": "dystrobrevin, beta", "gene_symbol": "[\"Dtnb\"]", "do": null }, { "gene_id": 13542, "description": "dishevelled segment polarity protein 1", "gene_symbol": "[\"Dvl1\"]", "do": null }, { "gene_id": 13549, "description": "dual-specificity tyrosine phosphorylation regulated kinase 1b", "gene_symbol": "[\"Dyrk1b\"]", "do": null }, { "gene_id": 13586, "description": "eosinophil-associated, ribonuclease A family, member 1", "gene_symbol": "[\"Ear1\"]", "do": null }, { "gene_id": 13587, "description": "eosinophil-associated, ribonuclease A family, member 2", "gene_symbol": "[\"Ear2\"]", "do": null }, { "gene_id": 13590, "description": "left right determination factor 1", "gene_symbol": "[\"Lefty1\"]", "do": null }, { "gene_id": 13591, "description": "early B cell factor 1", "gene_symbol": "[\"Ebf1\"]", "do": "[{\"label\":\"lipodystrophy\",\"id\":\"DOID:811\"}]" }, { "gene_id": 13595, "description": "EBP cholestenol delta-isomerase", "gene_symbol": "[\"Ebp\"]", "do": "[{\"label\":\"X-linked chondrodysplasia punctata 1\",\"id\":\"DOID:0060292\"}]" }, { "gene_id": 13599, "description": "endothelin converting enzyme-like 1", "gene_symbol": "[\"Ecel1\"]", "do": "[{\"label\":\"distal arthrogryposis\",\"id\":\"DOID:0050646\"}]" }, { "gene_id": 13601, "description": "extracellular matrix protein 1", "gene_symbol": "[\"Ecm1\"]", "do": null }, { "gene_id": 13602, "description": "SPARC-like 1", "gene_symbol": "[\"Sparcl1\"]", "do": null }, { "gene_id": 13603, "description": "opsin 3", "gene_symbol": "[\"Opn3\"]", "do": null }, { "gene_id": 13607, "description": "ectodysplasin-A", "gene_symbol": "[\"Eda\"]", "do": "[{\"label\":\"hypohidrotic ectodermal dysplasia\",\"id\":\"DOID:14793\"}]" }, { "gene_id": 13608, "description": "ectodysplasin-A receptor", "gene_symbol": "[\"Edar\"]", "do": "[{\"label\":\"hypohidrotic ectodermal dysplasia\",\"id\":\"DOID:14793\"}]" }, { "gene_id": 13609, "description": "sphingosine-1-phosphate receptor 1", "gene_symbol": "[\"S1pr1\"]", "do": null }, { "gene_id": 13610, "description": "sphingosine-1-phosphate receptor 3", "gene_symbol": "[\"S1pr3\"]", "do": null }, { "gene_id": 13611, "description": "sphingosine-1-phosphate receptor 4", "gene_symbol": "[\"S1pr4\"]", "do": null }, { "gene_id": 13612, "description": "EGF-like repeats and discoidin I-like domains 3", "gene_symbol": "[\"Edil3\"]", "do": null }, { "gene_id": 13617, "description": "endothelin receptor type A", "gene_symbol": "[\"Ednra\"]", "do": "[{\"label\":\"mandibulofacial dysostosis with alopecia\",\"id\":\"DOID:0060365\"},{\"label\":\"velocardiofacial syndrome\",\"id\":\"DOID:12583\"}]" }, { "gene_id": 13618, "description": "endothelin receptor type B", "gene_symbol": "[\"Ednrb\"]", "do": "[{\"label\":\"Hirschsprung's disease\",\"id\":\"DOID:10487\"},{\"label\":\"Waardenburg syndrome type 4A\",\"id\":\"DOID:0110953\"}]" }, { "gene_id": 13619, "description": "polyhomeotic 1", "gene_symbol": "[\"Phc1\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"},{\"label\":\"tetralogy of Fallot\",\"id\":\"DOID:6419\"}]" }, { "gene_id": 13627, "description": "eukaryotic translation elongation factor 1 alpha 1", "gene_symbol": "[\"Eef1a1\"]", "do": null }, { "gene_id": 13628, "description": "eukaryotic translation elongation factor 1 alpha 2", "gene_symbol": "[\"Eef1a2\"]", "do": "[{\"label\":\"autosomal dominant intellectual developmental disorder 38\",\"id\":\"DOID:0070068\"}]" }, { "gene_id": 13629, "description": "eukaryotic translation elongation factor 2", "gene_symbol": "[\"Eef2\"]", "do": null }, { "gene_id": 13636, "description": "ephrin A1", "gene_symbol": "[\"Efna1\"]", "do": null }, { "gene_id": 13637, "description": "ephrin A2", "gene_symbol": "[\"Efna2\"]", "do": null }, { "gene_id": 13638, "description": "ephrin A3", "gene_symbol": "[\"Efna3\"]", "do": null }, { "gene_id": 13639, "description": "ephrin A4", "gene_symbol": "[\"Efna4\"]", "do": null }, { "gene_id": 13640, "description": "ephrin A5", "gene_symbol": "[\"Efna5\"]", "do": "[{\"label\":\"anencephaly\",\"id\":\"DOID:0060668\"}]" }, { "gene_id": 13641, "description": "ephrin B1", "gene_symbol": "[\"Efnb1\"]", "do": "[{\"label\":\"craniofrontonasal syndrome\",\"id\":\"DOID:14737\"}]" }, { "gene_id": 13642, "description": "ephrin B2", "gene_symbol": "[\"Efnb2\"]", "do": null }, { "gene_id": 13643, "description": "ephrin B3", "gene_symbol": "[\"Efnb3\"]", "do": "[{\"label\":\"movement disease\",\"id\":\"DOID:480\"}]" }, { "gene_id": 13645, "description": "epidermal growth factor", "gene_symbol": "[\"Egf\"]", "do": null }, { "gene_id": 13646, "description": "kallikrein 1-related peptidase b22", "gene_symbol": "[\"Klk1b22\"]", "do": null }, { "gene_id": 13647, "description": "epidermal growth factor binding protein type B", "gene_symbol": "[\"Egfbp2\"]", "do": null }, { "gene_id": 13648, "description": "kallikrein 1-related peptidase b9", "gene_symbol": "[\"Klk1b9\"]", "do": null }, { "gene_id": 13649, "description": "epidermal growth factor receptor", "gene_symbol": "[\"Egfr\"]", "do": "[{\"label\":\"Coronavirus infectious disease\",\"id\":\"DOID:0080599\"},{\"label\":\"aortic valve disease\",\"id\":\"DOID:62\"}]" }, { "gene_id": 13650, "description": "rhomboid 5 homolog 1", "gene_symbol": "[\"Rhbdf1\"]", "do": null }, { "gene_id": 13653, "description": "early growth response 1", "gene_symbol": "[\"Egr1\"]", "do": "[{\"label\":\"myelodysplastic syndrome\",\"id\":\"DOID:0050908\"}]" }, { "gene_id": 13654, "description": "early growth response 2", "gene_symbol": "[\"Egr2\"]", "do": null }, { "gene_id": 13655, "description": "early growth response 3", "gene_symbol": "[\"Egr3\"]", "do": null }, { "gene_id": 13665, "description": "eukaryotic translation initiation factor 2, subunit 1 alpha", "gene_symbol": "[\"Eif2s1\"]", "do": null }, { "gene_id": 13666, "description": "eukaryotic translation initiation factor 2 alpha kinase 3", "gene_symbol": "[\"Eif2ak3\"]", "do": "[{\"label\":\"Wolcott-Rallison syndrome\",\"id\":\"DOID:0090060\"}]" }, { "gene_id": 13667, "description": "eukaryotic translation initiation factor 2B, subunit 4 delta", "gene_symbol": "[\"Eif2b4\"]", "do": "[{\"label\":\"leukoencephalopathy with vanishing white matter\",\"id\":\"DOID:0060868\"}]" }, { "gene_id": 13669, "description": "eukaryotic translation initiation factor 3, subunit A", "gene_symbol": "[\"Eif3a\"]", "do": null }, { "gene_id": 13685, "description": "eukaryotic translation initiation factor 4E binding protein 1", "gene_symbol": "[\"Eif4ebp1\"]", "do": null }, { "gene_id": 13690, "description": "eukaryotic translation initiation factor 4, gamma 2", "gene_symbol": "[\"Eif4g2\"]", "do": null }, { "gene_id": 13709, "description": "E74 like ETS transcription factor 1", "gene_symbol": "[\"Elf1\"]", "do": null }, { "gene_id": 13712, "description": "ETS transcription factor ELK1", "gene_symbol": "[\"Elk1\"]", "do": null }, { "gene_id": 13722, "description": "aminoacyl tRNA synthetase complex-interacting multifunctional protein 1", "gene_symbol": "[\"Aimp1\"]", "do": null }, { "gene_id": 13723, "description": "embigin", "gene_symbol": "[\"Emb\"]", "do": null }, { "gene_id": 13726, "description": "emerin", "gene_symbol": "[\"Emd\"]", "do": null }, { "gene_id": 13728, "description": "MAP/microtubule affinity regulating kinase 2", "gene_symbol": "[\"Mark2\"]", "do": null }, { "gene_id": 13730, "description": "epithelial membrane protein 1", "gene_symbol": "[\"Emp1\"]", "do": null }, { "gene_id": 13731, "description": "epithelial membrane protein 2", "gene_symbol": "[\"Emp2\"]", "do": "[{\"label\":\"placental insufficiency\",\"id\":\"DOID:3891\"}]" }, { "gene_id": 13732, "description": "epithelial membrane protein 3", "gene_symbol": "[\"Emp3\"]", "do": null }, { "gene_id": 13733, "description": "adhesion G protein-coupled receptor E1", "gene_symbol": "[\"Adgre1\"]", "do": null }, { "gene_id": 13800, "description": "ENAH actin regulator", "gene_symbol": "[\"Enah\"]", "do": null }, { "gene_id": 13801, "description": "enamelin", "gene_symbol": "[\"Enam\"]", "do": "[{\"label\":\"amelogenesis imperfecta type 1B\",\"id\":\"DOID:0110052\"}]" }, { "gene_id": 13805, "description": "endoglin", "gene_symbol": "[\"Eng\"]", "do": "[{\"label\":\"arteriovenous malformations of the brain\",\"id\":\"DOID:0060688\"},{\"label\":\"hereditary hemorrhagic telangiectasia\",\"id\":\"DOID:1270\"}]" }, { "gene_id": 13806, "description": "enolase 1, alpha non-neuron", "gene_symbol": "[\"Eno1\"]", "do": null }, { "gene_id": 13807, "description": "enolase 2, gamma neuronal", "gene_symbol": "[\"Eno2\"]", "do": null }, { "gene_id": 13808, "description": "enolase 3, beta muscle", "gene_symbol": "[\"Eno3\"]", "do": null }, { "gene_id": 13809, "description": "glutamyl aminopeptidase", "gene_symbol": "[\"Enpep\"]", "do": null }, { "gene_id": 13821, "description": "erythrocyte membrane protein band 4.1 like 1", "gene_symbol": "[\"Epb41l1\"]", "do": null }, { "gene_id": 13822, "description": "erythrocyte membrane protein band 4.1 like 2", "gene_symbol": "[\"Epb41l2\"]", "do": null }, { "gene_id": 13823, "description": "erythrocyte membrane protein band 4.1 like 3", "gene_symbol": "[\"Epb41l3\"]", "do": null }, { "gene_id": 13824, "description": "erythrocyte membrane protein band 4.1 like 4a", "gene_symbol": "[\"Epb41l4a\"]", "do": null }, { "gene_id": 13829, "description": "dematin actin binding protein", "gene_symbol": "[\"Dmtn\"]", "do": null }, { "gene_id": 13830, "description": "stomatin", "gene_symbol": "[\"Stom\"]", "do": null }, { "gene_id": 13835, "description": "Eph receptor A1", "gene_symbol": "[\"Epha1\"]", "do": null }, { "gene_id": 13836, "description": "Eph receptor A2", "gene_symbol": "[\"Epha2\"]", "do": "[{\"label\":\"cataract 6 multiple types\",\"id\":\"DOID:0110229\"}]" }, { "gene_id": 13837, "description": "Eph receptor A3", "gene_symbol": "[\"Epha3\"]", "do": null }, { "gene_id": 13838, "description": "Eph receptor A4", "gene_symbol": "[\"Epha4\"]", "do": null }, { "gene_id": 13839, "description": "Eph receptor A5", "gene_symbol": "[\"Epha5\"]", "do": null }, { "gene_id": 13841, "description": "Eph receptor A7", "gene_symbol": "[\"Epha7\"]", "do": null }, { "gene_id": 13842, "description": "Eph receptor A8", "gene_symbol": "[\"Epha8\"]", "do": null }, { "gene_id": 13844, "description": "Eph receptor B2", "gene_symbol": "[\"Ephb2\"]", "do": null }, { "gene_id": 13845, "description": "Eph receptor B3", "gene_symbol": "[\"Ephb3\"]", "do": null }, { "gene_id": 13846, "description": "Eph receptor B4", "gene_symbol": "[\"Ephb4\"]", "do": "[{\"label\":\"cystic kidney disease\",\"id\":\"DOID:2975\"}]" }, { "gene_id": 13848, "description": "Eph receptor B6", "gene_symbol": "[\"Ephb6\"]", "do": null }, { "gene_id": 13849, "description": "epoxide hydrolase 1, microsomal", "gene_symbol": "[\"Ephx1\"]", "do": null }, { "gene_id": 13850, "description": "epoxide hydrolase 2, cytoplasmic", "gene_symbol": "[\"Ephx2\"]", "do": null }, { "gene_id": 13853, "description": "epilepsy, progressive myoclonic epilepsy, type 2 gene alpha", "gene_symbol": "[\"Epm2a\"]", "do": "[{\"label\":\"Lafora disease\",\"id\":\"DOID:3534\"}]" }, { "gene_id": 13854, "description": "epsin 1", "gene_symbol": "[\"Epn1\"]", "do": null }, { "gene_id": 13855, "description": "epsin 2", "gene_symbol": "[\"Epn2\"]", "do": null }, { "gene_id": 13856, "description": "erythropoietin", "gene_symbol": "[\"Epo\"]", "do": null }, { "gene_id": 13857, "description": "erythropoietin receptor", "gene_symbol": "[\"Epor\"]", "do": null }, { "gene_id": 13860, "description": "epidermal growth factor receptor pathway substrate 8", "gene_symbol": "[\"Eps8\"]", "do": null }, { "gene_id": 13861, "description": "eosinophil peroxidase", "gene_symbol": "[\"Epx\"]", "do": null }, { "gene_id": 13866, "description": "erb-b2 receptor tyrosine kinase 2", "gene_symbol": "[\"Erbb2\"]", "do": "[{\"label\":\"Hirschsprung's disease\",\"id\":\"DOID:10487\"},{\"label\":\"breast cancer\",\"id\":\"DOID:1612\"},{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 13867, "description": "erb-b2 receptor tyrosine kinase 3", "gene_symbol": "[\"Erbb3\"]", "do": null }, { "gene_id": 13869, "description": "erb-b2 receptor tyrosine kinase 4", "gene_symbol": "[\"Erbb4\"]", "do": null }, { "gene_id": 13874, "description": "epiregulin", "gene_symbol": "[\"Ereg\"]", "do": null }, { "gene_id": 13875, "description": "Ets2 repressor factor", "gene_symbol": "[\"Erf\"]", "do": null }, { "gene_id": 13884, "description": "carboxylesterase 1C", "gene_symbol": "[\"Ces1c\"]", "do": null }, { "gene_id": 13897, "description": "carboxylesterase 1E", "gene_symbol": "[\"Ces1e\"]", "do": null }, { "gene_id": 13909, "description": "carboxylesterase 3B", "gene_symbol": "[\"Ces3b\"]", "do": null }, { "gene_id": 13982, "description": "estrogen receptor 1 (alpha)", "gene_symbol": "[\"Esr1\"]", "do": "[{\"label\":\"breast cancer\",\"id\":\"DOID:1612\"}]" }, { "gene_id": 13983, "description": "estrogen receptor 2 (beta)", "gene_symbol": "[\"Esr2\"]", "do": null }, { "gene_id": 13992, "description": "KH domain containing, RNA binding, signal transduction associated 3", "gene_symbol": "[\"Khdrbs3\"]", "do": null }, { "gene_id": 14004, "description": "coiled-coil-helix-coiled-coil-helix domain containing 2", "gene_symbol": "[\"Chchd2\"]", "do": null }, { "gene_id": 14012, "description": "myelin protein zero-like 2", "gene_symbol": "[\"Mpzl2\"]", "do": null }, { "gene_id": 14017, "description": "ecotropic viral integration site 2a", "gene_symbol": "[\"Evi2a\"]", "do": null }, { "gene_id": 14030, "description": "Ewing sarcoma breakpoint region 1", "gene_symbol": "[\"Ewsr1\"]", "do": null }, { "gene_id": 14042, "description": "exostosin glycosyltransferase 1", "gene_symbol": "[\"Ext1\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"hereditary multiple exostoses\",\"id\":\"DOID:206\"}]" }, { "gene_id": 14043, "description": "exostosin glycosyltransferase 2", "gene_symbol": "[\"Ext2\"]", "do": "[{\"label\":\"hereditary multiple exostoses\",\"id\":\"DOID:206\"}]" }, { "gene_id": 14051, "description": "EYA transcriptional coactivator and phosphatase 4", "gene_symbol": "[\"Eya4\"]", "do": "[{\"label\":\"otitis media\",\"id\":\"DOID:10754\"}]" }, { "gene_id": 14056, "description": "enhancer of zeste 2 polycomb repressive complex 2 subunit", "gene_symbol": "[\"Ezh2\"]", "do": "[{\"label\":\"B-cell lymphoma\",\"id\":\"DOID:707\"},{\"label\":\"Weaver syndrome\",\"id\":\"DOID:14731\"},{\"label\":\"acute lymphoblastic leukemia\",\"id\":\"DOID:9952\"}]" }, { "gene_id": 14057, "description": "sideroflexin 1", "gene_symbol": "[\"Sfxn1\"]", "do": null }, { "gene_id": 14058, "description": "coagulation factor X", "gene_symbol": "[\"F10\"]", "do": null }, { "gene_id": 14060, "description": "coagulation factor XIII, beta subunit", "gene_symbol": "[\"F13b\"]", "do": null }, { "gene_id": 14061, "description": "coagulation factor II", "gene_symbol": "[\"F2\"]", "do": null }, { "gene_id": 14062, "description": "coagulation factor II thrombin receptor", "gene_symbol": "[\"F2r\"]", "do": null }, { "gene_id": 14063, "description": "F2R like trypsin receptor 1", "gene_symbol": "[\"F2rl1\"]", "do": null }, { "gene_id": 14064, "description": "coagulation factor II thrombin receptor like 2", "gene_symbol": "[\"F2rl2\"]", "do": null }, { "gene_id": 14065, "description": "F2R like thrombin or trypsin receptor 3", "gene_symbol": "[\"F2rl3\"]", "do": null }, { "gene_id": 14066, "description": "coagulation factor III, tissue factor", "gene_symbol": "[\"F3\"]", "do": null }, { "gene_id": 14067, "description": "coagulation factor V", "gene_symbol": "[\"F5\"]", "do": null }, { "gene_id": 14068, "description": "coagulation factor VII", "gene_symbol": "[\"F7\"]", "do": null }, { "gene_id": 14069, "description": "coagulation factor VIII", "gene_symbol": "[\"F8\"]", "do": "[{\"label\":\"factor VIII deficiency\",\"id\":\"DOID:12134\"}]" }, { "gene_id": 14071, "description": "coagulation factor IX", "gene_symbol": "[\"F9\"]", "do": "[{\"label\":\"hemophilia B\",\"id\":\"DOID:12259\"}]" }, { "gene_id": 14080, "description": "fatty acid binding protein 1, liver", "gene_symbol": "[\"Fabp1\"]", "do": null }, { "gene_id": 14081, "description": "acyl-CoA synthetase long-chain family member 1", "gene_symbol": "[\"Acsl1\"]", "do": "[{\"label\":\"cardiomyopathy\",\"id\":\"DOID:0050700\"}]" }, { "gene_id": 14084, "description": "Fas-associated factor 1", "gene_symbol": "[\"Faf1\"]", "do": null }, { "gene_id": 14086, "description": "fascin actin-bundling protein 1", "gene_symbol": "[\"Fscn1\"]", "do": null }, { "gene_id": 14087, "description": "Fanconi anemia, complementation group A", "gene_symbol": "[\"Fanca\"]", "do": "[{\"label\":\"Fanconi anemia complementation group A\",\"id\":\"DOID:0111095\"}]" }, { "gene_id": 14089, "description": "fibroblast activation protein", "gene_symbol": "[\"Fap\"]", "do": null }, { "gene_id": 14102, "description": "Fas cell surface death receptor", "gene_symbol": "[\"Fas\"]", "do": "[{\"label\":\"Sjogren's syndrome\",\"id\":\"DOID:12894\"},{\"label\":\"autoimmune lymphoproliferative syndrome\",\"id\":\"DOID:6688\"},{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 14103, "description": "Fas ligand", "gene_symbol": "[\"Fasl\"]", "do": "[{\"label\":\"autoimmune lymphoproliferative syndrome\",\"id\":\"DOID:6688\"},{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 14104, "description": "fatty acid synthase", "gene_symbol": "[\"Fasn\"]", "do": null }, { "gene_id": 14105, "description": "serine and arginine-rich splicing factor 10", "gene_symbol": "[\"Srsf10\"]", "do": null }, { "gene_id": 14107, "description": "FAT atypical cadherin 1", "gene_symbol": "[\"Fat1\"]", "do": "[{\"label\":\"facioscapulohumeral muscular dystrophy\",\"id\":\"DOID:11727\"},{\"label\":\"nephrotic syndrome\",\"id\":\"DOID:1184\"}]" }, { "gene_id": 14114, "description": "fibulin 1", "gene_symbol": "[\"Fbln1\"]", "do": null }, { "gene_id": 14115, "description": "fibulin 2", "gene_symbol": "[\"Fbln2\"]", "do": null }, { "gene_id": 14118, "description": "fibrillin 1", "gene_symbol": "[\"Fbn1\"]", "do": "[{\"label\":\"Marfan syndrome\",\"id\":\"DOID:14323\"},{\"label\":\"Weill-Marchesani syndrome\",\"id\":\"DOID:0050475\"},{\"label\":\"heart disease\",\"id\":\"DOID:114\"},{\"label\":\"systemic scleroderma\",\"id\":\"DOID:418\"}]" }, { "gene_id": 14119, "description": "fibrillin 2", "gene_symbol": "[\"Fbn2\"]", "do": "[{\"label\":\"distal arthrogryposis\",\"id\":\"DOID:0050646\"}]" }, { "gene_id": 14120, "description": "fructose bisphosphatase 2", "gene_symbol": "[\"Fbp2\"]", "do": null }, { "gene_id": 14121, "description": "fructose bisphosphatase 1", "gene_symbol": "[\"Fbp1\"]", "do": null }, { "gene_id": 14125, "description": "Fc receptor, IgE, high affinity I, alpha polypeptide", "gene_symbol": "[\"Fcer1a\"]", "do": null }, { "gene_id": 14128, "description": "Fc receptor, IgE, low affinity II, alpha polypeptide", "gene_symbol": "[\"Fcer2a\"]", "do": null }, { "gene_id": 14129, "description": "Fc receptor, IgG, high affinity I", "gene_symbol": "[\"Fcgr1\"]", "do": null }, { "gene_id": 14130, "description": "Fc receptor, IgG, low affinity IIb", "gene_symbol": "[\"Fcgr2b\"]", "do": "[{\"label\":\"malaria\",\"id\":\"DOID:12365\"},{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 14131, "description": "Fc receptor, IgG, low affinity III", "gene_symbol": "[\"Fcgr3\"]", "do": null }, { "gene_id": 14132, "description": "Fc fragment of IgG receptor and transporter", "gene_symbol": "[\"Fcgrt\"]", "do": null }, { "gene_id": 14133, "description": "ficolin A", "gene_symbol": "[\"Fcna\"]", "do": null }, { "gene_id": 14134, "description": "ficolin B", "gene_symbol": "[\"Fcnb\"]", "do": null }, { "gene_id": 14159, "description": "Fes proto-oncogene, tyrosine kinase", "gene_symbol": "[\"Fes\"]", "do": null }, { "gene_id": 14160, "description": "leucine rich repeat containing G protein coupled receptor 5", "gene_symbol": "[\"Lgr5\"]", "do": "[{\"label\":\"ankyloglossia\",\"id\":\"DOID:0060604\"}]" }, { "gene_id": 14161, "description": "fibrinogen alpha chain", "gene_symbol": "[\"Fga\"]", "do": null }, { "gene_id": 14165, "description": "fibroblast growth factor 10", "gene_symbol": "[\"Fgf10\"]", "do": "[{\"label\":\"intestinal atresia\",\"id\":\"DOID:10486\"},{\"label\":\"lacrimoauriculodentodigital syndrome 1\",\"id\":\"DOID:0050331\"}]" }, { "gene_id": 14171, "description": "fibroblast growth factor 17", "gene_symbol": "[\"Fgf17\"]", "do": null }, { "gene_id": 14172, "description": "fibroblast growth factor 18", "gene_symbol": "[\"Fgf18\"]", "do": null }, { "gene_id": 14176, "description": "fibroblast growth factor 5", "gene_symbol": "[\"Fgf5\"]", "do": null }, { "gene_id": 14177, "description": "fibroblast growth factor 6", "gene_symbol": "[\"Fgf6\"]", "do": null }, { "gene_id": 14178, "description": "fibroblast growth factor 7", "gene_symbol": "[\"Fgf7\"]", "do": null }, { "gene_id": 14179, "description": "fibroblast growth factor 8", "gene_symbol": "[\"Fgf8\"]", "do": "[{\"label\":\"DiGeorge syndrome\",\"id\":\"DOID:11198\"},{\"label\":\"tetralogy of Fallot\",\"id\":\"DOID:6419\"}]" }, { "gene_id": 14180, "description": "fibroblast growth factor 9", "gene_symbol": "[\"Fgf9\"]", "do": "[{\"label\":\"lung cancer\",\"id\":\"DOID:1324\"},{\"label\":\"multiple synostoses syndrome\",\"id\":\"DOID:0050794\"},{\"label\":\"pleuropulmonary blastoma\",\"id\":\"DOID:4769\"}]" }, { "gene_id": 14181, "description": "fibroblast growth factor binding protein 1", "gene_symbol": "[\"Fgfbp1\"]", "do": null }, { "gene_id": 14182, "description": "fibroblast growth factor receptor 1", "gene_symbol": "[\"Fgfr1\"]", "do": "[{\"label\":\"Pfeiffer syndrome\",\"id\":\"DOID:14705\"},{\"label\":\"otitis media\",\"id\":\"DOID:10754\"}]" }, { "gene_id": 14183, "description": "fibroblast growth factor receptor 2", "gene_symbol": "[\"Fgfr2\"]", "do": "[{\"label\":\"Beare-Stevenson cutis gyrata syndrome\",\"id\":\"DOID:0050660\"},{\"label\":\"Crouzon syndrome\",\"id\":\"DOID:2339\"},{\"label\":\"Pfeiffer syndrome\",\"id\":\"DOID:14705\"},{\"label\":\"acrocephalosyndactylia\",\"id\":\"DOID:12960\"},{\"label\":\"intestinal atresia\",\"id\":\"DOID:10486\"}]" }, { "gene_id": 14186, "description": "fibroblast growth factor receptor 4", "gene_symbol": "[\"Fgfr4\"]", "do": null }, { "gene_id": 14190, "description": "fibrinogen-like protein 2", "gene_symbol": "[\"Fgl2\"]", "do": "[{\"label\":\"autoimmune glomerulonephritis\",\"id\":\"DOID:0040094\"}]" }, { "gene_id": 14194, "description": "fumarate hydratase 1", "gene_symbol": "[\"Fh1\"]", "do": null }, { "gene_id": 14200, "description": "four and a half LIM domains 2", "gene_symbol": "[\"Fhl2\"]", "do": null }, { "gene_id": 14204, "description": "interleukin 4 induced 1", "gene_symbol": "[\"Il4i1\"]", "do": null }, { "gene_id": 14205, "description": "vascular endothelial growth factor D", "gene_symbol": "[\"Vegfd\"]", "do": null }, { "gene_id": 14218, "description": "SH3 and PX domains 2A", "gene_symbol": "[\"Sh3pxd2a\"]", "do": null }, { "gene_id": 14221, "description": "four jointed box 1", "gene_symbol": "[\"Fjx1\"]", "do": null }, { "gene_id": 14230, "description": "FK506 binding protein 10", "gene_symbol": "[\"Fkbp10\"]", "do": null }, { "gene_id": 14231, "description": "FK506 binding protein 7", "gene_symbol": "[\"Fkbp7\"]", "do": null }, { "gene_id": 14234, "description": "forkhead box C2", "gene_symbol": "[\"Foxc2\"]", "do": null }, { "gene_id": 14248, "description": "flightless I actin binding protein", "gene_symbol": "[\"Flii\"]", "do": null }, { "gene_id": 14254, "description": "FMS-like tyrosine kinase 1", "gene_symbol": "[\"Flt1\"]", "do": null }, { "gene_id": 14255, "description": "FMS-like tyrosine kinase 3", "gene_symbol": "[\"Flt3\"]", "do": "[{\"label\":\"acute myeloid leukemia\",\"id\":\"DOID:9119\"},{\"label\":\"juvenile myelomonocytic leukemia\",\"id\":\"DOID:0050458\"}]" }, { "gene_id": 14256, "description": "FMS-like tyrosine kinase 3 ligand", "gene_symbol": "[\"Flt3l\"]", "do": null }, { "gene_id": 14257, "description": "FMS-like tyrosine kinase 4", "gene_symbol": "[\"Flt4\"]", "do": "[{\"label\":\"hereditary lymphedema\",\"id\":\"DOID:0050580\"}]" }, { "gene_id": 14264, "description": "fibromodulin", "gene_symbol": "[\"Fmod\"]", "do": null }, { "gene_id": 14265, "description": "fragile X messenger ribonucleoprotein 1", "gene_symbol": "[\"Fmr1\"]", "do": null }, { "gene_id": 14268, "description": "fibronectin 1", "gene_symbol": "[\"Fn1\"]", "do": null }, { "gene_id": 14270, "description": "SLIT-ROBO Rho GTPase activating protein 2", "gene_symbol": "[\"Srgap2\"]", "do": null }, { "gene_id": 14272, "description": "farnesyltransferase, CAAX box, alpha", "gene_symbol": "[\"Fnta\"]", "do": null }, { "gene_id": 14275, "description": "folate receptor alpha", "gene_symbol": "[\"Folr1\"]", "do": null }, { "gene_id": 14276, "description": "folate receptor beta", "gene_symbol": "[\"Folr2\"]", "do": null }, { "gene_id": 14281, "description": "Fos proto-oncogene, AP-1 transcription factor subunit", "gene_symbol": "[\"Fos\"]", "do": null }, { "gene_id": 14284, "description": "fos-like antigen 2", "gene_symbol": "[\"Fosl2\"]", "do": "[{\"label\":\"idiopathic pulmonary fibrosis\",\"id\":\"DOID:0050156\"},{\"label\":\"systemic scleroderma\",\"id\":\"DOID:418\"}]" }, { "gene_id": 14289, "description": "formyl peptide receptor 2", "gene_symbol": "[\"Fpr2\"]", "do": null }, { "gene_id": 14290, "description": "formyl peptide receptor, related sequence 3", "gene_symbol": "[\"Fpr-rs3\"]", "do": null }, { "gene_id": 14291, "description": "formyl peptide receptor, related sequence 4", "gene_symbol": "[\"Fpr-rs4\"]", "do": null }, { "gene_id": 14293, "description": "formyl peptide receptor 1", "gene_symbol": "[\"Fpr1\"]", "do": null }, { "gene_id": 14294, "description": "formyl peptide receptor 3", "gene_symbol": "[\"Fpr3\"]", "do": null }, { "gene_id": 14308, "description": "follicle stimulating hormone beta", "gene_symbol": "[\"Fshb\"]", "do": null }, { "gene_id": 14309, "description": "follicle stimulating hormone receptor", "gene_symbol": "[\"Fshr\"]", "do": null }, { "gene_id": 14313, "description": "follistatin", "gene_symbol": "[\"Fst\"]", "do": "[{\"label\":\"restrictive dermopathy\",\"id\":\"DOID:0060762\"}]" }, { "gene_id": 14314, "description": "follistatin-like 1", "gene_symbol": "[\"Fstl1\"]", "do": "[{\"label\":\"pulmonary emphysema\",\"id\":\"DOID:9675\"}]" }, { "gene_id": 14319, "description": "ferritin heavy polypeptide 1", "gene_symbol": "[\"Fth1\"]", "do": null }, { "gene_id": 14343, "description": "fucosyltransferase 1", "gene_symbol": "[\"Fut1\"]", "do": null }, { "gene_id": 14344, "description": "fucosyltransferase 2", "gene_symbol": "[\"Fut2\"]", "do": null }, { "gene_id": 14345, "description": "fucosyltransferase 4", "gene_symbol": "[\"Fut4\"]", "do": null }, { "gene_id": 14347, "description": "fucosyltransferase 7", "gene_symbol": "[\"Fut7\"]", "do": null }, { "gene_id": 14348, "description": "fucosyltransferase 9", "gene_symbol": "[\"Fut9\"]", "do": null }, { "gene_id": 14359, "description": "FMR1 autosomal homolog 1", "gene_symbol": "[\"Fxr1\"]", "do": null }, { "gene_id": 14362, "description": "frizzled class receptor 1", "gene_symbol": "[\"Fzd1\"]", "do": null }, { "gene_id": 14365, "description": "frizzled class receptor 3", "gene_symbol": "[\"Fzd3\"]", "do": null }, { "gene_id": 14366, "description": "frizzled class receptor 4", "gene_symbol": "[\"Fzd4\"]", "do": "[{\"label\":\"Norrie disease\",\"id\":\"DOID:0060844\"},{\"label\":\"exudative vitreoretinopathy\",\"id\":\"DOID:0050535\"}]" }, { "gene_id": 14367, "description": "frizzled class receptor 5", "gene_symbol": "[\"Fzd5\"]", "do": null }, { "gene_id": 14368, "description": "frizzled class receptor 6", "gene_symbol": "[\"Fzd6\"]", "do": null }, { "gene_id": 14369, "description": "frizzled class receptor 7", "gene_symbol": "[\"Fzd7\"]", "do": null }, { "gene_id": 14370, "description": "frizzled class receptor 8", "gene_symbol": "[\"Fzd8\"]", "do": null }, { "gene_id": 14371, "description": "frizzled class receptor 9", "gene_symbol": "[\"Fzd9\"]", "do": "[{\"label\":\"Williams-Beuren syndrome\",\"id\":\"DOID:1928\"}]" }, { "gene_id": 14376, "description": "alpha glucosidase 2 alpha neutral subunit", "gene_symbol": "[\"Ganab\"]", "do": null }, { "gene_id": 14377, "description": "glucose-6-phosphatase catalytic subunit 1", "gene_symbol": "[\"G6pc1\"]", "do": "[{\"label\":\"glycogen storage disease Ia\",\"id\":\"DOID:2749\"}]" }, { "gene_id": 14378, "description": "glucose-6-phosphatase, catalytic, 2", "gene_symbol": "[\"G6pc2\"]", "do": "[{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 14380, "description": "glucose-6-phosphate dehydrogenase 2", "gene_symbol": "[\"G6pd2\"]", "do": null }, { "gene_id": 14381, "description": "glucose-6-phosphate dehydrogenase X-linked", "gene_symbol": "[\"G6pdx\"]", "do": "[{\"label\":\"favism\",\"id\":\"DOID:13628\"}]" }, { "gene_id": 14387, "description": "glucosidase, alpha, acid", "gene_symbol": "[\"Gaa\"]", "do": "[{\"label\":\"glycogen storage disease II\",\"id\":\"DOID:2752\"}]" }, { "gene_id": 14388, "description": "growth factor receptor bound protein 2-associated protein 1", "gene_symbol": "[\"Gab1\"]", "do": null }, { "gene_id": 14390, "description": "GA repeat binding protein, alpha", "gene_symbol": "[\"Gabpa\"]", "do": null }, { "gene_id": 14394, "description": "gamma-aminobutyric acid type A receptor subunit alpha 1", "gene_symbol": "[\"Gabra1\"]", "do": "[{\"label\":\"generalized epilepsy\",\"id\":\"DOID:1827\"}]" }, { "gene_id": 14395, "description": "gamma-aminobutyric acid type A receptor subunit alpha 2", "gene_symbol": "[\"Gabra2\"]", "do": null }, { "gene_id": 14396, "description": "gamma-aminobutyric acid type A receptor subunit alpha 3", "gene_symbol": "[\"Gabra3\"]", "do": null }, { "gene_id": 14397, "description": "gamma-aminobutyric acid type A receptor subunit alpha 4", "gene_symbol": "[\"Gabra4\"]", "do": null }, { "gene_id": 14399, "description": "gamma-aminobutyric acid type A receptor subunit alpha 6", "gene_symbol": "[\"Gabra6\"]", "do": null }, { "gene_id": 14400, "description": "gamma-aminobutyric acid type A receptor subunit beta 1", "gene_symbol": "[\"Gabrb1\"]", "do": null }, { "gene_id": 14401, "description": "gamma-aminobutyric acid type A receptor subunit beta 2", "gene_symbol": "[\"Gabrb2\"]", "do": null }, { "gene_id": 14402, "description": "GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3", "gene_symbol": "[\"Gabrb3\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 14403, "description": "gamma-aminobutyric acid (GABA) A receptor, subunit delta", "gene_symbol": "[\"Gabrd\"]", "do": "[{\"label\":\"postpartum depression\",\"id\":\"DOID:9478\"}]" }, { "gene_id": 14405, "description": "gamma-aminobutyric acid type A receptor subunit gamma 1", "gene_symbol": "[\"Gabrg1\"]", "do": "[{\"label\":\"trigeminal neuralgia\",\"id\":\"DOID:12098\"}]" }, { "gene_id": 14406, "description": "gamma-aminobutyric acid type A receptor, subunit gamma 2", "gene_symbol": "[\"Gabrg2\"]", "do": "[{\"label\":\"generalized epilepsy with febrile seizures plus\",\"id\":\"DOID:0060170\"}]" }, { "gene_id": 14407, "description": "gamma-aminobutyric acid type A receptor, subunit gamma 3", "gene_symbol": "[\"Gabrg3\"]", "do": null }, { "gene_id": 14408, "description": "gamma-aminobutyric acid type A receptor subunit rho 1", "gene_symbol": "[\"Gabrr1\"]", "do": null }, { "gene_id": 14409, "description": "gamma-aminobutyric acid type A receptor subunit rho 2", "gene_symbol": "[\"Gabrr2\"]", "do": null }, { "gene_id": 14411, "description": "solute carrier family 6 (neurotransmitter transporter, betaine/GABA), member 12", "gene_symbol": "[\"Slc6a12\"]", "do": null }, { "gene_id": 14412, "description": "solute carrier family 6 (neurotransmitter transporter, GABA), member 13", "gene_symbol": "[\"Slc6a13\"]", "do": null }, { "gene_id": 14415, "description": "glutamate decarboxylase 1", "gene_symbol": "[\"Gad1\"]", "do": null }, { "gene_id": 14420, "description": "galactosylceramidase", "gene_symbol": "[\"Galc\"]", "do": "[{\"label\":\"Krabbe disease\",\"id\":\"DOID:10587\"}]" }, { "gene_id": 14421, "description": "beta-1,4-N-acetyl-galactosaminyl transferase 1", "gene_symbol": "[\"B4galnt1\"]", "do": null }, { "gene_id": 14422, "description": "beta-1,4-N-acetyl-galactosaminyl transferase 2", "gene_symbol": "[\"B4galnt2\"]", "do": null }, { "gene_id": 14423, "description": "polypeptide N-acetylgalactosaminyltransferase 1", "gene_symbol": "[\"Galnt1\"]", "do": "[{\"label\":\"heart valve disease\",\"id\":\"DOID:4079\"}]" }, { "gene_id": 14425, "description": "polypeptide N-acetylgalactosaminyltransferase 3", "gene_symbol": "[\"Galnt3\"]", "do": "[{\"label\":\"hyperphosphatemic familial tumoral calcinosis\",\"id\":\"DOID:0111063\"}]" }, { "gene_id": 14426, "description": "polypeptide N-acetylgalactosaminyltransferase 4", "gene_symbol": "[\"Galnt4\"]", "do": null }, { "gene_id": 14427, "description": "galanin receptor 1", "gene_symbol": "[\"Galr1\"]", "do": null }, { "gene_id": 14428, "description": "galanin receptor 2", "gene_symbol": "[\"Galr2\"]", "do": null }, { "gene_id": 14429, "description": "galanin receptor 3", "gene_symbol": "[\"Galr3\"]", "do": null }, { "gene_id": 14430, "description": "galactose-1-phosphate uridyl transferase", "gene_symbol": "[\"Galt\"]", "do": "[{\"label\":\"galactosemia\",\"id\":\"DOID:9870\"}]" }, { "gene_id": 14432, "description": "growth associated protein 43", "gene_symbol": "[\"Gap43\"]", "do": null }, { "gene_id": 14433, "description": "glyceraldehyde-3-phosphate dehydrogenase", "gene_symbol": "[\"Gapdh\"]", "do": null }, { "gene_id": 14447, "description": "glyceraldehyde-3-phosphate dehydrogenase, spermatogenic", "gene_symbol": "[\"Gapdhs\"]", "do": null }, { "gene_id": 14451, "description": "growth arrest specific 1", "gene_symbol": "[\"Gas1\"]", "do": null }, { "gene_id": 14456, "description": "growth arrest specific 6", "gene_symbol": "[\"Gas6\"]", "do": null }, { "gene_id": 14463, "description": "GATA binding protein 4", "gene_symbol": "[\"Gata4\"]", "do": "[{\"label\":\"atrial heart septal defect 2\",\"id\":\"DOID:0110107\"},{\"label\":\"congenital diaphragmatic hernia\",\"id\":\"DOID:3827\"}]" }, { "gene_id": 14466, "description": "glucosylceramidase beta 1", "gene_symbol": "[\"Gba1\"]", "do": "[{\"label\":\"Gaucher's disease type I\",\"id\":\"DOID:0110957\"},{\"label\":\"Gaucher's disease type II\",\"id\":\"DOID:0110958\"},{\"label\":\"Gaucher's disease\",\"id\":\"DOID:1926\"}]" }, { "gene_id": 14473, "description": "vitamin D binding protein", "gene_symbol": "[\"Gc\"]", "do": null }, { "gene_id": 14479, "description": "ubiquitin specific peptidase 15", "gene_symbol": "[\"Usp15\"]", "do": null }, { "gene_id": 14527, "description": "glucagon receptor", "gene_symbol": "[\"Gcgr\"]", "do": "[{\"label\":\"Mahvash Disease\",\"id\":\"DOID:0112306\"}]" }, { "gene_id": 14534, "description": "K(lysine) acetyltransferase 2A", "gene_symbol": "[\"Kat2a\"]", "do": null }, { "gene_id": 14537, "description": "glucosaminyl (N-acetyl) transferase 1, core 2", "gene_symbol": "[\"Gcnt1\"]", "do": null }, { "gene_id": 14538, "description": "glucosaminyl (N-acetyl) transferase 2 (I blood group)", "gene_symbol": "[\"Gcnt2\"]", "do": null }, { "gene_id": 14539, "description": "opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan)", "gene_symbol": "[\"Opn1mw\"]", "do": "[{\"label\":\"blue cone monochromacy\",\"id\":\"DOID:0050679\"}]" }, { "gene_id": 14544, "description": "guanine deaminase", "gene_symbol": "[\"Gda\"]", "do": null }, { "gene_id": 14555, "description": "glycerol-3-phosphate dehydrogenase 1 (soluble)", "gene_symbol": "[\"Gpd1\"]", "do": null }, { "gene_id": 14559, "description": "growth differentiation factor 1", "gene_symbol": "[\"Gdf1\"]", "do": "[{\"label\":\"annular pancreas\",\"id\":\"DOID:0060850\"}]" }, { "gene_id": 14560, "description": "growth differentiation factor 10", "gene_symbol": "[\"Gdf10\"]", "do": null }, { "gene_id": 14561, "description": "growth differentiation factor 11", "gene_symbol": "[\"Gdf11\"]", "do": null }, { "gene_id": 14562, "description": "growth differentiation factor 3", "gene_symbol": "[\"Gdf3\"]", "do": null }, { "gene_id": 14563, "description": "growth differentiation factor 5", "gene_symbol": "[\"Gdf5\"]", "do": "[{\"label\":\"acromesomelic dysplasia, Grebe type\",\"id\":\"DOID:0080052\"},{\"label\":\"acromesomelic dysplasia, Hunter-Thompson type\",\"id\":\"DOID:0080051\"},{\"label\":\"brachydactyly type A1C\",\"id\":\"DOID:0110977\"},{\"label\":\"brachydactyly type A2\",\"id\":\"DOID:0110965\"},{\"label\":\"brachydactyly type C\",\"id\":\"DOID:0110970\"},{\"label\":\"fibular hypoplasia and complex brachydactyly\",\"id\":\"DOID:0050790\"},{\"label\":\"multiple synostoses syndrome\",\"id\":\"DOID:0050794\"},{\"label\":\"osteoarthritis\",\"id\":\"DOID:8398\"}]" }, { "gene_id": 14566, "description": "growth differentiation factor 9", "gene_symbol": "[\"Gdf9\"]", "do": null }, { "gene_id": 14567, "description": "GDP dissociation inhibitor 1", "gene_symbol": "[\"Gdi1\"]", "do": "[{\"label\":\"non-syndromic X-linked intellectual disability\",\"id\":\"DOID:0050776\"}]" }, { "gene_id": 14571, "description": "glycerol phosphate dehydrogenase 2, mitochondrial", "gene_symbol": "[\"Gpd2\"]", "do": null }, { "gene_id": 14573, "description": "glial cell line derived neurotrophic factor", "gene_symbol": "[\"Gdnf\"]", "do": "[{\"label\":\"Hirschsprung's disease\",\"id\":\"DOID:10487\"}]" }, { "gene_id": 14580, "description": "glial fibrillary acidic protein", "gene_symbol": "[\"Gfap\"]", "do": "[{\"label\":\"Alexander disease\",\"id\":\"DOID:4252\"}]" }, { "gene_id": 14583, "description": "glutamine fructose-6-phosphate transaminase 1", "gene_symbol": "[\"Gfpt1\"]", "do": "[{\"label\":\"congenital myasthenic syndrome 12\",\"id\":\"DOID:0110660\"}]" }, { "gene_id": 14585, "description": "glial cell line derived neurotrophic factor family receptor alpha 1", "gene_symbol": "[\"Gfra1\"]", "do": "[{\"label\":\"Hirschsprung's disease\",\"id\":\"DOID:10487\"}]" }, { "gene_id": 14586, "description": "glial cell line derived neurotrophic factor family receptor alpha 2", "gene_symbol": "[\"Gfra2\"]", "do": null }, { "gene_id": 14587, "description": "glial cell line derived neurotrophic factor family receptor alpha 3", "gene_symbol": "[\"Gfra3\"]", "do": null }, { "gene_id": 14588, "description": "glial cell line derived neurotrophic factor family receptor alpha 4", "gene_symbol": "[\"Gfra4\"]", "do": null }, { "gene_id": 14590, "description": "gamma-glutamyl hydrolase", "gene_symbol": "[\"Ggh\"]", "do": null }, { "gene_id": 14594, "description": "glycoprotein galactosyltransferase alpha 1, 3", "gene_symbol": "[\"Ggta1\"]", "do": null }, { "gene_id": 14595, "description": "UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1", "gene_symbol": "[\"B4galt1\"]", "do": "[{\"label\":\"IgA glomerulonephritis\",\"id\":\"DOID:2986\"},{\"label\":\"endocrine system disease\",\"id\":\"DOID:28\"}]" }, { "gene_id": 14598, "description": "gamma-glutamyltransferase 1", "gene_symbol": "[\"Ggt1\"]", "do": null }, { "gene_id": 14600, "description": "growth hormone receptor", "gene_symbol": "[\"Ghr\"]", "do": "[{\"label\":\"Laron syndrome\",\"id\":\"DOID:9521\"}]" }, { "gene_id": 14602, "description": "growth hormone releasing hormone receptor", "gene_symbol": "[\"Ghrhr\"]", "do": null }, { "gene_id": 14603, "description": "cobalamin binding intrinsic factor", "gene_symbol": "[\"Cblif\"]", "do": null }, { "gene_id": 14608, "description": "G protein-coupled receptor 83", "gene_symbol": "[\"Gpr83\"]", "do": null }, { "gene_id": 14609, "description": "gap junction protein, alpha 1", "gene_symbol": "[\"Gja1\"]", "do": "[{\"label\":\"oculodentodigital dysplasia\",\"id\":\"DOID:0060291\"}]" }, { "gene_id": 14623, "description": "gap junction protein, beta 6", "gene_symbol": "[\"Gjb6\"]", "do": "[{\"label\":\"Clouston syndrome\",\"id\":\"DOID:14693\"},{\"label\":\"autosomal recessive nonsyndromic deafness 1A\",\"id\":\"DOID:0110475\"}]" }, { "gene_id": 14626, "description": "glycerol kinase 2", "gene_symbol": "[\"Gk2\"]", "do": null }, { "gene_id": 14628, "description": "osteopetrosis associated transmembrane protein 1", "gene_symbol": "[\"Ostm1\"]", "do": "[{\"label\":\"autosomal recessive osteopetrosis 5\",\"id\":\"DOID:0110939\"}]" }, { "gene_id": 14629, "description": "glutamate-cysteine ligase, catalytic subunit", "gene_symbol": "[\"Gclc\"]", "do": "[{\"label\":\"cataract\",\"id\":\"DOID:83\"}]" }, { "gene_id": 14630, "description": "glutamate-cysteine ligase, modifier subunit", "gene_symbol": "[\"Gclm\"]", "do": null }, { "gene_id": 14633, "description": "GLI-Kruppel family member GLI2", "gene_symbol": "[\"Gli2\"]", "do": null }, { "gene_id": 14634, "description": "GLI-Kruppel family member GLI3", "gene_symbol": "[\"Gli3\"]", "do": "[{\"label\":\"Greig cephalopolysyndactyly syndrome\",\"id\":\"DOID:14761\"},{\"label\":\"Pallister-Hall syndrome\",\"id\":\"DOID:9248\"}]" }, { "gene_id": 14635, "description": "galactokinase 1", "gene_symbol": "[\"Galk1\"]", "do": null }, { "gene_id": 14645, "description": "glutamate-ammonia ligase", "gene_symbol": "[\"Glul\"]", "do": "[{\"label\":\"temporal lobe epilepsy\",\"id\":\"DOID:3328\"}]" }, { "gene_id": 14652, "description": "glucagon-like peptide 1 receptor", "gene_symbol": "[\"Glp1r\"]", "do": null }, { "gene_id": 14654, "description": "glycine receptor, alpha 1 subunit", "gene_symbol": "[\"Glra1\"]", "do": "[{\"label\":\"hyperekplexia 1\",\"id\":\"DOID:0060696\"},{\"label\":\"hyperekplexia\",\"id\":\"DOID:0060695\"}]" }, { "gene_id": 14657, "description": "glycine receptor, alpha 4 subunit", "gene_symbol": "[\"Glra4\"]", "do": null }, { "gene_id": 14658, "description": "glycine receptor, beta subunit", "gene_symbol": "[\"Glrb\"]", "do": "[{\"label\":\"hyperekplexia 2\",\"id\":\"DOID:0060697\"}]" }, { "gene_id": 14660, "description": "glutaminase", "gene_symbol": "[\"Gls\"]", "do": null }, { "gene_id": 14661, "description": "glutamate dehydrogenase 1", "gene_symbol": "[\"Glud1\"]", "do": null }, { "gene_id": 14663, "description": "glycosylation dependent cell adhesion molecule 1", "gene_symbol": "[\"Glycam1\"]", "do": null }, { "gene_id": 14667, "description": "GM2 ganglioside activator protein", "gene_symbol": "[\"Gm2a\"]", "do": "[{\"label\":\"GM2 gangliosidosis, AB variant\",\"id\":\"DOID:4795\"}]" }, { "gene_id": 14673, "description": "guanine nucleotide binding protein, alpha 12", "gene_symbol": "[\"Gna12\"]", "do": null }, { "gene_id": 14674, "description": "guanine nucleotide binding protein, alpha 13", "gene_symbol": "[\"Gna13\"]", "do": null }, { "gene_id": 14677, "description": "G protein subunit alpha i1", "gene_symbol": "[\"Gnai1\"]", "do": null }, { "gene_id": 14678, "description": "G protein subunit alpha i2", "gene_symbol": "[\"Gnai2\"]", "do": "[{\"label\":\"inflammatory bowel disease 12\",\"id\":\"DOID:0110887\"}]" }, { "gene_id": 14679, "description": "G protein subunit alpha i3", "gene_symbol": "[\"Gnai3\"]", "do": null }, { "gene_id": 14680, "description": "guanine nucleotide binding protein, alpha stimulating, olfactory type", "gene_symbol": "[\"Gnal\"]", "do": null }, { "gene_id": 14681, "description": "guanine nucleotide binding protein, alpha O", "gene_symbol": "[\"Gnao1\"]", "do": "[{\"label\":\"developmental and epileptic encephalopathy 17\",\"id\":\"DOID:0080450\"},{\"label\":\"neurodevelopmental disorder with involuntary movements\",\"id\":\"DOID:0112276\"}]" }, { "gene_id": 14683, "description": "GNAS complex locus", "gene_symbol": "[\"Gnas\"]", "do": "[{\"label\":\"pseudohypoparathyroidism type 1A\",\"id\":\"DOID:0080053\"},{\"label\":\"pseudohypoparathyroidism\",\"id\":\"DOID:4184\"},{\"label\":\"pseudopseudohypoparathyroidism\",\"id\":\"DOID:4183\"},{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 14688, "description": "guanine nucleotide binding protein (G protein), beta 1", "gene_symbol": "[\"Gnb1\"]", "do": null }, { "gene_id": 14694, "description": "receptor for activated C kinase 1", "gene_symbol": "[\"Rack1\"]", "do": null }, { "gene_id": 14705, "description": "BSCL2 lipid droplet biogenesis associated, seipin", "gene_symbol": "[\"Bscl2\"]", "do": "[{\"label\":\"congenital generalized lipodystrophy type 2\",\"id\":\"DOID:0111136\"},{\"label\":\"male infertility\",\"id\":\"DOID:12336\"}]" }, { "gene_id": 14711, "description": "glycine N-methyltransferase", "gene_symbol": "[\"Gnmt\"]", "do": "[{\"label\":\"glycine N-methyltransferase deficiency\",\"id\":\"DOID:0111037\"},{\"label\":\"hepatocellular carcinoma\",\"id\":\"DOID:684\"}]" }, { "gene_id": 14715, "description": "gonadotropin releasing hormone receptor", "gene_symbol": "[\"Gnrhr\"]", "do": "[{\"label\":\"hypogonadotropic hypogonadism 7 with or without anosmia\",\"id\":\"DOID:0090078\"}]" }, { "gene_id": 14718, "description": "glutamic-oxaloacetic transaminase 1, soluble", "gene_symbol": "[\"Got1\"]", "do": null }, { "gene_id": 14723, "description": "glycoprotein 1b, alpha polypeptide", "gene_symbol": "[\"Gp1ba\"]", "do": "[{\"label\":\"Bernard-Soulier syndrome\",\"id\":\"DOID:2217\"}]" }, { "gene_id": 14724, "description": "glycoprotein Ib, beta polypeptide", "gene_symbol": "[\"Gp1bb\"]", "do": "[{\"label\":\"Bernard-Soulier syndrome\",\"id\":\"DOID:2217\"}]" }, { "gene_id": 14725, "description": "low density lipoprotein receptor-related protein 2", "gene_symbol": "[\"Lrp2\"]", "do": "[{\"label\":\"Donnai-Barrow syndrome\",\"id\":\"DOID:0090144\"},{\"label\":\"Fanconi syndrome\",\"id\":\"DOID:1062\"},{\"label\":\"degenerative myopia\",\"id\":\"DOID:11829\"}]" }, { "gene_id": 14726, "description": "podoplanin", "gene_symbol": "[\"Pdpn\"]", "do": null }, { "gene_id": 14727, "description": "leukocyte immunoglobulin-like receptor, subfamily B, member 4B", "gene_symbol": "[\"Lilrb4b\"]", "do": null }, { "gene_id": 14728, "description": "leukocyte immunoglobulin-like receptor, subfamily B, member 4A", "gene_symbol": "[\"Lilrb4a\"]", "do": null }, { "gene_id": 14729, "description": "glycoprotein 5 platelet", "gene_symbol": "[\"Gp5\"]", "do": null }, { "gene_id": 14731, "description": "GPI anchor attachment protein 1", "gene_symbol": "[\"Gpaa1\"]", "do": null }, { "gene_id": 14733, "description": "glypican 1", "gene_symbol": "[\"Gpc1\"]", "do": null }, { "gene_id": 14734, "description": "glypican 3", "gene_symbol": "[\"Gpc3\"]", "do": "[{\"label\":\"Simpson-Golabi-Behmel syndrome type 1\",\"id\":\"DOID:0060248\"}]" }, { "gene_id": 14735, "description": "glypican 4", "gene_symbol": "[\"Gpc4\"]", "do": null }, { "gene_id": 14738, "description": "G-protein coupled receptor 12", "gene_symbol": "[\"Gpr12\"]", "do": "[{\"label\":\"obesity\",\"id\":\"DOID:9970\"}]" }, { "gene_id": 14739, "description": "sphingosine-1-phosphate receptor 2", "gene_symbol": "[\"S1pr2\"]", "do": "[{\"label\":\"autosomal recessive nonsyndromic deafness 68\",\"id\":\"DOID:0110519\"},{\"label\":\"non-Hodgkin lymphoma\",\"id\":\"DOID:0060060\"}]" }, { "gene_id": 14744, "description": "G-protein coupled receptor 65", "gene_symbol": "[\"Gpr65\"]", "do": null }, { "gene_id": 14745, "description": "lysophosphatidic acid receptor 1", "gene_symbol": "[\"Lpar1\"]", "do": null }, { "gene_id": 14747, "description": "chemerin chemokine-like receptor 1", "gene_symbol": "[\"Cmklr1\"]", "do": null }, { "gene_id": 14748, "description": "G-protein coupled receptor 3", "gene_symbol": "[\"Gpr3\"]", "do": null }, { "gene_id": 14751, "description": "glucose-6-phosphate isomerase 1", "gene_symbol": "[\"Gpi1\"]", "do": "[{\"label\":\"congenital nonspherocytic hemolytic anemia\",\"id\":\"DOID:2861\"}]" }, { "gene_id": 14756, "description": "glycosylphosphatidylinositol specific phospholipase D1", "gene_symbol": "[\"Gpld1\"]", "do": null }, { "gene_id": 14758, "description": "glycoprotein m6b", "gene_symbol": "[\"Gpm6b\"]", "do": null }, { "gene_id": 14760, "description": "G protein-coupled receptor 19", "gene_symbol": "[\"Gpr19\"]", "do": null }, { "gene_id": 14761, "description": "G protein-coupled receptor 27", "gene_symbol": "[\"Gpr27\"]", "do": null }, { "gene_id": 14762, "description": "G protein-coupled receptor 33", "gene_symbol": "[\"Gpr33\"]", "do": null }, { "gene_id": 14763, "description": "G protein-coupled receptor 37", "gene_symbol": "[\"Gpr37\"]", "do": null }, { "gene_id": 14764, "description": "prostaglandin D2 receptor 2", "gene_symbol": "[\"Ptgdr2\"]", "do": null }, { "gene_id": 14765, "description": "G-protein-coupled receptor 50", "gene_symbol": "[\"Gpr50\"]", "do": null }, { "gene_id": 14766, "description": "adhesion G protein-coupled receptor G1", "gene_symbol": "[\"Adgrg1\"]", "do": null }, { "gene_id": 14767, "description": "neuromedin U receptor 1", "gene_symbol": "[\"Nmur1\"]", "do": null }, { "gene_id": 14768, "description": "LanC (bacterial lantibiotic synthetase component C)-like 1", "gene_symbol": "[\"Lancl1\"]", "do": null }, { "gene_id": 14775, "description": "glutathione peroxidase 1", "gene_symbol": "[\"Gpx1\"]", "do": null }, { "gene_id": 14782, "description": "glutathione reductase", "gene_symbol": "[\"Gsr\"]", "do": null }, { "gene_id": 14783, "description": "growth factor receptor bound protein 10", "gene_symbol": "[\"Grb10\"]", "do": null }, { "gene_id": 14788, "description": "G protein-coupled receptor 162", "gene_symbol": "[\"Gpr162\"]", "do": null }, { "gene_id": 14789, "description": "prolyl 3-hydroxylase 3", "gene_symbol": "[\"P3h3\"]", "do": null }, { "gene_id": 14790, "description": "gene rich cluster, C10 gene", "gene_symbol": "[\"Grcc10\"]", "do": null }, { "gene_id": 14792, "description": "lysophosphatidylcholine acyltransferase 3", "gene_symbol": "[\"Lpcat3\"]", "do": null }, { "gene_id": 14799, "description": "glutamate receptor, ionotropic, AMPA1 (alpha 1)", "gene_symbol": "[\"Gria1\"]", "do": "[{\"label\":\"schizoaffective disorder\",\"id\":\"DOID:5418\"}]" }, { "gene_id": 14800, "description": "glutamate receptor, ionotropic, AMPA2 (alpha 2)", "gene_symbol": "[\"Gria2\"]", "do": null }, { "gene_id": 14802, "description": "glutamate receptor, ionotropic, AMPA4 (alpha 4)", "gene_symbol": "[\"Gria4\"]", "do": null }, { "gene_id": 14803, "description": "glutamate receptor, ionotropic, delta 1", "gene_symbol": "[\"Grid1\"]", "do": null }, { "gene_id": 14804, "description": "glutamate receptor, ionotropic, delta 2", "gene_symbol": "[\"Grid2\"]", "do": "[{\"label\":\"autosomal recessive spinocerebellar ataxia 18\",\"id\":\"DOID:0080042\"}]" }, { "gene_id": 14805, "description": "glutamate receptor, ionotropic, kainate 1", "gene_symbol": "[\"Grik1\"]", "do": null }, { "gene_id": 14806, "description": "glutamate receptor, ionotropic, kainate 2 (beta 2)", "gene_symbol": "[\"Grik2\"]", "do": null }, { "gene_id": 14807, "description": "glutamate receptor, ionotropic, kainate 3", "gene_symbol": "[\"Grik3\"]", "do": null }, { "gene_id": 14809, "description": "glutamate receptor, ionotropic, kainate 5 (gamma 2)", "gene_symbol": "[\"Grik5\"]", "do": null }, { "gene_id": 14810, "description": "glutamate receptor, ionotropic, NMDA1 (zeta 1)", "gene_symbol": "[\"Grin1\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 14811, "description": "glutamate receptor, ionotropic, NMDA2A (epsilon 1)", "gene_symbol": "[\"Grin2a\"]", "do": null }, { "gene_id": 14812, "description": "glutamate receptor, ionotropic, NMDA2B (epsilon 2)", "gene_symbol": "[\"Grin2b\"]", "do": null }, { "gene_id": 14813, "description": "glutamate receptor, ionotropic, NMDA2C (epsilon 3)", "gene_symbol": "[\"Grin2c\"]", "do": null }, { "gene_id": 14814, "description": "glutamate receptor, ionotropic, NMDA2D (epsilon 4)", "gene_symbol": "[\"Grin2d\"]", "do": null }, { "gene_id": 14815, "description": "nuclear receptor subfamily 3, group C, member 1", "gene_symbol": "[\"Nr3c1\"]", "do": "[{\"label\":\"primary hyperaldosteronism\",\"id\":\"DOID:446\"}]" }, { "gene_id": 14816, "description": "glutamate receptor, metabotropic 1", "gene_symbol": "[\"Grm1\"]", "do": "[{\"label\":\"autosomal recessive spinocerebellar ataxia 13\",\"id\":\"DOID:0080062\"},{\"label\":\"skin melanoma\",\"id\":\"DOID:8923\"},{\"label\":\"uveal melanoma\",\"id\":\"DOID:6039\"}]" }, { "gene_id": 14823, "description": "glutamate receptor, metabotropic 8", "gene_symbol": "[\"Grm8\"]", "do": null }, { "gene_id": 14824, "description": "granulin", "gene_symbol": "[\"Grn\"]", "do": "[{\"label\":\"frontotemporal dementia 2\",\"id\":\"DOID:0060672\"},{\"label\":\"nephrogenic diabetes insipidus\",\"id\":\"DOID:12387\"}]" }, { "gene_id": 14827, "description": "protein disulfide isomerase associated 3", "gene_symbol": "[\"Pdia3\"]", "do": null }, { "gene_id": 14828, "description": "heat shock protein family A (Hsp70) member 5", "gene_symbol": "[\"Hspa5\"]", "do": null }, { "gene_id": 14829, "description": "gastrin releasing peptide receptor", "gene_symbol": "[\"Grpr\"]", "do": null }, { "gene_id": 14854, "description": "glutathione synthetase", "gene_symbol": "[\"Gss\"]", "do": null }, { "gene_id": 14873, "description": "glutathione S-transferase omega 1", "gene_symbol": "[\"Gsto1\"]", "do": null }, { "gene_id": 14897, "description": "thyroid hormone receptor interactor 12", "gene_symbol": "[\"Trip12\"]", "do": null }, { "gene_id": 14904, "description": "GTP binding protein 1", "gene_symbol": "[\"Gtpbp1\"]", "do": null }, { "gene_id": 14917, "description": "guanylate cyclase 2c", "gene_symbol": "[\"Gucy2c\"]", "do": "[{\"label\":\"abdominal obesity-metabolic syndrome\",\"id\":\"DOID:0060611\"},{\"label\":\"obesity\",\"id\":\"DOID:9970\"}]" }, { "gene_id": 14919, "description": "guanylate cyclase 2e", "gene_symbol": "[\"Gucy2e\"]", "do": "[{\"label\":\"Leber congenital amaurosis 1\",\"id\":\"DOID:0110078\"},{\"label\":\"cone-rod dystrophy 6\",\"id\":\"DOID:0111011\"}]" }, { "gene_id": 14924, "description": "membrane associated guanylate kinase, WW and PDZ domain containing 1", "gene_symbol": "[\"Magi1\"]", "do": null }, { "gene_id": 14933, "description": "glycerol kinase", "gene_symbol": "[\"Gk\"]", "do": "[{\"label\":\"glycerol kinase deficiency\",\"id\":\"DOID:0060363\"}]" }, { "gene_id": 14934, "description": "glycophorin A", "gene_symbol": "[\"Gypa\"]", "do": null }, { "gene_id": 14936, "description": "glycogen synthase 1, muscle", "gene_symbol": "[\"Gys1\"]", "do": null }, { "gene_id": 14938, "description": "granzyme A", "gene_symbol": "[\"Gzma\"]", "do": null }, { "gene_id": 14939, "description": "granzyme B", "gene_symbol": "[\"Gzmb\"]", "do": null }, { "gene_id": 14941, "description": "granzyme D", "gene_symbol": "[\"Gzmd\"]", "do": null }, { "gene_id": 14942, "description": "granzyme E", "gene_symbol": "[\"Gzme\"]", "do": null }, { "gene_id": 14943, "description": "granzyme F", "gene_symbol": "[\"Gzmf\"]", "do": null }, { "gene_id": 14944, "description": "granzyme G", "gene_symbol": "[\"Gzmg\"]", "do": null }, { "gene_id": 14950, "description": "histocompatibility 13", "gene_symbol": "[\"H13\"]", "do": null }, { "gene_id": 14958, "description": "H1.0 linker histone", "gene_symbol": "[\"H1f0\"]", "do": null }, { "gene_id": 14960, "description": "histocompatibility 2, class II antigen A, alpha", "gene_symbol": "[\"H2-Aa\"]", "do": null }, { "gene_id": 14961, "description": "histocompatibility 2, class II antigen A, beta 1", "gene_symbol": "[\"H2-Ab1\"]", "do": null }, { "gene_id": 14962, "description": "complement factor B", "gene_symbol": "[\"Cfb\"]", "do": null }, { "gene_id": 14963, "description": "histocompatibility 2, blastocyst", "gene_symbol": "[\"H2-Bl\"]", "do": null }, { "gene_id": 14964, "description": "histocompatibility 2, D region locus 1", "gene_symbol": "[\"H2-D1\"]", "do": null }, { "gene_id": 14969, "description": "histocompatibility 2, class II antigen E beta", "gene_symbol": "[\"H2-Eb1\"]", "do": null }, { "gene_id": 14972, "description": "histocompatibility 2, K1, K region", "gene_symbol": "[\"H2-K1\"]", "do": "[{\"label\":\"myositis\",\"id\":\"DOID:633\"}]" }, { "gene_id": 14990, "description": "histocompatibility 2, M region locus 2", "gene_symbol": "[\"H2-M2\"]", "do": null }, { "gene_id": 14991, "description": "histocompatibility 2, M region locus 3", "gene_symbol": "[\"H2-M3\"]", "do": null }, { "gene_id": 14999, "description": "histocompatibility 2, class II, locus Mb1", "gene_symbol": "[\"H2-DMb1\"]", "do": null }, { "gene_id": 15006, "description": "histocompatibility 2, Q region locus 1", "gene_symbol": "[\"H2-Q1\"]", "do": null }, { "gene_id": 15007, "description": "histocompatibility 2, Q region locus 10", "gene_symbol": "[\"H2-Q10\"]", "do": null }, { "gene_id": 15013, "description": "histocompatibility 2, Q region locus 2", "gene_symbol": "[\"H2-Q2\"]", "do": null }, { "gene_id": 15015, "description": "histocompatibility 2, Q region locus 4", "gene_symbol": "[\"H2-Q4\"]", "do": null }, { "gene_id": 15018, "description": "histocompatibility 2, Q region locus 7", "gene_symbol": "[\"H2-Q7\"]", "do": null }, { "gene_id": 15040, "description": "histocompatibility 2, T region locus 23", "gene_symbol": "[\"H2-T23\"]", "do": null }, { "gene_id": 15042, "description": "histocompatibility 2, T region locus 24", "gene_symbol": "[\"H2-T24\"]", "do": null }, { "gene_id": 15043, "description": "histocompatibility 2, T region locus 3", "gene_symbol": "[\"H2-T3\"]", "do": null }, { "gene_id": 15064, "description": "major histocompatibility complex, class I-related", "gene_symbol": "[\"Mr1\"]", "do": null }, { "gene_id": 15114, "description": "huntingtin-associated protein 1", "gene_symbol": "[\"Hap1\"]", "do": null }, { "gene_id": 15116, "description": "hyaluronan synthase 1", "gene_symbol": "[\"Has1\"]", "do": null }, { "gene_id": 15117, "description": "hyaluronan synthase 2", "gene_symbol": "[\"Has2\"]", "do": null }, { "gene_id": 15118, "description": "hyaluronan synthase 3", "gene_symbol": "[\"Has3\"]", "do": null }, { "gene_id": 15139, "description": "hemolytic complement", "gene_symbol": "[\"Hc\"]", "do": null }, { "gene_id": 15159, "description": "holocytochrome c synthetase", "gene_symbol": "[\"Hccs\"]", "do": "[{\"label\":\"microphthalmia\",\"id\":\"DOID:10629\"}]" }, { "gene_id": 15160, "description": "serine (or cysteine) peptidase inhibitor, clade D, member 1", "gene_symbol": "[\"Serpind1\"]", "do": null }, { "gene_id": 15161, "description": "host cell factor C1", "gene_symbol": "[\"Hcfc1\"]", "do": "[{\"label\":\"methylmalonic acidemia and homocysteinemia cblX type\",\"id\":\"DOID:0111814\"}]" }, { "gene_id": 15165, "description": "hyperpolarization activated cyclic nucleotide gated potassium channel 1", "gene_symbol": "[\"Hcn1\"]", "do": "[{\"label\":\"sick sinus syndrome\",\"id\":\"DOID:13884\"}]" }, { "gene_id": 15166, "description": "hyperpolarization-activated, cyclic nucleotide-gated K+ 2", "gene_symbol": "[\"Hcn2\"]", "do": null }, { "gene_id": 15168, "description": "hyperpolarization-activated, cyclic nucleotide-gated K+ 3", "gene_symbol": "[\"Hcn3\"]", "do": null }, { "gene_id": 15170, "description": "protein tyrosine phosphatase, non-receptor type 6", "gene_symbol": "[\"Ptpn6\"]", "do": null }, { "gene_id": 15185, "description": "histone deacetylase 6", "gene_symbol": "[\"Hdac6\"]", "do": null }, { "gene_id": 15199, "description": "heme binding protein 1", "gene_symbol": "[\"Hebp1\"]", "do": null }, { "gene_id": 15200, "description": "heparin-binding EGF-like growth factor", "gene_symbol": "[\"Hbegf\"]", "do": null }, { "gene_id": 15203, "description": "hephaestin", "gene_symbol": "[\"Heph\"]", "do": null }, { "gene_id": 15204, "description": "HECT and RLD domain containing E3 ubiquitin protein ligase 2", "gene_symbol": "[\"Herc2\"]", "do": null }, { "gene_id": 15211, "description": "hexosaminidase A", "gene_symbol": "[\"Hexa\"]", "do": "[{\"label\":\"Tay-Sachs disease\",\"id\":\"DOID:3320\"}]" }, { "gene_id": 15212, "description": "hexosaminidase B", "gene_symbol": "[\"Hexb\"]", "do": "[{\"label\":\"Sandhoff disease\",\"id\":\"DOID:3323\"}]" }, { "gene_id": 15216, "description": "homeostatic iron regulator", "gene_symbol": "[\"Hfe\"]", "do": "[{\"label\":\"hemochromatosis type 1\",\"id\":\"DOID:0111029\"}]" }, { "gene_id": 15221, "description": "forkhead box D3", "gene_symbol": "[\"Foxd3\"]", "do": null }, { "gene_id": 15228, "description": "forkhead box G1", "gene_symbol": "[\"Foxg1\"]", "do": null }, { "gene_id": 15234, "description": "hepatocyte growth factor", "gene_symbol": "[\"Hgf\"]", "do": "[{\"label\":\"autosomal recessive nonsyndromic deafness 39\",\"id\":\"DOID:0110497\"},{\"label\":\"breast cancer\",\"id\":\"DOID:1612\"}]" }, { "gene_id": 15235, "description": "macrophage stimulating 1 (hepatocyte growth factor-like)", "gene_symbol": "[\"Mst1\"]", "do": null }, { "gene_id": 15239, "description": "HGF-regulated tyrosine kinase substrate", "gene_symbol": "[\"Hgs\"]", "do": null }, { "gene_id": 15245, "description": "Hedgehog-interacting protein", "gene_symbol": "[\"Hhip\"]", "do": null }, { "gene_id": 15247, "description": "solute carrier family 71 member 1", "gene_symbol": "[\"Slc72a1\"]", "do": null }, { "gene_id": 15257, "description": "homeodomain interacting protein kinase 1", "gene_symbol": "[\"Hipk1\"]", "do": null }, { "gene_id": 15258, "description": "homeodomain interacting protein kinase 2", "gene_symbol": "[\"Hipk2\"]", "do": null }, { "gene_id": 15260, "description": "histone cell cycle regulator", "gene_symbol": "[\"Hira\"]", "do": null }, { "gene_id": 15273, "description": "human immunodeficiency virus type I enhancer binding protein 2", "gene_symbol": "[\"Hivep2\"]", "do": "[{\"label\":\"intellectual disability\",\"id\":\"DOID:1059\"},{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 15275, "description": "hexokinase 1", "gene_symbol": "[\"Hk1\"]", "do": null }, { "gene_id": 15277, "description": "hexokinase 2", "gene_symbol": "[\"Hk2\"]", "do": null }, { "gene_id": 15356, "description": "3-hydroxy-3-methylglutaryl-Coenzyme A lyase", "gene_symbol": "[\"Hmgcl\"]", "do": null }, { "gene_id": 15357, "description": "3-hydroxy-3-methylglutaryl-Coenzyme A reductase", "gene_symbol": "[\"Hmgcr\"]", "do": null }, { "gene_id": 15360, "description": "3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2", "gene_symbol": "[\"Hmgcs2\"]", "do": "[{\"label\":\"HMG-CoA synthase 2 deficiency\",\"id\":\"DOID:0081168\"}]" }, { "gene_id": 15366, "description": "hyaluronan mediated motility receptor (RHAMM)", "gene_symbol": "[\"Hmmr\"]", "do": null }, { "gene_id": 15369, "description": "heme oxygenase 2", "gene_symbol": "[\"Hmox2\"]", "do": null }, { "gene_id": 15374, "description": "Jupiter microtubule associated homolog 1", "gene_symbol": "[\"Jpt1\"]", "do": null }, { "gene_id": 15379, "description": "one cut domain, family member 1", "gene_symbol": "[\"Onecut1\"]", "do": null }, { "gene_id": 15381, "description": "heterogeneous nuclear ribonucleoprotein C", "gene_symbol": "[\"Hnrnpc\"]", "do": null }, { "gene_id": 15382, "description": "heterogeneous nuclear ribonucleoprotein A1", "gene_symbol": "[\"Hnrnpa1\"]", "do": null }, { "gene_id": 15387, "description": "heterogeneous nuclear ribonucleoprotein K", "gene_symbol": "[\"Hnrnpk\"]", "do": null }, { "gene_id": 15410, "description": "homeobox B3", "gene_symbol": "[\"Hoxb3\"]", "do": null }, { "gene_id": 15439, "description": "haptoglobin", "gene_symbol": "[\"Hp\"]", "do": null }, { "gene_id": 15442, "description": "heparanase", "gene_symbol": "[\"Hpse\"]", "do": null }, { "gene_id": 15450, "description": "lipase C, hepatic type", "gene_symbol": "[\"Lipc\"]", "do": null }, { "gene_id": 15451, "description": "hepsin", "gene_symbol": "[\"Hpn\"]", "do": null }, { "gene_id": 15452, "description": "hypoxanthine phosphoribosyltransferase 1", "gene_symbol": "[\"Hprt1\"]", "do": "[{\"label\":\"Lesch-Nyhan syndrome\",\"id\":\"DOID:1919\"}]" }, { "gene_id": 15458, "description": "hemopexin", "gene_symbol": "[\"Hpx\"]", "do": null }, { "gene_id": 15463, "description": "ArfGAP with FG repeats 1", "gene_symbol": "[\"Agfg1\"]", "do": "[{\"label\":\"oligoasthenoteratozoospermia\",\"id\":\"DOID:0070311\"}]" }, { "gene_id": 15464, "description": "histidine rich calcium binding protein", "gene_symbol": "[\"Hrc\"]", "do": null }, { "gene_id": 15465, "description": "histamine receptor H1", "gene_symbol": "[\"Hrh1\"]", "do": null }, { "gene_id": 15466, "description": "histamine receptor H2", "gene_symbol": "[\"Hrh2\"]", "do": null }, { "gene_id": 15476, "description": "heparan sulfate (glucosamine) 3-O-sulfotransferase 1", "gene_symbol": "[\"Hs3st1\"]", "do": null }, { "gene_id": 15478, "description": "heparan sulfate (glucosamine) 3-O-sulfotransferase 3A1", "gene_symbol": "[\"Hs3st3a1\"]", "do": null }, { "gene_id": 15481, "description": "heat shock protein family A (Hsp70) member 8", "gene_symbol": "[\"Hspa8\"]", "do": null }, { "gene_id": 15482, "description": "heat shock protein 1-like", "gene_symbol": "[\"Hspa1l\"]", "do": null }, { "gene_id": 15483, "description": "hydroxysteroid 11-beta dehydrogenase 1", "gene_symbol": "[\"Hsd11b1\"]", "do": "[{\"label\":\"cortisone reductase deficiency 2\",\"id\":\"DOID:0090140\"}]" }, { "gene_id": 15486, "description": "hydroxysteroid (17-beta) dehydrogenase 2", "gene_symbol": "[\"Hsd17b2\"]", "do": null }, { "gene_id": 15488, "description": "hydroxysteroid (17-beta) dehydrogenase 4", "gene_symbol": "[\"Hsd17b4\"]", "do": "[{\"label\":\"D-bifunctional protein deficiency\",\"id\":\"DOID:0090031\"}]" }, { "gene_id": 15490, "description": "hydroxysteroid (17-beta) dehydrogenase 7", "gene_symbol": "[\"Hsd17b7\"]", "do": null }, { "gene_id": 15499, "description": "heat shock factor 1", "gene_symbol": "[\"Hsf1\"]", "do": null }, { "gene_id": 15502, "description": "DnaJ heat shock protein family (Hsp40) member A1", "gene_symbol": "[\"Dnaja1\"]", "do": null }, { "gene_id": 15505, "description": "heat shock 105kDa/110kDa protein 1", "gene_symbol": "[\"Hsph1\"]", "do": null }, { "gene_id": 15507, "description": "heat shock protein family B (small) member 1", "gene_symbol": "[\"Hspb1\"]", "do": null }, { "gene_id": 15510, "description": "heat shock protein 1 (chaperonin)", "gene_symbol": "[\"Hspd1\"]", "do": "[{\"label\":\"hereditary spastic paraplegia 13\",\"id\":\"DOID:0110766\"}]" }, { "gene_id": 15516, "description": "heat shock protein 90 alpha (cytosolic), class B member 1", "gene_symbol": "[\"Hsp90ab1\"]", "do": null }, { "gene_id": 15519, "description": "heat shock protein 90, alpha (cytosolic), class A member 1", "gene_symbol": "[\"Hsp90aa1\"]", "do": null }, { "gene_id": 15526, "description": "heat shock protein family A (Hsp70) member 9", "gene_symbol": "[\"Hspa9\"]", "do": null }, { "gene_id": 15529, "description": "syndecan 2", "gene_symbol": "[\"Sdc2\"]", "do": null }, { "gene_id": 15530, "description": "perlecan (heparan sulfate proteoglycan 2)", "gene_symbol": "[\"Hspg2\"]", "do": "[{\"label\":\"Schwartz-Jampel syndrome 1\",\"id\":\"DOID:0090005\"},{\"label\":\"Silverman-Handmaker type dyssegmental dysplasia\",\"id\":\"DOID:0090032\"},{\"label\":\"dextro-looped transposition of the great arteries\",\"id\":\"DOID:0060770\"},{\"label\":\"thanatophoric dysplasia\",\"id\":\"DOID:13481\"}]" }, { "gene_id": 15531, "description": "N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1", "gene_symbol": "[\"Ndst1\"]", "do": "[{\"label\":\"DiGeorge syndrome\",\"id\":\"DOID:11198\"},{\"label\":\"congenital diaphragmatic hernia\",\"id\":\"DOID:3827\"},{\"label\":\"newborn respiratory distress syndrome\",\"id\":\"DOID:12716\"}]" }, { "gene_id": 15550, "description": "5-hydroxytryptamine (serotonin) receptor 1A", "gene_symbol": "[\"Htr1a\"]", "do": "[{\"label\":\"anxiety disorder\",\"id\":\"DOID:2030\"}]" }, { "gene_id": 15551, "description": "5-hydroxytryptamine (serotonin) receptor 1B", "gene_symbol": "[\"Htr1b\"]", "do": null }, { "gene_id": 15552, "description": "5-hydroxytryptamine (serotonin) receptor 1D", "gene_symbol": "[\"Htr1d\"]", "do": null }, { "gene_id": 15557, "description": "5-hydroxytryptamine (serotonin) receptor 1F", "gene_symbol": "[\"Htr1f\"]", "do": null }, { "gene_id": 15558, "description": "5-hydroxytryptamine (serotonin) receptor 2A", "gene_symbol": "[\"Htr2a\"]", "do": null }, { "gene_id": 15559, "description": "5-hydroxytryptamine (serotonin) receptor 2B", "gene_symbol": "[\"Htr2b\"]", "do": "[{\"label\":\"hypertrophic cardiomyopathy\",\"id\":\"DOID:11984\"}]" }, { "gene_id": 15560, "description": "5-hydroxytryptamine (serotonin) receptor 2C", "gene_symbol": "[\"Htr2c\"]", "do": "[{\"label\":\"Prader-Willi syndrome\",\"id\":\"DOID:11983\"},{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 15561, "description": "5-hydroxytryptamine (serotonin) receptor 3A", "gene_symbol": "[\"Htr3a\"]", "do": null }, { "gene_id": 15562, "description": "5 hydroxytryptamine (serotonin) receptor 4", "gene_symbol": "[\"Htr4\"]", "do": "[{\"label\":\"anorexia nervosa\",\"id\":\"DOID:8689\"}]" }, { "gene_id": 15563, "description": "5-hydroxytryptamine (serotonin) receptor 5A", "gene_symbol": "[\"Htr5a\"]", "do": null }, { "gene_id": 15565, "description": "5-hydroxytryptamine (serotonin) receptor 6", "gene_symbol": "[\"Htr6\"]", "do": null }, { "gene_id": 15566, "description": "5-hydroxytryptamine (serotonin) receptor 7", "gene_symbol": "[\"Htr7\"]", "do": null }, { "gene_id": 15567, "description": "solute carrier family 6 (neurotransmitter transporter, serotonin), member 4", "gene_symbol": "[\"Slc6a4\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"sudden infant death syndrome\",\"id\":\"DOID:9007\"}]" }, { "gene_id": 15586, "description": "hyaluronoglucosaminidase 1", "gene_symbol": "[\"Hyal1\"]", "do": "[{\"label\":\"mucopolysaccharidosis IX\",\"id\":\"DOID:0050809\"}]" }, { "gene_id": 15587, "description": "hyaluronoglucosaminidase 2", "gene_symbol": "[\"Hyal2\"]", "do": null }, { "gene_id": 15891, "description": "integrin binding sialoprotein", "gene_symbol": "[\"Ibsp\"]", "do": null }, { "gene_id": 15894, "description": "intercellular adhesion molecule 1", "gene_symbol": "[\"Icam1\"]", "do": "[{\"label\":\"malaria\",\"id\":\"DOID:12365\"}]" }, { "gene_id": 15896, "description": "intercellular adhesion molecule 2", "gene_symbol": "[\"Icam2\"]", "do": null }, { "gene_id": 15898, "description": "intercellular adhesion molecule 5, telencephalin", "gene_symbol": "[\"Icam5\"]", "do": null }, { "gene_id": 15926, "description": "isocitrate dehydrogenase 1 (NADP+), soluble", "gene_symbol": "[\"Idh1\"]", "do": null }, { "gene_id": 15931, "description": "iduronate 2-sulfatase", "gene_symbol": "[\"Ids\"]", "do": "[{\"label\":\"mucopolysaccharidosis II\",\"id\":\"DOID:12799\"}]" }, { "gene_id": 15932, "description": "iduronidase, alpha-L", "gene_symbol": "[\"Idua\"]", "do": "[{\"label\":\"mucopolysaccharidosis I\",\"id\":\"DOID:12802\"},{\"label\":\"otitis media\",\"id\":\"DOID:10754\"}]" }, { "gene_id": 15937, "description": "immediate early response 3", "gene_symbol": "[\"Ier3\"]", "do": null }, { "gene_id": 15962, "description": "interferon alpha 1", "gene_symbol": "[\"Ifna1\"]", "do": null }, { "gene_id": 15964, "description": "interferon alpha 11", "gene_symbol": "[\"Ifna11\"]", "do": null }, { "gene_id": 15967, "description": "interferon alpha 4", "gene_symbol": "[\"Ifna4\"]", "do": null }, { "gene_id": 15972, "description": "interferon alpha 9", "gene_symbol": "[\"Ifna9\"]", "do": null }, { "gene_id": 15975, "description": "interferon (alpha and beta) receptor 1", "gene_symbol": "[\"Ifnar1\"]", "do": null }, { "gene_id": 15976, "description": "interferon (alpha and beta) receptor 2", "gene_symbol": "[\"Ifnar2\"]", "do": null }, { "gene_id": 15977, "description": "interferon beta 1, fibroblast", "gene_symbol": "[\"Ifnb1\"]", "do": null }, { "gene_id": 15978, "description": "interferon gamma", "gene_symbol": "[\"Ifng\"]", "do": "[{\"label\":\"aplastic anemia\",\"id\":\"DOID:12449\"},{\"label\":\"cardiomyopathy\",\"id\":\"DOID:0050700\"},{\"label\":\"hepatitis\",\"id\":\"DOID:2237\"},{\"label\":\"malaria\",\"id\":\"DOID:12365\"},{\"label\":\"medulloblastoma\",\"id\":\"DOID:0050902\"},{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 15979, "description": "interferon gamma receptor 1", "gene_symbol": "[\"Ifngr1\"]", "do": "[{\"label\":\"osteoporosis\",\"id\":\"DOID:11476\"}]" }, { "gene_id": 15980, "description": "interferon gamma receptor 2", "gene_symbol": "[\"Ifngr2\"]", "do": "[{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 15985, "description": "CD79B antigen", "gene_symbol": "[\"Cd79b\"]", "do": null }, { "gene_id": 16001, "description": "insulin-like growth factor I receptor", "gene_symbol": "[\"Igf1r\"]", "do": null }, { "gene_id": 16002, "description": "insulin-like growth factor 2", "gene_symbol": "[\"Igf2\"]", "do": "[{\"label\":\"type 1 diabetes mellitus 2\",\"id\":\"DOID:0110741\"}]" }, { "gene_id": 16004, "description": "insulin-like growth factor 2 receptor", "gene_symbol": "[\"Igf2r\"]", "do": null }, { "gene_id": 16005, "description": "insulin-like growth factor binding protein, acid labile subunit", "gene_symbol": "[\"Igfals\"]", "do": null }, { "gene_id": 16009, "description": "insulin-like growth factor binding protein 3", "gene_symbol": "[\"Igfbp3\"]", "do": null }, { "gene_id": 16010, "description": "insulin-like growth factor binding protein 4", "gene_symbol": "[\"Igfbp4\"]", "do": null }, { "gene_id": 16068, "description": "interleukin 18 binding protein", "gene_symbol": "[\"Il18bp\"]", "do": null }, { "gene_id": 16069, "description": "immunoglobulin joining chain", "gene_symbol": "[\"Jchain\"]", "do": null }, { "gene_id": 16147, "description": "Indian hedgehog", "gene_symbol": "[\"Ihh\"]", "do": "[{\"label\":\"Hirschsprung's disease\",\"id\":\"DOID:10487\"},{\"label\":\"annular pancreas\",\"id\":\"DOID:0060850\"},{\"label\":\"brachydactyly type A1\",\"id\":\"DOID:0110964\"}]" }, { "gene_id": 16149, "description": "CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)", "gene_symbol": "[\"Cd74\"]", "do": null }, { "gene_id": 16150, "description": "inhibitor of kappaB kinase beta", "gene_symbol": "[\"Ikbkb\"]", "do": "[{\"label\":\"immunodeficiency 15A\",\"id\":\"DOID:0111960\"}]" }, { "gene_id": 16153, "description": "interleukin 10", "gene_symbol": "[\"Il10\"]", "do": "[{\"label\":\"inflammatory bowel disease\",\"id\":\"DOID:0050589\"}]" }, { "gene_id": 16154, "description": "interleukin 10 receptor, alpha", "gene_symbol": "[\"Il10ra\"]", "do": null }, { "gene_id": 16155, "description": "interleukin 10 receptor, beta", "gene_symbol": "[\"Il10rb\"]", "do": null }, { "gene_id": 16157, "description": "interleukin 11 receptor subunit alpha 1", "gene_symbol": "[\"Il11ra1\"]", "do": null }, { "gene_id": 16158, "description": "interleukin 11 receptor subunit alpha 2", "gene_symbol": "[\"Il11ra2\"]", "do": null }, { "gene_id": 16159, "description": "interleukin 12a", "gene_symbol": "[\"Il12a\"]", "do": null }, { "gene_id": 16160, "description": "interleukin 12b", "gene_symbol": "[\"Il12b\"]", "do": null }, { "gene_id": 16161, "description": "interleukin 12 receptor, beta 1", "gene_symbol": "[\"Il12rb1\"]", "do": null }, { "gene_id": 16162, "description": "interleukin 12 receptor, beta 2", "gene_symbol": "[\"Il12rb2\"]", "do": null }, { "gene_id": 16163, "description": "interleukin 13", "gene_symbol": "[\"Il13\"]", "do": "[{\"label\":\"atopic dermatitis\",\"id\":\"DOID:3310\"}]" }, { "gene_id": 16164, "description": "interleukin 13 receptor, alpha 1", "gene_symbol": "[\"Il13ra1\"]", "do": null }, { "gene_id": 16165, "description": "interleukin 13 receptor, alpha 2", "gene_symbol": "[\"Il13ra2\"]", "do": null }, { "gene_id": 16168, "description": "interleukin 15", "gene_symbol": "[\"Il15\"]", "do": null }, { "gene_id": 16169, "description": "interleukin 15 receptor, alpha chain", "gene_symbol": "[\"Il15ra\"]", "do": null }, { "gene_id": 16170, "description": "interleukin 16", "gene_symbol": "[\"Il16\"]", "do": null }, { "gene_id": 16171, "description": "interleukin 17A", "gene_symbol": "[\"Il17a\"]", "do": null }, { "gene_id": 16172, "description": "interleukin 17 receptor A", "gene_symbol": "[\"Il17ra\"]", "do": null }, { "gene_id": 16174, "description": "interleukin 18 receptor accessory protein", "gene_symbol": "[\"Il18rap\"]", "do": null }, { "gene_id": 16175, "description": "interleukin 1 alpha", "gene_symbol": "[\"Il1a\"]", "do": null }, { "gene_id": 16177, "description": "interleukin 1 receptor, type I", "gene_symbol": "[\"Il1r1\"]", "do": "[{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 16178, "description": "interleukin 1 receptor, type II", "gene_symbol": "[\"Il1r2\"]", "do": null }, { "gene_id": 16180, "description": "interleukin 1 receptor accessory protein", "gene_symbol": "[\"Il1rap\"]", "do": null }, { "gene_id": 16181, "description": "interleukin 1 receptor antagonist", "gene_symbol": "[\"Il1rn\"]", "do": null }, { "gene_id": 16182, "description": "interleukin 18 receptor 1", "gene_symbol": "[\"Il18r1\"]", "do": null }, { "gene_id": 16183, "description": "interleukin 2", "gene_symbol": "[\"Il2\"]", "do": "[{\"label\":\"Sjogren's syndrome\",\"id\":\"DOID:12894\"},{\"label\":\"inflammatory bowel disease\",\"id\":\"DOID:0050589\"}]" }, { "gene_id": 16184, "description": "interleukin 2 receptor, alpha chain", "gene_symbol": "[\"Il2ra\"]", "do": "[{\"label\":\"Sjogren's syndrome\",\"id\":\"DOID:12894\"},{\"label\":\"inflammatory bowel disease\",\"id\":\"DOID:0050589\"}]" }, { "gene_id": 16185, "description": "interleukin 2 receptor, beta chain", "gene_symbol": "[\"Il2rb\"]", "do": null }, { "gene_id": 16186, "description": "interleukin 2 receptor, gamma chain", "gene_symbol": "[\"Il2rg\"]", "do": null }, { "gene_id": 16187, "description": "interleukin 3", "gene_symbol": "[\"Il3\"]", "do": null }, { "gene_id": 16188, "description": "interleukin 3 receptor, alpha chain", "gene_symbol": "[\"Il3ra\"]", "do": null }, { "gene_id": 16189, "description": "interleukin 4", "gene_symbol": "[\"Il4\"]", "do": "[{\"label\":\"Sjogren's syndrome\",\"id\":\"DOID:12894\"},{\"label\":\"atopic dermatitis\",\"id\":\"DOID:3310\"},{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 16190, "description": "interleukin 4 receptor, alpha", "gene_symbol": "[\"Il4ra\"]", "do": "[{\"label\":\"asthma\",\"id\":\"DOID:2841\"}]" }, { "gene_id": 16191, "description": "interleukin 5", "gene_symbol": "[\"Il5\"]", "do": null }, { "gene_id": 16192, "description": "interleukin 5 receptor, alpha", "gene_symbol": "[\"Il5ra\"]", "do": null }, { "gene_id": 16194, "description": "interleukin 6 receptor, alpha", "gene_symbol": "[\"Il6ra\"]", "do": null }, { "gene_id": 16195, "description": "interleukin 6 signal transducer", "gene_symbol": "[\"Il6st\"]", "do": "[{\"label\":\"rheumatoid arthritis\",\"id\":\"DOID:7148\"},{\"label\":\"stomach cancer\",\"id\":\"DOID:10534\"}]" }, { "gene_id": 16196, "description": "interleukin 7", "gene_symbol": "[\"Il7\"]", "do": null }, { "gene_id": 16197, "description": "interleukin 7 receptor", "gene_symbol": "[\"Il7r\"]", "do": null }, { "gene_id": 16198, "description": "interleukin 9", "gene_symbol": "[\"Il9\"]", "do": null }, { "gene_id": 16199, "description": "interleukin 9 receptor", "gene_symbol": "[\"Il9r\"]", "do": null }, { "gene_id": 16206, "description": "leucine-rich repeats and immunoglobulin-like domains 1", "gene_symbol": "[\"Lrig1\"]", "do": null }, { "gene_id": 16319, "description": "inner centromere protein", "gene_symbol": "[\"Incenp\"]", "do": null }, { "gene_id": 16322, "description": "inhibin alpha", "gene_symbol": "[\"Inha\"]", "do": null }, { "gene_id": 16323, "description": "inhibin beta-A", "gene_symbol": "[\"Inhba\"]", "do": null }, { "gene_id": 16324, "description": "inhibin beta-B", "gene_symbol": "[\"Inhbb\"]", "do": null }, { "gene_id": 16325, "description": "inhibin beta-C", "gene_symbol": "[\"Inhbc\"]", "do": null }, { "gene_id": 16326, "description": "inhibin beta-E", "gene_symbol": "[\"Inhbe\"]", "do": null }, { "gene_id": 16329, "description": "inositol polyphosphate-1-phosphatase", "gene_symbol": "[\"Inpp1\"]", "do": null }, { "gene_id": 16332, "description": "inositol polyphosphate phosphatase-like 1", "gene_symbol": "[\"Inppl1\"]", "do": null }, { "gene_id": 16333, "description": "insulin I", "gene_symbol": "[\"Ins1\"]", "do": null }, { "gene_id": 16334, "description": "insulin II", "gene_symbol": "[\"Ins2\"]", "do": "[{\"label\":\"maturity-onset diabetes of the young\",\"id\":\"DOID:0050524\"},{\"label\":\"neonatal diabetes mellitus\",\"id\":\"DOID:11717\"},{\"label\":\"permanent neonatal diabetes mellitus\",\"id\":\"DOID:0060639\"},{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"},{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 16337, "description": "insulin receptor", "gene_symbol": "[\"Insr\"]", "do": "[{\"label\":\"diabetic retinopathy\",\"id\":\"DOID:8947\"}]" }, { "gene_id": 16367, "description": "insulin receptor substrate 1", "gene_symbol": "[\"Irs1\"]", "do": "[{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 16398, "description": "integrin alpha 2", "gene_symbol": "[\"Itga2\"]", "do": null }, { "gene_id": 16399, "description": "integrin alpha 2b", "gene_symbol": "[\"Itga2b\"]", "do": "[{\"label\":\"platelet-type bleeding disorder 16\",\"id\":\"DOID:0060691\"}]" }, { "gene_id": 16400, "description": "integrin alpha 3", "gene_symbol": "[\"Itga3\"]", "do": null }, { "gene_id": 16401, "description": "integrin alpha 4", "gene_symbol": "[\"Itga4\"]", "do": null }, { "gene_id": 16402, "description": "integrin alpha 5 (fibronectin receptor alpha)", "gene_symbol": "[\"Itga5\"]", "do": null }, { "gene_id": 16403, "description": "integrin alpha 6", "gene_symbol": "[\"Itga6\"]", "do": "[{\"label\":\"junctional epidermolysis bullosa Herlitz type\",\"id\":\"DOID:0060737\"}]" }, { "gene_id": 16404, "description": "integrin alpha 7", "gene_symbol": "[\"Itga7\"]", "do": "[{\"label\":\"congenital muscular dystrophy due to integrin alpha-7 deficiency\",\"id\":\"DOID:0110639\"}]" }, { "gene_id": 16407, "description": "integrin alpha E, epithelial-associated", "gene_symbol": "[\"Itgae\"]", "do": null }, { "gene_id": 16408, "description": "integrin alpha L", "gene_symbol": "[\"Itgal\"]", "do": null }, { "gene_id": 16409, "description": "integrin alpha M", "gene_symbol": "[\"Itgam\"]", "do": null }, { "gene_id": 16410, "description": "integrin alpha V", "gene_symbol": "[\"Itgav\"]", "do": null }, { "gene_id": 16411, "description": "integrin alpha X", "gene_symbol": "[\"Itgax\"]", "do": null }, { "gene_id": 16412, "description": "integrin beta 1 (fibronectin receptor beta)", "gene_symbol": "[\"Itgb1\"]", "do": "[{\"label\":\"Hirschsprung's disease\",\"id\":\"DOID:10487\"}]" }, { "gene_id": 16414, "description": "integrin beta 2", "gene_symbol": "[\"Itgb2\"]", "do": "[{\"label\":\"leukocyte adhesion deficiency 1\",\"id\":\"DOID:0110910\"},{\"label\":\"psoriasis\",\"id\":\"DOID:8893\"}]" }, { "gene_id": 16415, "description": "integrin beta 2-like", "gene_symbol": "[\"Itgb2l\"]", "do": null }, { "gene_id": 16416, "description": "integrin beta 3", "gene_symbol": "[\"Itgb3\"]", "do": "[{\"label\":\"Glanzmann's thrombasthenia\",\"id\":\"DOID:2219\"},{\"label\":\"platelet-type bleeding disorder 16\",\"id\":\"DOID:0060691\"}]" }, { "gene_id": 16418, "description": "eukaryotic translation initiation factor 6", "gene_symbol": "[\"Eif6\"]", "do": null }, { "gene_id": 16419, "description": "integrin beta 5", "gene_symbol": "[\"Itgb5\"]", "do": null }, { "gene_id": 16420, "description": "integrin beta 6", "gene_symbol": "[\"Itgb6\"]", "do": "[{\"label\":\"asthma\",\"id\":\"DOID:2841\"},{\"label\":\"pulmonary emphysema\",\"id\":\"DOID:9675\"}]" }, { "gene_id": 16421, "description": "integrin beta 7", "gene_symbol": "[\"Itgb7\"]", "do": null }, { "gene_id": 16423, "description": "CD47 antigen (Rh-related antigen, integrin-associated signal transducer)", "gene_symbol": "[\"Cd47\"]", "do": null }, { "gene_id": 16424, "description": "inter-alpha trypsin inhibitor, heavy chain 1", "gene_symbol": "[\"Itih1\"]", "do": null }, { "gene_id": 16425, "description": "inter-alpha trypsin inhibitor, heavy chain 2", "gene_symbol": "[\"Itih2\"]", "do": null }, { "gene_id": 16426, "description": "inter-alpha trypsin inhibitor, heavy chain 3", "gene_symbol": "[\"Itih3\"]", "do": null }, { "gene_id": 16427, "description": "inter alpha-trypsin inhibitor, heavy chain 4", "gene_symbol": "[\"Itih4\"]", "do": null }, { "gene_id": 16430, "description": "STT3, subunit of the oligosaccharyltransferase complex, homolog A (S. cerevisiae)", "gene_symbol": "[\"Stt3a\"]", "do": null }, { "gene_id": 16431, "description": "integral membrane protein 2A", "gene_symbol": "[\"Itm2a\"]", "do": null }, { "gene_id": 16432, "description": "integral membrane protein 2B", "gene_symbol": "[\"Itm2b\"]", "do": "[{\"label\":\"cerebral amyloid angiopathy\",\"id\":\"DOID:9246\"}]" }, { "gene_id": 16433, "description": "CUB and zona pellucida-like domains 1", "gene_symbol": "[\"Cuzd1\"]", "do": null }, { "gene_id": 16438, "description": "inositol 1,4,5-trisphosphate receptor 1", "gene_symbol": "[\"Itpr1\"]", "do": null }, { "gene_id": 16440, "description": "inositol 1,4,5-triphosphate receptor 3", "gene_symbol": "[\"Itpr3\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 16443, "description": "intersectin 1 (SH3 domain protein 1A)", "gene_symbol": "[\"Itsn1\"]", "do": null }, { "gene_id": 16449, "description": "jagged 1", "gene_symbol": "[\"Jag1\"]", "do": "[{\"label\":\"Alagille syndrome\",\"id\":\"DOID:9245\"}]" }, { "gene_id": 16450, "description": "jagged 2", "gene_symbol": "[\"Jag2\"]", "do": null }, { "gene_id": 16456, "description": "F11 receptor", "gene_symbol": "[\"F11r\"]", "do": null }, { "gene_id": 16475, "description": "ajuba LIM protein", "gene_symbol": "[\"Ajuba\"]", "do": null }, { "gene_id": 16476, "description": "Jun proto-oncogene, AP-1 transcription factor subunit", "gene_symbol": "[\"Jun\"]", "do": "[{\"label\":\"pulmonary emphysema\",\"id\":\"DOID:9675\"}]" }, { "gene_id": 16478, "description": "jun D proto-oncogene, AP-1 transcription factor subunit", "gene_symbol": "[\"Jund\"]", "do": null }, { "gene_id": 16480, "description": "junction plakoglobin", "gene_symbol": "[\"Jup\"]", "do": "[{\"label\":\"arrhythmogenic right ventricular dysplasia 12\",\"id\":\"DOID:0110083\"},{\"label\":\"epidermolytic hyperkeratosis\",\"id\":\"DOID:4603\"}]" }, { "gene_id": 16485, "description": "potassium voltage-gated channel, shaker-related subfamily, member 1", "gene_symbol": "[\"Kcna1\"]", "do": "[{\"label\":\"epilepsy\",\"id\":\"DOID:1826\"},{\"label\":\"episodic ataxia type 1\",\"id\":\"DOID:0050989\"},{\"label\":\"temporal lobe epilepsy\",\"id\":\"DOID:3328\"}]" }, { "gene_id": 16490, "description": "potassium voltage-gated channel, shaker-related subfamily, member 2", "gene_symbol": "[\"Kcna2\"]", "do": null }, { "gene_id": 16491, "description": "potassium voltage-gated channel, shaker-related subfamily, member 3", "gene_symbol": "[\"Kcna3\"]", "do": null }, { "gene_id": 16492, "description": "potassium voltage-gated channel, shaker-related subfamily, member 4", "gene_symbol": "[\"Kcna4\"]", "do": null }, { "gene_id": 16493, "description": "potassium voltage-gated channel, shaker-related subfamily, member 5", "gene_symbol": "[\"Kcna5\"]", "do": null }, { "gene_id": 16495, "description": "potassium voltage-gated channel, shaker-related subfamily, member 7", "gene_symbol": "[\"Kcna7\"]", "do": null }, { "gene_id": 16498, "description": "potassium voltage-gated channel, shaker-related subfamily, beta member 2", "gene_symbol": "[\"Kcnab2\"]", "do": "[{\"label\":\"chromosome 1p36 deletion syndrome\",\"id\":\"DOID:0060410\"}]" }, { "gene_id": 16500, "description": "potassium voltage gated channel, Shab-related subfamily, member 1", "gene_symbol": "[\"Kcnb1\"]", "do": null }, { "gene_id": 16502, "description": "potassium voltage gated channel, Shaw-related subfamily, member 1", "gene_symbol": "[\"Kcnc1\"]", "do": null }, { "gene_id": 16504, "description": "potassium voltage gated channel, Shaw-related subfamily, member 3", "gene_symbol": "[\"Kcnc3\"]", "do": null }, { "gene_id": 16506, "description": "potassium voltage-gated channel, Shal-related family, member 1", "gene_symbol": "[\"Kcnd1\"]", "do": null }, { "gene_id": 16508, "description": "potassium voltage-gated channel, Shal-related family, member 2", "gene_symbol": "[\"Kcnd2\"]", "do": null }, { "gene_id": 16509, "description": "potassium voltage-gated channel, Isk-related subfamily, member 1", "gene_symbol": "[\"Kcne1\"]", "do": "[{\"label\":\"Jervell-Lange Nielsen syndrome\",\"id\":\"DOID:2842\"}]" }, { "gene_id": 16510, "description": "potassium voltage-gated channel, subfamily H (eag-related), member 1", "gene_symbol": "[\"Kcnh1\"]", "do": null }, { "gene_id": 16511, "description": "potassium voltage-gated channel, subfamily H (eag-related), member 2", "gene_symbol": "[\"Kcnh2\"]", "do": "[{\"label\":\"short QT syndrome\",\"id\":\"DOID:0050793\"}]" }, { "gene_id": 16512, "description": "potassium voltage-gated channel, subfamily H (eag-related), member 3", "gene_symbol": "[\"Kcnh3\"]", "do": null }, { "gene_id": 16514, "description": "potassium inwardly rectifying channel, subfamily J, member 11", "gene_symbol": "[\"Kcnj11\"]", "do": "[{\"label\":\"permanent neonatal diabetes mellitus\",\"id\":\"DOID:0060639\"}]" }, { "gene_id": 16519, "description": "potassium inwardly-rectifying channel, subfamily J, member 3", "gene_symbol": "[\"Kcnj3\"]", "do": null }, { "gene_id": 16525, "description": "potassium channel, subfamily K, member 1", "gene_symbol": "[\"Kcnk1\"]", "do": null }, { "gene_id": 16526, "description": "potassium channel, subfamily K, member 2", "gene_symbol": "[\"Kcnk2\"]", "do": null }, { "gene_id": 16527, "description": "potassium channel, subfamily K, member 3", "gene_symbol": "[\"Kcnk3\"]", "do": null }, { "gene_id": 16528, "description": "potassium channel, subfamily K, member 4", "gene_symbol": "[\"Kcnk4\"]", "do": null }, { "gene_id": 16530, "description": "potassium channel, subfamily K, member 7", "gene_symbol": "[\"Kcnk7\"]", "do": null }, { "gene_id": 16531, "description": "potassium large conductance calcium-activated channel, subfamily M, alpha member 1", "gene_symbol": "[\"Kcnma1\"]", "do": null }, { "gene_id": 16533, "description": "potassium large conductance calcium-activated channel, subfamily M, beta member 1", "gene_symbol": "[\"Kcnmb1\"]", "do": null }, { "gene_id": 16535, "description": "potassium voltage-gated channel, subfamily Q, member 1", "gene_symbol": "[\"Kcnq1\"]", "do": "[{\"label\":\"Jervell-Lange Nielsen syndrome\",\"id\":\"DOID:2842\"},{\"label\":\"long QT syndrome 1\",\"id\":\"DOID:0110644\"}]" }, { "gene_id": 16536, "description": "potassium voltage-gated channel, subfamily Q, member 2", "gene_symbol": "[\"Kcnq2\"]", "do": "[{\"label\":\"benign neonatal seizures\",\"id\":\"DOID:14264\"},{\"label\":\"developmental and epileptic encephalopathy 7\",\"id\":\"DOID:0080462\"}]" }, { "gene_id": 16541, "description": "napsin A aspartic peptidase", "gene_symbol": "[\"Napsa\"]", "do": null }, { "gene_id": 16542, "description": "kinase insert domain protein receptor", "gene_symbol": "[\"Kdr\"]", "do": null }, { "gene_id": 16545, "description": "keratocan", "gene_symbol": "[\"Kera\"]", "do": "[{\"label\":\"cornea plana\",\"id\":\"DOID:0060287\"}]" }, { "gene_id": 16548, "description": "ketohexokinase", "gene_symbol": "[\"Khk\"]", "do": null }, { "gene_id": 16549, "description": "KH-type splicing regulatory protein", "gene_symbol": "[\"Khsrp\"]", "do": null }, { "gene_id": 16554, "description": "kinesin family member 13B", "gene_symbol": "[\"Kif13b\"]", "do": null }, { "gene_id": 16558, "description": "kinesin family member 16B", "gene_symbol": "[\"Kif16b\"]", "do": null }, { "gene_id": 16562, "description": "kinesin family member 1C", "gene_symbol": "[\"Kif1c\"]", "do": null }, { "gene_id": 16563, "description": "kinesin family member 2A", "gene_symbol": "[\"Kif2a\"]", "do": null }, { "gene_id": 16564, "description": "kinesin family member 21A", "gene_symbol": "[\"Kif21a\"]", "do": "[{\"label\":\"congenital fibrosis of the extraocular muscles\",\"id\":\"DOID:0080143\"}]" }, { "gene_id": 16565, "description": "kinesin family member 21B", "gene_symbol": "[\"Kif21b\"]", "do": null }, { "gene_id": 16568, "description": "kinesin family member 3A", "gene_symbol": "[\"Kif3a\"]", "do": "[{\"label\":\"dysostosis\",\"id\":\"DOID:1934\"},{\"label\":\"polycystic kidney disease\",\"id\":\"DOID:0080322\"}]" }, { "gene_id": 16569, "description": "kinesin family member 3B", "gene_symbol": "[\"Kif3b\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 16571, "description": "kinesin family member 4", "gene_symbol": "[\"Kif4\"]", "do": null }, { "gene_id": 16573, "description": "kinesin family member 5B", "gene_symbol": "[\"Kif5b\"]", "do": null }, { "gene_id": 16590, "description": "Kit proto-oncogene receptor tyrosine kinase", "gene_symbol": "[\"Kit\"]", "do": "[{\"label\":\"gastrointestinal stromal tumor\",\"id\":\"DOID:9253\"},{\"label\":\"macrocytic anemia\",\"id\":\"DOID:2361\"},{\"label\":\"mastocytosis\",\"id\":\"DOID:350\"},{\"label\":\"piebaldism\",\"id\":\"DOID:3263\"}]" }, { "gene_id": 16591, "description": "klotho", "gene_symbol": "[\"Kl\"]", "do": "[{\"label\":\"hyperphosphatemic familial tumoral calcinosis\",\"id\":\"DOID:0111063\"},{\"label\":\"pulmonary emphysema\",\"id\":\"DOID:9675\"}]" }, { "gene_id": 16592, "description": "fatty acid binding protein 5, epidermal", "gene_symbol": "[\"Fabp5\"]", "do": null }, { "gene_id": 16599, "description": "Kruppel-like transcription factor 3 (basic)", "gene_symbol": "[\"Klf3\"]", "do": null }, { "gene_id": 16600, "description": "Kruppel-like transcription factor 4 (gut)", "gene_symbol": "[\"Klf4\"]", "do": null }, { "gene_id": 16612, "description": "kallikrein 1", "gene_symbol": "[\"Klk1\"]", "do": null }, { "gene_id": 16613, "description": "kallikrein 1-related peptidase b11", "gene_symbol": "[\"Klk1b11\"]", "do": null }, { "gene_id": 16615, "description": "kallikrein 1-related peptidase b16", "gene_symbol": "[\"Klk1b16\"]", "do": null }, { "gene_id": 16616, "description": "kallikrein 1-related peptidase b21", "gene_symbol": "[\"Klk1b21\"]", "do": null }, { "gene_id": 16617, "description": "kallikrein 1-related peptidase b24", "gene_symbol": "[\"Klk1b24\"]", "do": null }, { "gene_id": 16618, "description": "kallikrein 1-related petidase b26", "gene_symbol": "[\"Klk1b26\"]", "do": null }, { "gene_id": 16619, "description": "kallikrein 1-related peptidase b27", "gene_symbol": "[\"Klk1b27\"]", "do": null }, { "gene_id": 16621, "description": "kallikrein B, plasma 1", "gene_symbol": "[\"Klkb1\"]", "do": null }, { "gene_id": 16622, "description": "kallikrein 1-related peptidase b5", "gene_symbol": "[\"Klk1b5\"]", "do": null }, { "gene_id": 16623, "description": "kallikrein 1-related peptidase b1", "gene_symbol": "[\"Klk1b1\"]", "do": null }, { "gene_id": 16624, "description": "kallikrein 1-related peptidase b8", "gene_symbol": "[\"Klk1b8\"]", "do": null }, { "gene_id": 16625, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 3C", "gene_symbol": "[\"Serpina3c\"]", "do": null }, { "gene_id": 16633, "description": "killer cell lectin-like receptor, subfamily A, member 2", "gene_symbol": "[\"Klra2\"]", "do": null }, { "gene_id": 16634, "description": "killer cell lectin-like receptor, subfamily A, member 3", "gene_symbol": "[\"Klra3\"]", "do": null }, { "gene_id": 16635, "description": "killer cell lectin-like receptor, subfamily A, member 4", "gene_symbol": "[\"Klra4\"]", "do": null }, { "gene_id": 16636, "description": "killer cell lectin-like receptor, subfamily A, member 5", "gene_symbol": "[\"Klra5\"]", "do": null }, { "gene_id": 16637, "description": "killer cell lectin-like receptor, subfamily A, member 6", "gene_symbol": "[\"Klra6\"]", "do": null }, { "gene_id": 16638, "description": "killer cell lectin-like receptor, subfamily A, member 7", "gene_symbol": "[\"Klra7\"]", "do": null }, { "gene_id": 16639, "description": "killer cell lectin-like receptor, subfamily A, member 8", "gene_symbol": "[\"Klra8\"]", "do": null }, { "gene_id": 16643, "description": "killer cell lectin-like receptor, subfamily D, member 1", "gene_symbol": "[\"Klrd1\"]", "do": null }, { "gene_id": 16644, "description": "kininogen 1", "gene_symbol": "[\"Kng1\"]", "do": null }, { "gene_id": 16646, "description": "karyopherin subunit alpha 1", "gene_symbol": "[\"Kpna1\"]", "do": null }, { "gene_id": 16650, "description": "karyopherin subunit alpha 6", "gene_symbol": "[\"Kpna6\"]", "do": null }, { "gene_id": 16653, "description": "Kras proto-oncogene, GTPase", "gene_symbol": "[\"Kras\"]", "do": "[{\"label\":\"Noonan syndrome 3\",\"id\":\"DOID:0060581\"},{\"label\":\"arteriovenous malformations of the brain\",\"id\":\"DOID:0060688\"},{\"label\":\"endometriosis\",\"id\":\"DOID:289\"},{\"label\":\"intrahepatic cholangiocarcinoma\",\"id\":\"DOID:4928\"},{\"label\":\"juvenile myelomonocytic leukemia\",\"id\":\"DOID:0050458\"},{\"label\":\"lung cancer\",\"id\":\"DOID:1324\"},{\"label\":\"pancreatic carcinoma\",\"id\":\"DOID:4905\"},{\"label\":\"prostate cancer\",\"id\":\"DOID:10283\"}]" }, { "gene_id": 16656, "description": "human immunodeficiency virus type I enhancer binding protein 3", "gene_symbol": "[\"Hivep3\"]", "do": null }, { "gene_id": 16668, "description": "keratin 18", "gene_symbol": "[\"Krt18\"]", "do": "[{\"label\":\"hepatocellular carcinoma\",\"id\":\"DOID:684\"},{\"label\":\"metabolic dysfunction-associated steatohepatitis\",\"id\":\"DOID:0080547\"}]" }, { "gene_id": 16669, "description": "keratin 19", "gene_symbol": "[\"Krt19\"]", "do": null }, { "gene_id": 16678, "description": "keratin 1", "gene_symbol": "[\"Krt1\"]", "do": "[{\"label\":\"epidermolytic hyperkeratosis\",\"id\":\"DOID:4603\"}]" }, { "gene_id": 16681, "description": "keratin 2", "gene_symbol": "[\"Krt2\"]", "do": "[{\"label\":\"bullous congenital ichthyosiform erythroderma\",\"id\":\"DOID:0060877\"}]" }, { "gene_id": 16691, "description": "keratin 8", "gene_symbol": "[\"Krt8\"]", "do": null }, { "gene_id": 16709, "description": "kinectin 1", "gene_symbol": "[\"Ktn1\"]", "do": null }, { "gene_id": 16728, "description": "L1 cell adhesion molecule", "gene_symbol": "[\"L1cam\"]", "do": "[{\"label\":\"MASA syndrome\",\"id\":\"DOID:0060246\"}]" }, { "gene_id": 16763, "description": "ladinin", "gene_symbol": "[\"Lad1\"]", "do": null }, { "gene_id": 16765, "description": "stathmin 1", "gene_symbol": "[\"Stmn1\"]", "do": null }, { "gene_id": 16768, "description": "lymphocyte-activation gene 3", "gene_symbol": "[\"Lag3\"]", "do": null }, { "gene_id": 16769, "description": "desmoglein 4", "gene_symbol": "[\"Dsg4\"]", "do": "[{\"label\":\"hypotrichosis 6\",\"id\":\"DOID:0110703\"}]" }, { "gene_id": 16770, "description": "lactalbumin, alpha", "gene_symbol": "[\"Lalba\"]", "do": null }, { "gene_id": 16772, "description": "laminin, alpha 1", "gene_symbol": "[\"Lama1\"]", "do": null }, { "gene_id": 16773, "description": "laminin, alpha 2", "gene_symbol": "[\"Lama2\"]", "do": "[{\"label\":\"congenital merosin-deficient muscular dystrophy 1A\",\"id\":\"DOID:0110636\"}]" }, { "gene_id": 16774, "description": "laminin, alpha 3", "gene_symbol": "[\"Lama3\"]", "do": "[{\"label\":\"junctional epidermolysis bullosa non-Herlitz type\",\"id\":\"DOID:0060738\"},{\"label\":\"junctional epidermolysis bullosa\",\"id\":\"DOID:3209\"}]" }, { "gene_id": 16775, "description": "laminin, alpha 4", "gene_symbol": "[\"Lama4\"]", "do": null }, { "gene_id": 16776, "description": "laminin, alpha 5", "gene_symbol": "[\"Lama5\"]", "do": "[{\"label\":\"cystic kidney disease\",\"id\":\"DOID:2975\"}]" }, { "gene_id": 16777, "description": "laminin B1", "gene_symbol": "[\"Lamb1\"]", "do": null }, { "gene_id": 16779, "description": "laminin, beta 2", "gene_symbol": "[\"Lamb2\"]", "do": "[{\"label\":\"Pierson syndrome\",\"id\":\"DOID:0060852\"},{\"label\":\"nephrosis\",\"id\":\"DOID:2527\"}]" }, { "gene_id": 16780, "description": "laminin, beta 3", "gene_symbol": "[\"Lamb3\"]", "do": "[{\"label\":\"junctional epidermolysis bullosa Herlitz type\",\"id\":\"DOID:0060737\"},{\"label\":\"junctional epidermolysis bullosa non-Herlitz type\",\"id\":\"DOID:0060738\"}]" }, { "gene_id": 16782, "description": "laminin, gamma 2", "gene_symbol": "[\"Lamc2\"]", "do": "[{\"label\":\"junctional epidermolysis bullosa Herlitz type\",\"id\":\"DOID:0060737\"},{\"label\":\"junctional epidermolysis bullosa non-Herlitz type\",\"id\":\"DOID:0060738\"}]" }, { "gene_id": 16783, "description": "lysosomal-associated membrane protein 1", "gene_symbol": "[\"Lamp1\"]", "do": null }, { "gene_id": 16784, "description": "lysosomal-associated membrane protein 2", "gene_symbol": "[\"Lamp2\"]", "do": "[{\"label\":\"Danon disease\",\"id\":\"DOID:0050437\"}]" }, { "gene_id": 16790, "description": "alanyl aminopeptidase, membrane", "gene_symbol": "[\"Anpep\"]", "do": null }, { "gene_id": 16795, "description": "LARGE xylosyl- and glucuronyltransferase 1", "gene_symbol": "[\"Large1\"]", "do": "[{\"label\":\"facioscapulohumeral muscular dystrophy\",\"id\":\"DOID:11727\"},{\"label\":\"muscular dystrophy-dystroglycanopathy type B1\",\"id\":\"DOID:0050588\"},{\"label\":\"muscular dystrophy-dystroglycanopathy type B6\",\"id\":\"DOID:0110637\"}]" }, { "gene_id": 16796, "description": "LIM and SH3 protein 1", "gene_symbol": "[\"Lasp1\"]", "do": null }, { "gene_id": 16798, "description": "large tumor suppressor", "gene_symbol": "[\"Lats1\"]", "do": null }, { "gene_id": 16800, "description": "Rho/Rac guanine nucleotide exchange factor 2", "gene_symbol": "[\"Arhgef2\"]", "do": "[{\"label\":\"neurodevelopmental disorder with midbrain and hindbrain malformations\",\"id\":\"DOID:0080312\"}]" }, { "gene_id": 16801, "description": "Rho guanine nucleotide exchange factor 1", "gene_symbol": "[\"Arhgef1\"]", "do": null }, { "gene_id": 16803, "description": "lipopolysaccharide binding protein", "gene_symbol": "[\"Lbp\"]", "do": null }, { "gene_id": 16816, "description": "lecithin cholesterol acyltransferase", "gene_symbol": "[\"Lcat\"]", "do": "[{\"label\":\"Norum disease\",\"id\":\"DOID:1391\"}]" }, { "gene_id": 16819, "description": "lipocalin 2", "gene_symbol": "[\"Lcn2\"]", "do": null }, { "gene_id": 16820, "description": "lipocalin 3", "gene_symbol": "[\"Lcn3\"]", "do": null }, { "gene_id": 16825, "description": "LIM domain binding 1", "gene_symbol": "[\"Ldb1\"]", "do": "[{\"label\":\"nail-patella syndrome\",\"id\":\"DOID:9467\"}]" }, { "gene_id": 16828, "description": "lactate dehydrogenase A", "gene_symbol": "[\"Ldha\"]", "do": null }, { "gene_id": 16835, "description": "low density lipoprotein receptor", "gene_symbol": "[\"Ldlr\"]", "do": "[{\"label\":\"familial hypercholesterolemia\",\"id\":\"DOID:13810\"},{\"label\":\"steatotic liver disease\",\"id\":\"DOID:9452\"}]" }, { "gene_id": 16840, "description": "chondromodulin", "gene_symbol": "[\"Cnmd\"]", "do": null }, { "gene_id": 16846, "description": "leptin", "gene_symbol": "[\"Lep\"]", "do": "[{\"label\":\"abdominal obesity-metabolic syndrome 1\",\"id\":\"DOID:14221\"},{\"label\":\"abdominal obesity-metabolic syndrome\",\"id\":\"DOID:0060611\"},{\"label\":\"metabolic dysfunction-associated steatotic liver disease\",\"id\":\"DOID:0080208\"},{\"label\":\"obesity\",\"id\":\"DOID:9970\"},{\"label\":\"steatotic liver disease\",\"id\":\"DOID:9452\"},{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 16847, "description": "leptin receptor", "gene_symbol": "[\"Lepr\"]", "do": "[{\"label\":\"metabolic dysfunction-associated steatotic liver disease\",\"id\":\"DOID:0080208\"},{\"label\":\"obesity\",\"id\":\"DOID:9970\"},{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 16848, "description": "LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase", "gene_symbol": "[\"Lfng\"]", "do": null }, { "gene_id": 16859, "description": "lectin, galactose binding, soluble 9", "gene_symbol": "[\"Lgals9\"]", "do": null }, { "gene_id": 16867, "description": "luteinizing hormone/choriogonadotropin receptor", "gene_symbol": "[\"Lhcgr\"]", "do": null }, { "gene_id": 16878, "description": "leukemia inhibitory factor", "gene_symbol": "[\"Lif\"]", "do": null }, { "gene_id": 16880, "description": "LIF receptor alpha", "gene_symbol": "[\"Lifr\"]", "do": "[{\"label\":\"congenital anomalies of kidney and urinary tract\",\"id\":\"DOID:0080205\"}]" }, { "gene_id": 16885, "description": "LIM domain kinase 1", "gene_symbol": "[\"Limk1\"]", "do": "[{\"label\":\"Williams-Beuren syndrome\",\"id\":\"DOID:1928\"}]" }, { "gene_id": 16886, "description": "LIM domain kinase 2", "gene_symbol": "[\"Limk2\"]", "do": null }, { "gene_id": 16889, "description": "lysosomal A, lysosomal acid type", "gene_symbol": "[\"Lipa\"]", "do": "[{\"label\":\"Wolman disease\",\"id\":\"DOID:14497\"},{\"label\":\"lysosomal acid lipase deficiency\",\"id\":\"DOID:0080217\"}]" }, { "gene_id": 16891, "description": "lipase G, endothelial type", "gene_symbol": "[\"Lipg\"]", "do": null }, { "gene_id": 16898, "description": "ribosomal protein S2", "gene_symbol": "[\"Rps2\"]", "do": null }, { "gene_id": 16905, "description": "lamin A", "gene_symbol": "[\"Lmna\"]", "do": "[{\"label\":\"Charcot-Marie-Tooth disease type 2B1\",\"id\":\"DOID:0110156\"},{\"label\":\"Emery-Dreifuss muscular dystrophy\",\"id\":\"DOID:11726\"},{\"label\":\"achalasia\",\"id\":\"DOID:9164\"},{\"label\":\"congenital muscular dystrophy due to LMNA mutation\",\"id\":\"DOID:0110640\"},{\"label\":\"dilated cardiomyopathy 1A\",\"id\":\"DOID:0110425\"},{\"label\":\"otitis media\",\"id\":\"DOID:10754\"},{\"label\":\"progeria\",\"id\":\"DOID:3911\"}]" }, { "gene_id": 16906, "description": "lamin B1", "gene_symbol": "[\"Lmnb1\"]", "do": "[{\"label\":\"typical adult-onset autosomal dominant demyelinating leukodystrophy\",\"id\":\"DOID:0060785\"}]" }, { "gene_id": 16907, "description": "lamin B2", "gene_symbol": "[\"Lmnb2\"]", "do": null }, { "gene_id": 16924, "description": "ligand of numb-protein X 1", "gene_symbol": "[\"Lnx1\"]", "do": null }, { "gene_id": 16948, "description": "lysyl oxidase", "gene_symbol": "[\"Lox\"]", "do": "[{\"label\":\"Menkes disease\",\"id\":\"DOID:1838\"},{\"label\":\"Williams-Beuren syndrome\",\"id\":\"DOID:1928\"}]" }, { "gene_id": 16950, "description": "lysyl oxidase-like 3", "gene_symbol": "[\"Loxl3\"]", "do": null }, { "gene_id": 16956, "description": "lipoprotein lipase", "gene_symbol": "[\"Lpl\"]", "do": "[{\"label\":\"familial lipoprotein lipase deficiency\",\"id\":\"DOID:14118\"}]" }, { "gene_id": 16971, "description": "low density lipoprotein receptor-related protein 1", "gene_symbol": "[\"Lrp1\"]", "do": "[{\"label\":\"Alzheimer's disease\",\"id\":\"DOID:10652\"},{\"label\":\"cardiomyopathy\",\"id\":\"DOID:0050700\"},{\"label\":\"congenital diaphragmatic hernia\",\"id\":\"DOID:3827\"},{\"label\":\"gastroschisis\",\"id\":\"DOID:11044\"},{\"label\":\"omphalocele\",\"id\":\"DOID:0060327\"}]" }, { "gene_id": 16973, "description": "low density lipoprotein receptor-related protein 5", "gene_symbol": "[\"Lrp5\"]", "do": "[{\"label\":\"exudative vitreoretinopathy\",\"id\":\"DOID:0050535\"},{\"label\":\"osteoporosis-pseudoglioma syndrome\",\"id\":\"DOID:0060849\"}]" }, { "gene_id": 16974, "description": "low density lipoprotein receptor-related protein 6", "gene_symbol": "[\"Lrp6\"]", "do": "[{\"label\":\"neural tube defect\",\"id\":\"DOID:0080074\"},{\"label\":\"steatotic liver disease\",\"id\":\"DOID:9452\"}]" }, { "gene_id": 16975, "description": "low density lipoprotein receptor-related protein 8, apolipoprotein e receptor", "gene_symbol": "[\"Lrp8\"]", "do": null }, { "gene_id": 16976, "description": "low density lipoprotein receptor-related protein associated protein 1", "gene_symbol": "[\"Lrpap1\"]", "do": null }, { "gene_id": 16978, "description": "leucine rich repeat (in FLII) interacting protein 1", "gene_symbol": "[\"Lrrfip1\"]", "do": null }, { "gene_id": 16979, "description": "leucine rich repeat protein 1, neuronal", "gene_symbol": "[\"Lrrn1\"]", "do": null }, { "gene_id": 16980, "description": "leucine rich repeat protein 2, neuronal", "gene_symbol": "[\"Lrrn2\"]", "do": null }, { "gene_id": 16981, "description": "leucine rich repeat protein 3, neuronal", "gene_symbol": "[\"Lrrn3\"]", "do": null }, { "gene_id": 16985, "description": "lymphocyte specific 1", "gene_symbol": "[\"Lsp1\"]", "do": null }, { "gene_id": 16992, "description": "lymphotoxin A", "gene_symbol": "[\"Lta\"]", "do": null }, { "gene_id": 16994, "description": "lymphotoxin B", "gene_symbol": "[\"Ltb\"]", "do": null }, { "gene_id": 16995, "description": "leukotriene B4 receptor 1", "gene_symbol": "[\"Ltb4r1\"]", "do": null }, { "gene_id": 16997, "description": "latent transforming growth factor beta binding protein 2", "gene_symbol": "[\"Ltbp2\"]", "do": null }, { "gene_id": 16998, "description": "latent transforming growth factor beta binding protein 3", "gene_symbol": "[\"Ltbp3\"]", "do": "[{\"label\":\"brachyolmia-amelogenesis imperfecta syndrome\",\"id\":\"DOID:0090143\"}]" }, { "gene_id": 17000, "description": "lymphotoxin B receptor", "gene_symbol": "[\"Ltbr\"]", "do": null }, { "gene_id": 17002, "description": "lactotransferrin", "gene_symbol": "[\"Ltf\"]", "do": null }, { "gene_id": 17005, "description": "leukocyte tyrosine kinase", "gene_symbol": "[\"Ltk\"]", "do": null }, { "gene_id": 17022, "description": "lumican", "gene_symbol": "[\"Lum\"]", "do": "[{\"label\":\"Ehlers-Danlos syndrome classic type 1\",\"id\":\"DOID:14720\"}]" }, { "gene_id": 17059, "description": "killer cell lectin-like receptor subfamily B member 1C", "gene_symbol": "[\"Klrb1c\"]", "do": null }, { "gene_id": 17063, "description": "mucin 13, epithelial transmembrane", "gene_symbol": "[\"Muc13\"]", "do": null }, { "gene_id": 17064, "description": "CD93 antigen", "gene_symbol": "[\"Cd93\"]", "do": null }, { "gene_id": 17069, "description": "lymphocyte antigen 6 family member E", "gene_symbol": "[\"Ly6e\"]", "do": null }, { "gene_id": 17075, "description": "epithelial cell adhesion molecule", "gene_symbol": "[\"Epcam\"]", "do": "[{\"label\":\"congenital diarrhea 5 with tufting enteropathy\",\"id\":\"DOID:0060776\"}]" }, { "gene_id": 17076, "description": "lymphocyte antigen 75", "gene_symbol": "[\"Ly75\"]", "do": null }, { "gene_id": 17079, "description": "CD180 antigen", "gene_symbol": "[\"Cd180\"]", "do": null }, { "gene_id": 17082, "description": "interleukin 1 receptor-like 1", "gene_symbol": "[\"Il1rl1\"]", "do": null }, { "gene_id": 17084, "description": "lymphocyte antigen 86", "gene_symbol": "[\"Ly86\"]", "do": null }, { "gene_id": 17085, "description": "lymphocyte antigen 9", "gene_symbol": "[\"Ly9\"]", "do": null }, { "gene_id": 17086, "description": "natural cytotoxicity triggering receptor 1", "gene_symbol": "[\"Ncr1\"]", "do": null }, { "gene_id": 17087, "description": "lymphocyte antigen 96", "gene_symbol": "[\"Ly96\"]", "do": null }, { "gene_id": 17095, "description": "lymphoblastomic leukemia 1", "gene_symbol": "[\"Lyl1\"]", "do": null }, { "gene_id": 17096, "description": "Lyn proto-oncogene, Src family tyrosine kinase", "gene_symbol": "[\"Lyn\"]", "do": "[{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 17105, "description": "lysozyme 2", "gene_symbol": "[\"Lyz2\"]", "do": null }, { "gene_id": 17110, "description": "lysozyme 1", "gene_symbol": "[\"Lyz1\"]", "do": null }, { "gene_id": 17112, "description": "transmembrane 4 superfamily member 1", "gene_symbol": "[\"Tm4sf1\"]", "do": null }, { "gene_id": 17113, "description": "mannose-6-phosphate receptor, cation dependent", "gene_symbol": "[\"M6pr\"]", "do": null }, { "gene_id": 17126, "description": "SMAD family member 2", "gene_symbol": "[\"Smad2\"]", "do": null }, { "gene_id": 17128, "description": "SMAD family member 4", "gene_symbol": "[\"Smad4\"]", "do": "[{\"label\":\"juvenile polyposis syndrome\",\"id\":\"DOID:0050787\"},{\"label\":\"osteogenesis imperfecta\",\"id\":\"DOID:12347\"}]" }, { "gene_id": 17135, "description": "Maf bZIP transcription factor K", "gene_symbol": "[\"Mafk\"]", "do": null }, { "gene_id": 17136, "description": "myelin-associated glycoprotein", "gene_symbol": "[\"Mag\"]", "do": null }, { "gene_id": 17155, "description": "mannosidase 1, alpha", "gene_symbol": "[\"Man1a\"]", "do": null }, { "gene_id": 17156, "description": "mannosidase, alpha, class 1A, member 2", "gene_symbol": "[\"Man1a2\"]", "do": null }, { "gene_id": 17158, "description": "mannosidase 2, alpha 1", "gene_symbol": "[\"Man2a1\"]", "do": "[{\"label\":\"congenital dyserythropoietic anemia\",\"id\":\"DOID:1338\"},{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 17159, "description": "mannosidase 2, alpha B1", "gene_symbol": "[\"Man2b1\"]", "do": "[{\"label\":\"alpha-mannosidosis\",\"id\":\"DOID:3413\"}]" }, { "gene_id": 17160, "description": "mannosidase 2, alpha B2", "gene_symbol": "[\"Man2b2\"]", "do": null }, { "gene_id": 17165, "description": "MAP kinase-activated protein kinase 5", "gene_symbol": "[\"Mapkapk5\"]", "do": null }, { "gene_id": 17167, "description": "macrophage receptor with collagenous structure", "gene_symbol": "[\"Marco\"]", "do": null }, { "gene_id": 17169, "description": "MAP/microtubule affinity regulating kinase 3", "gene_symbol": "[\"Mark3\"]", "do": null }, { "gene_id": 17171, "description": "MAS1 proto-oncogene, G protein-coupled receptor", "gene_symbol": "[\"Mas1\"]", "do": null }, { "gene_id": 17174, "description": "MBL associated serine protease 1", "gene_symbol": "[\"Masp1\"]", "do": null }, { "gene_id": 17175, "description": "MBL associated serine protease 2", "gene_symbol": "[\"Masp2\"]", "do": null }, { "gene_id": 17180, "description": "matrilin 1, cartilage matrix protein", "gene_symbol": "[\"Matn1\"]", "do": null }, { "gene_id": 17181, "description": "matrilin 2", "gene_symbol": "[\"Matn2\"]", "do": null }, { "gene_id": 17182, "description": "matrilin 3", "gene_symbol": "[\"Matn3\"]", "do": "[{\"label\":\"multiple epiphyseal dysplasia 5\",\"id\":\"DOID:0070299\"},{\"label\":\"osteoarthritis\",\"id\":\"DOID:8398\"}]" }, { "gene_id": 17183, "description": "matrilin 4", "gene_symbol": "[\"Matn4\"]", "do": null }, { "gene_id": 17184, "description": "matrin 3", "gene_symbol": "[\"Matr3\"]", "do": "[{\"label\":\"amyotrophic lateral sclerosis type 21\",\"id\":\"DOID:0060212\"}]" }, { "gene_id": 17187, "description": "Max protein", "gene_symbol": "[\"Max\"]", "do": null }, { "gene_id": 17193, "description": "methyl-CpG binding domain protein 4", "gene_symbol": "[\"Mbd4\"]", "do": null }, { "gene_id": 17194, "description": "mannose-binding lectin (protein A) 1", "gene_symbol": "[\"Mbl1\"]", "do": null }, { "gene_id": 17195, "description": "mannose-binding lectin (protein C) 2", "gene_symbol": "[\"Mbl2\"]", "do": null }, { "gene_id": 17196, "description": "myelin basic protein", "gene_symbol": "[\"Mbp\"]", "do": null }, { "gene_id": 17199, "description": "melanocortin 1 receptor", "gene_symbol": "[\"Mc1r\"]", "do": null }, { "gene_id": 17200, "description": "melanocortin 2 receptor", "gene_symbol": "[\"Mc2r\"]", "do": null }, { "gene_id": 17201, "description": "melanocortin 3 receptor", "gene_symbol": "[\"Mc3r\"]", "do": "[{\"label\":\"obesity\",\"id\":\"DOID:9970\"}]" }, { "gene_id": 17202, "description": "melanocortin 4 receptor", "gene_symbol": "[\"Mc4r\"]", "do": "[{\"label\":\"metabolic dysfunction-associated steatohepatitis\",\"id\":\"DOID:0080547\"},{\"label\":\"obesity\",\"id\":\"DOID:9970\"},{\"label\":\"steatotic liver disease\",\"id\":\"DOID:9452\"}]" }, { "gene_id": 17203, "description": "melanocortin 5 receptor", "gene_symbol": "[\"Mc5r\"]", "do": null }, { "gene_id": 17215, "description": "minichromosome maintenance complex component 3", "gene_symbol": "[\"Mcm3\"]", "do": null }, { "gene_id": 17216, "description": "minichromosome maintenance complex component 2", "gene_symbol": "[\"Mcm2\"]", "do": null }, { "gene_id": 17217, "description": "minichromosome maintenance complex component 4", "gene_symbol": "[\"Mcm4\"]", "do": null }, { "gene_id": 17220, "description": "minichromosome maintenance complex component 7", "gene_symbol": "[\"Mcm7\"]", "do": null }, { "gene_id": 17221, "description": "CD46 antigen, complement regulatory protein", "gene_symbol": "[\"Cd46\"]", "do": "[{\"label\":\"age related macular degeneration\",\"id\":\"DOID:10871\"}]" }, { "gene_id": 17222, "description": "anaphase promoting complex subunit 1", "gene_symbol": "[\"Anapc1\"]", "do": null }, { "gene_id": 17224, "description": "mast cell protease 1", "gene_symbol": "[\"Mcpt1\"]", "do": null }, { "gene_id": 17225, "description": "mast cell protease 2", "gene_symbol": "[\"Mcpt2\"]", "do": null }, { "gene_id": 17228, "description": "chymase 1, mast cell", "gene_symbol": "[\"Cma1\"]", "do": null }, { "gene_id": 17231, "description": "mast cell protease 8", "gene_symbol": "[\"Mcpt8\"]", "do": null }, { "gene_id": 17237, "description": "mahogunin, ring finger 1", "gene_symbol": "[\"Mgrn1\"]", "do": null }, { "gene_id": 17250, "description": "ATP-binding cassette, sub-family C member 1", "gene_symbol": "[\"Abcc1\"]", "do": null }, { "gene_id": 17254, "description": "solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2", "gene_symbol": "[\"Slc3a2\"]", "do": null }, { "gene_id": 17257, "description": "methyl CpG binding protein 2", "gene_symbol": "[\"Mecp2\"]", "do": "[{\"label\":\"Rett syndrome\",\"id\":\"DOID:1206\"}]" }, { "gene_id": 17260, "description": "myocyte enhancer factor 2C", "gene_symbol": "[\"Mef2c\"]", "do": null }, { "gene_id": 17261, "description": "myocyte enhancer factor 2D", "gene_symbol": "[\"Mef2d\"]", "do": null }, { "gene_id": 17281, "description": "FYVE and coiled-coil domain containing 1", "gene_symbol": "[\"Fyco1\"]", "do": null }, { "gene_id": 17287, "description": "meprin 1 alpha", "gene_symbol": "[\"Mep1a\"]", "do": null }, { "gene_id": 17288, "description": "meprin 1 beta", "gene_symbol": "[\"Mep1b\"]", "do": null }, { "gene_id": 17289, "description": "MER proto-oncogene tyrosine kinase", "gene_symbol": "[\"Mertk\"]", "do": null }, { "gene_id": 17294, "description": "mesoderm specific transcript", "gene_symbol": "[\"Mest\"]", "do": "[{\"label\":\"Barth syndrome\",\"id\":\"DOID:0050476\"}]" }, { "gene_id": 17295, "description": "met proto-oncogene, receptor tyrosine kinase", "gene_symbol": "[\"Met\"]", "do": "[{\"label\":\"Gilles de la Tourette syndrome\",\"id\":\"DOID:11119\"},{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"breast cancer\",\"id\":\"DOID:1612\"},{\"label\":\"gestational diabetes\",\"id\":\"DOID:11714\"}]" }, { "gene_id": 17304, "description": "milk fat globule EGF and factor V/VIII domain containing", "gene_symbol": "[\"Mfge8\"]", "do": null }, { "gene_id": 17305, "description": "MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase", "gene_symbol": "[\"Mfng\"]", "do": null }, { "gene_id": 17306, "description": "synaptophysin like 2", "gene_symbol": "[\"Sypl2\"]", "do": null }, { "gene_id": 17308, "description": "mannoside acetylglucosaminyltransferase 1", "gene_symbol": "[\"Mgat1\"]", "do": null }, { "gene_id": 17309, "description": "mannoside acetylglucosaminyltransferase 3", "gene_symbol": "[\"Mgat3\"]", "do": null }, { "gene_id": 17311, "description": "kit ligand", "gene_symbol": "[\"Kitl\"]", "do": null }, { "gene_id": 17312, "description": "C-type lectin domain family 10, member A", "gene_symbol": "[\"Clec10a\"]", "do": null }, { "gene_id": 17329, "description": "C-X-C motif chemokine ligand 9", "gene_symbol": "[\"Cxcl9\"]", "do": null }, { "gene_id": 17330, "description": "multiple inositol polyphosphate histidine phosphatase 1", "gene_symbol": "[\"Minpp1\"]", "do": null }, { "gene_id": 17342, "description": "melanogenesis associated transcription factor", "gene_symbol": "[\"Mitf\"]", "do": "[{\"label\":\"Camurati-Engelmann disease\",\"id\":\"DOID:4997\"},{\"label\":\"Tietz syndrome\",\"id\":\"DOID:0090002\"},{\"label\":\"Waardenburg syndrome type 1\",\"id\":\"DOID:0110948\"},{\"label\":\"Waardenburg syndrome type 2A\",\"id\":\"DOID:0110950\"},{\"label\":\"ocular albinism with sensorineural deafness\",\"id\":\"DOID:0090100\"},{\"label\":\"osteopetrosis\",\"id\":\"DOID:13533\"}]" }, { "gene_id": 17345, "description": "antigen identified by monoclonal antibody Ki 67", "gene_symbol": "[\"Mki67\"]", "do": null }, { "gene_id": 17350, "description": "mutL homolog 1", "gene_symbol": "[\"Mlh1\"]", "do": "[{\"label\":\"Lynch syndrome\",\"id\":\"DOID:3883\"}]" }, { "gene_id": 17354, "description": "myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10", "gene_symbol": "[\"Mllt10\"]", "do": null }, { "gene_id": 17364, "description": "transient receptor potential cation channel, subfamily M, member 1", "gene_symbol": "[\"Trpm1\"]", "do": "[{\"label\":\"congenital stationary night blindness 1C\",\"id\":\"DOID:0110867\"}]" }, { "gene_id": 17380, "description": "membrane metallo endopeptidase", "gene_symbol": "[\"Mme\"]", "do": "[{\"label\":\"Alzheimer's disease\",\"id\":\"DOID:10652\"}]" }, { "gene_id": 17381, "description": "matrix metallopeptidase 12", "gene_symbol": "[\"Mmp12\"]", "do": null }, { "gene_id": 17386, "description": "matrix metallopeptidase 13", "gene_symbol": "[\"Mmp13\"]", "do": null }, { "gene_id": 17388, "description": "matrix metallopeptidase 15", "gene_symbol": "[\"Mmp15\"]", "do": null }, { "gene_id": 17389, "description": "matrix metallopeptidase 16", "gene_symbol": "[\"Mmp16\"]", "do": null }, { "gene_id": 17390, "description": "matrix metallopeptidase 2", "gene_symbol": "[\"Mmp2\"]", "do": null }, { "gene_id": 17394, "description": "matrix metallopeptidase 8", "gene_symbol": "[\"Mmp8\"]", "do": null }, { "gene_id": 17395, "description": "matrix metallopeptidase 9", "gene_symbol": "[\"Mmp9\"]", "do": null }, { "gene_id": 17423, "description": "N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2", "gene_symbol": "[\"Ndst2\"]", "do": null }, { "gene_id": 17425, "description": "forkhead box K1", "gene_symbol": "[\"Foxk1\"]", "do": null }, { "gene_id": 17428, "description": "max binding protein", "gene_symbol": "[\"Mnt\"]", "do": "[{\"label\":\"Miller-Dieker lissencephaly syndrome\",\"id\":\"DOID:0060469\"}]" }, { "gene_id": 17441, "description": "myelin oligodendrocyte glycoprotein", "gene_symbol": "[\"Mog\"]", "do": null }, { "gene_id": 17448, "description": "malate dehydrogenase 2, NAD (mitochondrial)", "gene_symbol": "[\"Mdh2\"]", "do": null }, { "gene_id": 17449, "description": "malate dehydrogenase 1, NAD (soluble)", "gene_symbol": "[\"Mdh1\"]", "do": null }, { "gene_id": 17454, "description": "Mov10 RISC complex RNA helicase", "gene_symbol": "[\"Mov10\"]", "do": null }, { "gene_id": 17470, "description": "CD200 molecule", "gene_symbol": "[\"Cd200\"]", "do": "[{\"label\":\"autoimmune disease\",\"id\":\"DOID:417\"}]" }, { "gene_id": 17474, "description": "C-type lectin domain family 4, member d", "gene_symbol": "[\"Clec4d\"]", "do": null }, { "gene_id": 17476, "description": "macrophage expressed gene 1", "gene_symbol": "[\"Mpeg1\"]", "do": null }, { "gene_id": 17480, "description": "Mpl proto-oncogene, thrombopoietin receptor", "gene_symbol": "[\"Mpl\"]", "do": "[{\"label\":\"congenital amegakaryocytic thrombocytopenia\",\"id\":\"DOID:0090118\"}]" }, { "gene_id": 17523, "description": "myeloperoxidase", "gene_symbol": "[\"Mpo\"]", "do": null }, { "gene_id": 17528, "description": "myelin protein zero", "gene_symbol": "[\"Mpz\"]", "do": "[{\"label\":\"Charcot-Marie-Tooth disease type 1B\",\"id\":\"DOID:0110152\"},{\"label\":\"Charcot-Marie-Tooth disease type 3\",\"id\":\"DOID:0050540\"},{\"label\":\"PCWH syndrome\",\"id\":\"DOID:0090111\"},{\"label\":\"neuropathy\",\"id\":\"DOID:870\"}]" }, { "gene_id": 17533, "description": "mannose receptor, C type 1", "gene_symbol": "[\"Mrc1\"]", "do": null }, { "gene_id": 17534, "description": "mannose receptor, C type 2", "gene_symbol": "[\"Mrc2\"]", "do": null }, { "gene_id": 17535, "description": "MRE11A homolog A, double strand break repair nuclease", "gene_symbol": "[\"Mre11a\"]", "do": null }, { "gene_id": 17540, "description": "inositol 1,4,5-triphosphate receptor associated 1", "gene_symbol": "[\"Irag1\"]", "do": null }, { "gene_id": 17686, "description": "mutS homolog 3", "gene_symbol": "[\"Msh3\"]", "do": null }, { "gene_id": 17688, "description": "mutS homolog 6", "gene_symbol": "[\"Msh6\"]", "do": null }, { "gene_id": 17698, "description": "moesin", "gene_symbol": "[\"Msn\"]", "do": null }, { "gene_id": 17700, "description": "myostatin", "gene_symbol": "[\"Mstn\"]", "do": "[{\"label\":\"myostatin-related muscle hypertrophy\",\"id\":\"DOID:0111072\"}]" }, { "gene_id": 17721, "description": "NADH dehydrogenase subunit 5", "gene_symbol": "[\"ND5\"]", "do": null }, { "gene_id": 17754, "description": "microtubule-associated protein 1 A", "gene_symbol": "[\"Map1a\"]", "do": null }, { "gene_id": 17755, "description": "microtubule-associated protein 1B", "gene_symbol": "[\"Map1b\"]", "do": null }, { "gene_id": 17756, "description": "microtubule-associated protein 2", "gene_symbol": "[\"Map2\"]", "do": null }, { "gene_id": 17758, "description": "microtubule-associated protein 4", "gene_symbol": "[\"Map4\"]", "do": null }, { "gene_id": 17760, "description": "microtubule-associated protein 6", "gene_symbol": "[\"Map6\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 17762, "description": "microtubule-associated protein tau", "gene_symbol": "[\"Mapt\"]", "do": null }, { "gene_id": 17773, "description": "melatonin receptor 1A", "gene_symbol": "[\"Mtnr1a\"]", "do": null }, { "gene_id": 17777, "description": "microsomal triglyceride transfer protein", "gene_symbol": "[\"Mttp\"]", "do": null }, { "gene_id": 17829, "description": "mucin 1, transmembrane", "gene_symbol": "[\"Muc1\"]", "do": null }, { "gene_id": 17833, "description": "mucin 5, subtypes A and C, tracheobronchial/gastric", "gene_symbol": "[\"Muc5ac\"]", "do": "[{\"label\":\"dry eye syndrome\",\"id\":\"DOID:10140\"}]" }, { "gene_id": 17836, "description": "murinoglobulin 1", "gene_symbol": "[\"Mug1\"]", "do": null }, { "gene_id": 17837, "description": "murinoglobulin 2", "gene_symbol": "[\"Mug2\"]", "do": null }, { "gene_id": 17842, "description": "major urinary protein 3", "gene_symbol": "[\"Mup3\"]", "do": null }, { "gene_id": 17847, "description": "ubiquitin specific peptidase 34", "gene_symbol": "[\"Usp34\"]", "do": null }, { "gene_id": 17850, "description": "methylmalonyl-Coenzyme A mutase", "gene_symbol": "[\"Mmut\"]", "do": "[{\"label\":\"methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency\",\"id\":\"DOID:0060740\"}]" }, { "gene_id": 17863, "description": "Myb proto-oncogene, transcription factor", "gene_symbol": "[\"Myb\"]", "do": "[{\"label\":\"essential thrombocythemia\",\"id\":\"DOID:2224\"},{\"label\":\"myelofibrosis\",\"id\":\"DOID:4971\"}]" }, { "gene_id": 17869, "description": "Myc proto-oncogene, bHLH transcription factor", "gene_symbol": "[\"Myc\"]", "do": "[{\"label\":\"Burkitt lymphoma\",\"id\":\"DOID:8584\"},{\"label\":\"autosomal dominant polycystic kidney disease\",\"id\":\"DOID:898\"},{\"label\":\"breast cancer\",\"id\":\"DOID:1612\"},{\"label\":\"hepatocellular carcinoma\",\"id\":\"DOID:684\"},{\"label\":\"pancreatic carcinoma\",\"id\":\"DOID:4905\"}]" }, { "gene_id": 17879, "description": "myosin, heavy polypeptide 1, skeletal muscle, adult", "gene_symbol": "[\"Myh1\"]", "do": null }, { "gene_id": 17882, "description": "myosin, heavy polypeptide 2, skeletal muscle, adult", "gene_symbol": "[\"Myh2\"]", "do": null }, { "gene_id": 17883, "description": "myosin, heavy polypeptide 3, skeletal muscle, embryonic", "gene_symbol": "[\"Myh3\"]", "do": null }, { "gene_id": 17884, "description": "myosin, heavy polypeptide 4, skeletal muscle", "gene_symbol": "[\"Myh4\"]", "do": null }, { "gene_id": 17886, "description": "myosin, heavy polypeptide 9, non-muscle", "gene_symbol": "[\"Myh9\"]", "do": "[{\"label\":\"MYH-9 related disease\",\"id\":\"DOID:0060651\"}]" }, { "gene_id": 17888, "description": "myosin, heavy polypeptide 6, cardiac muscle, alpha", "gene_symbol": "[\"Myh6\"]", "do": "[{\"label\":\"dilated cardiomyopathy 1EE\",\"id\":\"DOID:0110453\"},{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"},{\"label\":\"hypertrophic cardiomyopathy 14\",\"id\":\"DOID:0110320\"}]" }, { "gene_id": 17897, "description": "myosin, light polypeptide 3", "gene_symbol": "[\"Myl3\"]", "do": "[{\"label\":\"osteoarthritis\",\"id\":\"DOID:8398\"}]" }, { "gene_id": 17901, "description": "myosin, light polypeptide 1", "gene_symbol": "[\"Myl1\"]", "do": null }, { "gene_id": 17904, "description": "myosin, light polypeptide 6, alkali, smooth muscle and non-muscle", "gene_symbol": "[\"Myl6\"]", "do": null }, { "gene_id": 17913, "description": "myosin IC", "gene_symbol": "[\"Myo1c\"]", "do": null }, { "gene_id": 17918, "description": "myosin VA", "gene_symbol": "[\"Myo5a\"]", "do": "[{\"label\":\"Griscelli syndrome type 1\",\"id\":\"DOID:0060832\"}]" }, { "gene_id": 17920, "description": "myosin VI", "gene_symbol": "[\"Myo6\"]", "do": "[{\"label\":\"autosomal dominant nonsyndromic deafness 22\",\"id\":\"DOID:0110552\"},{\"label\":\"autosomal recessive nonsyndromic deafness 37\",\"id\":\"DOID:0110495\"}]" }, { "gene_id": 17922, "description": "myosin VIIB", "gene_symbol": "[\"Myo7b\"]", "do": null }, { "gene_id": 17926, "description": "myocilin", "gene_symbol": "[\"Myoc\"]", "do": "[{\"label\":\"open-angle glaucoma\",\"id\":\"DOID:1067\"}]" }, { "gene_id": 17929, "description": "myomesin 1", "gene_symbol": "[\"Myom1\"]", "do": null }, { "gene_id": 17930, "description": "myomesin 2", "gene_symbol": "[\"Myom2\"]", "do": null }, { "gene_id": 17931, "description": "protein phosphatase 1, regulatory subunit 12A", "gene_symbol": "[\"Ppp1r12a\"]", "do": null }, { "gene_id": 17933, "description": "myelin transcription factor 1-like", "gene_symbol": "[\"Myt1l\"]", "do": "[{\"label\":\"autosomal dominant intellectual developmental disorder 39\",\"id\":\"DOID:0070069\"}]" }, { "gene_id": 17936, "description": "Ngfi-A binding protein 1", "gene_symbol": "[\"Nab1\"]", "do": null }, { "gene_id": 17938, "description": "nascent polypeptide-associated complex alpha polypeptide", "gene_symbol": "[\"Naca\"]", "do": null }, { "gene_id": 17939, "description": "N-acetyl galactosaminidase, alpha", "gene_symbol": "[\"Naga\"]", "do": null }, { "gene_id": 17948, "description": "NLR family, apoptosis inhibitory protein 2", "gene_symbol": "[\"Naip2\"]", "do": null }, { "gene_id": 17955, "description": "nucleosome assembly protein 1-like 4", "gene_symbol": "[\"Nap1l4\"]", "do": null }, { "gene_id": 17957, "description": "N-ethylmaleimide sensitive fusion protein attachment protein beta", "gene_symbol": "[\"Napb\"]", "do": null }, { "gene_id": 17965, "description": "NBL1, DAN family BMP antagonist", "gene_symbol": "[\"Nbl1\"]", "do": null }, { "gene_id": 17967, "description": "neural cell adhesion molecule 1", "gene_symbol": "[\"Ncam1\"]", "do": null }, { "gene_id": 17968, "description": "neural cell adhesion molecule 2", "gene_symbol": "[\"Ncam2\"]", "do": null }, { "gene_id": 17975, "description": "nucleolin multifunctional protein", "gene_symbol": "[\"Nucleolin\"]", "do": null }, { "gene_id": 17977, "description": "nuclear receptor coactivator 1", "gene_symbol": "[\"Ncoa1\"]", "do": "[{\"label\":\"obesity\",\"id\":\"DOID:9970\"},{\"label\":\"thyroid hormone resistance syndrome\",\"id\":\"DOID:11633\"}]" }, { "gene_id": 17978, "description": "nuclear receptor coactivator 2", "gene_symbol": "[\"Ncoa2\"]", "do": null }, { "gene_id": 17991, "description": "NADH:ubiquinone oxidoreductase subunit A2", "gene_symbol": "[\"Ndufa2\"]", "do": null }, { "gene_id": 17993, "description": "NADH:ubiquinone oxidoreductase core subunit S4", "gene_symbol": "[\"Ndufs4\"]", "do": "[{\"label\":\"Leigh disease\",\"id\":\"DOID:3652\"},{\"label\":\"mitochondrial complex I deficiency\",\"id\":\"DOID:0060536\"}]" }, { "gene_id": 17996, "description": "nebulin", "gene_symbol": "[\"Neb\"]", "do": "[{\"label\":\"nemaline myopathy 2\",\"id\":\"DOID:0110928\"}]" }, { "gene_id": 17997, "description": "neural precursor cell expressed, developmentally down-regulated gene 1", "gene_symbol": "[\"Nedd1\"]", "do": null }, { "gene_id": 17999, "description": "neural precursor cell expressed, developmentally down-regulated 4", "gene_symbol": "[\"Nedd4\"]", "do": null }, { "gene_id": 18007, "description": "neogenin", "gene_symbol": "[\"Neo1\"]", "do": null }, { "gene_id": 18010, "description": "neuraminidase 1", "gene_symbol": "[\"Neu1\"]", "do": "[{\"label\":\"glycoproteinosis\",\"id\":\"DOID:3343\"}]" }, { "gene_id": 18015, "description": "neurofibromin 1", "gene_symbol": "[\"Nf1\"]", "do": "[{\"label\":\"juvenile myelomonocytic leukemia\",\"id\":\"DOID:0050458\"},{\"label\":\"neurofibromatosis 1\",\"id\":\"DOID:0111253\"}]" }, { "gene_id": 18019, "description": "nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2", "gene_symbol": "[\"Nfatc2\"]", "do": null }, { "gene_id": 18023, "description": "nuclear factor, erythroid derived 2,-like 1", "gene_symbol": "[\"Nfe2l1\"]", "do": "[{\"label\":\"hepatocellular carcinoma\",\"id\":\"DOID:684\"},{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 18024, "description": "nuclear factor, erythroid derived 2, like 2", "gene_symbol": "[\"Nfe2l2\"]", "do": null }, { "gene_id": 18027, "description": "nuclear factor I/A", "gene_symbol": "[\"Nfia\"]", "do": null }, { "gene_id": 18028, "description": "nuclear factor I/B", "gene_symbol": "[\"Nfib\"]", "do": null }, { "gene_id": 18032, "description": "nuclear factor I/X", "gene_symbol": "[\"Nfix\"]", "do": "[{\"label\":\"Scheuermann's disease\",\"id\":\"DOID:13300\"},{\"label\":\"Sotos syndrome 2\",\"id\":\"DOID:0112102\"}]" }, { "gene_id": 18033, "description": "nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105", "gene_symbol": "[\"Nfkb1\"]", "do": null }, { "gene_id": 18039, "description": "neurofilament, light polypeptide", "gene_symbol": "[\"Nefl\"]", "do": "[{\"label\":\"Charcot-Marie-Tooth disease type 2E\",\"id\":\"DOID:0110165\"}]" }, { "gene_id": 18040, "description": "neurofilament, medium polypeptide", "gene_symbol": "[\"Nefm\"]", "do": null }, { "gene_id": 18048, "description": "kallikrein 1-related pepidase b4", "gene_symbol": "[\"Klk1b4\"]", "do": null }, { "gene_id": 18049, "description": "nerve growth factor", "gene_symbol": "[\"Ngf\"]", "do": null }, { "gene_id": 18050, "description": "kallikrein 1-related peptidase b3", "gene_symbol": "[\"Klk1b3\"]", "do": null }, { "gene_id": 18053, "description": "nerve growth factor receptor (TNFR superfamily, member 16)", "gene_symbol": "[\"Ngfr\"]", "do": null }, { "gene_id": 18054, "description": "neutrophilic granule protein", "gene_symbol": "[\"Ngp\"]", "do": null }, { "gene_id": 18073, "description": "nidogen 1", "gene_symbol": "[\"Nid1\"]", "do": null }, { "gene_id": 18074, "description": "nidogen 2", "gene_symbol": "[\"Nid2\"]", "do": null }, { "gene_id": 18081, "description": "ninjurin 1", "gene_symbol": "[\"Ninj1\"]", "do": null }, { "gene_id": 18099, "description": "nemo like kinase", "gene_symbol": "[\"Nlk\"]", "do": null }, { "gene_id": 18100, "description": "mitochondrial ribosomal protein L40", "gene_symbol": "[\"Mrpl40\"]", "do": null }, { "gene_id": 18101, "description": "neuromedin B receptor", "gene_symbol": "[\"Nmbr\"]", "do": null }, { "gene_id": 18106, "description": "CD244 molecule A", "gene_symbol": "[\"Cd244a\"]", "do": null }, { "gene_id": 18107, "description": "N-myristoyltransferase 1", "gene_symbol": "[\"Nmt1\"]", "do": null }, { "gene_id": 18109, "description": "Mycn proto-oncogene, bHLH transcription factor", "gene_symbol": "[\"Mycn\"]", "do": null }, { "gene_id": 18119, "description": "nodal growth differentiation factor", "gene_symbol": "[\"Nodal\"]", "do": null }, { "gene_id": 18121, "description": "noggin", "gene_symbol": "[\"Nog\"]", "do": "[{\"label\":\"esophageal atresia/tracheoesophageal fistula\",\"id\":\"DOID:0080171\"}]" }, { "gene_id": 18127, "description": "nitric oxide synthase 3, endothelial cell", "gene_symbol": "[\"Nos3\"]", "do": "[{\"label\":\"aortic valve disease\",\"id\":\"DOID:62\"},{\"label\":\"essential hypertension\",\"id\":\"DOID:10825\"},{\"label\":\"persistent fetal circulation syndrome\",\"id\":\"DOID:13042\"}]" }, { "gene_id": 18128, "description": "notch 1", "gene_symbol": "[\"Notch1\"]", "do": null }, { "gene_id": 18129, "description": "notch 2", "gene_symbol": "[\"Notch2\"]", "do": "[{\"label\":\"Hajdu-Cheney syndrome\",\"id\":\"DOID:2736\"},{\"label\":\"pre-eclampsia\",\"id\":\"DOID:10591\"}]" }, { "gene_id": 18130, "description": "integrator complex subunit 6", "gene_symbol": "[\"Ints6\"]", "do": null }, { "gene_id": 18131, "description": "notch 3", "gene_symbol": "[\"Notch3\"]", "do": "[{\"label\":\"acute lymphoblastic leukemia\",\"id\":\"DOID:9952\"},{\"label\":\"autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1\",\"id\":\"DOID:0111035\"}]" }, { "gene_id": 18132, "description": "notch 4", "gene_symbol": "[\"Notch4\"]", "do": "[{\"label\":\"arteriovenous malformations of the brain\",\"id\":\"DOID:0060688\"}]" }, { "gene_id": 18133, "description": "cellular communication network factor 3", "gene_symbol": "[\"Ccn3\"]", "do": null }, { "gene_id": 18139, "description": "zinc finger protein 638", "gene_symbol": "[\"Zfp638\"]", "do": null }, { "gene_id": 18141, "description": "nucleoporin 50", "gene_symbol": "[\"Nup50\"]", "do": null }, { "gene_id": 18143, "description": "neuronal PAS domain protein 2", "gene_symbol": "[\"Npas2\"]", "do": null }, { "gene_id": 18145, "description": "NPC intracellular cholesterol transporter 1", "gene_symbol": "[\"Npc1\"]", "do": "[{\"label\":\"Niemann-Pick disease type C1\",\"id\":\"DOID:0070113\"},{\"label\":\"Niemann-Pick disease\",\"id\":\"DOID:14504\"}]" }, { "gene_id": 18146, "description": "neural proliferation, differentiation and control 1", "gene_symbol": "[\"Npdc1\"]", "do": null }, { "gene_id": 18148, "description": "nucleophosmin 1", "gene_symbol": "[\"Npm1\"]", "do": "[{\"label\":\"myelodysplastic syndrome\",\"id\":\"DOID:0050908\"}]" }, { "gene_id": 18160, "description": "natriuretic peptide receptor 1", "gene_symbol": "[\"Npr1\"]", "do": null }, { "gene_id": 18162, "description": "natriuretic peptide receptor 3", "gene_symbol": "[\"Npr3\"]", "do": "[{\"label\":\"bone disease\",\"id\":\"DOID:0080001\"}]" }, { "gene_id": 18163, "description": "catenin delta 2", "gene_symbol": "[\"Ctnnd2\"]", "do": null }, { "gene_id": 18164, "description": "neuronal pentraxin 1", "gene_symbol": "[\"Nptx1\"]", "do": null }, { "gene_id": 18166, "description": "neuropeptide Y receptor Y1", "gene_symbol": "[\"Npy1r\"]", "do": "[{\"label\":\"obesity\",\"id\":\"DOID:9970\"}]" }, { "gene_id": 18167, "description": "neuropeptide Y receptor Y2", "gene_symbol": "[\"Npy2r\"]", "do": null }, { "gene_id": 18168, "description": "neuropeptide Y receptor Y5", "gene_symbol": "[\"Npy5r\"]", "do": null }, { "gene_id": 18169, "description": "neuropeptide Y receptor Y6", "gene_symbol": "[\"Npy6r\"]", "do": null }, { "gene_id": 18173, "description": "solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1", "gene_symbol": "[\"Slc11a1\"]", "do": null }, { "gene_id": 18174, "description": "solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2", "gene_symbol": "[\"Slc11a2\"]", "do": null }, { "gene_id": 18175, "description": "nebulin-related anchoring protein", "gene_symbol": "[\"Nrap\"]", "do": null }, { "gene_id": 18186, "description": "neuropilin 1", "gene_symbol": "[\"Nrp1\"]", "do": "[{\"label\":\"retinal vein occlusion\",\"id\":\"DOID:1727\"}]" }, { "gene_id": 18187, "description": "neuropilin 2", "gene_symbol": "[\"Nrp2\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 18189, "description": "neurexin I", "gene_symbol": "[\"Nrxn1\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 18190, "description": "neurexin II", "gene_symbol": "[\"Nrxn2\"]", "do": null }, { "gene_id": 18191, "description": "neurexin III", "gene_symbol": "[\"Nrxn3\"]", "do": null }, { "gene_id": 18195, "description": "N-ethylmaleimide sensitive fusion protein", "gene_symbol": "[\"Nsf\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 18198, "description": "muscle, skeletal, receptor tyrosine kinase", "gene_symbol": "[\"Musk\"]", "do": "[{\"label\":\"congenital myasthenic syndrome 9\",\"id\":\"DOID:0110670\"}]" }, { "gene_id": 18205, "description": "neurotrophin 3", "gene_symbol": "[\"Ntf3\"]", "do": "[{\"label\":\"atrial heart septal defect 1\",\"id\":\"DOID:0110106\"},{\"label\":\"tetralogy of Fallot\",\"id\":\"DOID:6419\"}]" }, { "gene_id": 18207, "description": "nth (endonuclease III)-like 1 (E.coli)", "gene_symbol": "[\"Nthl1\"]", "do": null }, { "gene_id": 18208, "description": "netrin 1", "gene_symbol": "[\"Ntn1\"]", "do": null }, { "gene_id": 18209, "description": "netrin 3", "gene_symbol": "[\"Ntn3\"]", "do": null }, { "gene_id": 18211, "description": "neurotrophic tyrosine kinase, receptor, type 1", "gene_symbol": "[\"Ntrk1\"]", "do": "[{\"label\":\"hereditary sensory and autonomic neuropathy\",\"id\":\"DOID:0050548\"}]" }, { "gene_id": 18212, "description": "neurotrophic tyrosine kinase, receptor, type 2", "gene_symbol": "[\"Ntrk2\"]", "do": null }, { "gene_id": 18213, "description": "neurotrophic tyrosine kinase, receptor, type 3", "gene_symbol": "[\"Ntrk3\"]", "do": null }, { "gene_id": 18214, "description": "discoidin domain receptor family, member 2", "gene_symbol": "[\"Ddr2\"]", "do": null }, { "gene_id": 18216, "description": "neurotensin receptor 1", "gene_symbol": "[\"Ntsr1\"]", "do": null }, { "gene_id": 18220, "description": "nucleobindin 1", "gene_symbol": "[\"Nucb1\"]", "do": null }, { "gene_id": 18223, "description": "numb-like", "gene_symbol": "[\"Numbl\"]", "do": null }, { "gene_id": 18226, "description": "nucleoporin 62", "gene_symbol": "[\"Nup62\"]", "do": null }, { "gene_id": 18231, "description": "neurexophilin 1", "gene_symbol": "[\"Nxph1\"]", "do": null }, { "gene_id": 18232, "description": "neurexophilin 2", "gene_symbol": "[\"Nxph2\"]", "do": null }, { "gene_id": 18241, "description": "G protein-coupled receptor 143", "gene_symbol": "[\"Gpr143\"]", "do": "[{\"label\":\"ocular albinism 1\",\"id\":\"DOID:0050633\"}]" }, { "gene_id": 18256, "description": "otoconin 90", "gene_symbol": "[\"Oc90\"]", "do": null }, { "gene_id": 18293, "description": "oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)", "gene_symbol": "[\"Ogdh\"]", "do": null }, { "gene_id": 18294, "description": "8-oxoguanine DNA-glycosylase 1", "gene_symbol": "[\"Ogg1\"]", "do": null }, { "gene_id": 18295, "description": "osteoglycin", "gene_symbol": "[\"Ogn\"]", "do": null }, { "gene_id": 18300, "description": "FAM3 metabolism regulating signaling molecule D", "gene_symbol": "[\"Fam3d\"]", "do": null }, { "gene_id": 18302, "description": "oncoprotein induced transcript 3", "gene_symbol": "[\"Oit3\"]", "do": null }, { "gene_id": 18307, "description": "olfactory receptor family 2 subfamily Y member 1B", "gene_symbol": "[\"Or2y1b\"]", "do": null }, { "gene_id": 18310, "description": "olfactory receptor family 2 subfamily A member 7", "gene_symbol": "[\"Or2a7\"]", "do": null }, { "gene_id": 18312, "description": "olfactory receptor family 2 subfamily C member 1", "gene_symbol": "[\"Or2c1\"]", "do": null }, { "gene_id": 18315, "description": "olfactory receptor family 7 subfamily E member 178", "gene_symbol": "[\"Or7e178\"]", "do": null }, { "gene_id": 18316, "description": "olfactory receptor family 7 subfamily A member 40", "gene_symbol": "[\"Or7a40\"]", "do": null }, { "gene_id": 18322, "description": "olfactory receptor family 1 subfamily M member 1", "gene_symbol": "[\"Or1m1\"]", "do": null }, { "gene_id": 18328, "description": "olfactory receptor family 1 subfamily J member 1", "gene_symbol": "[\"Or1j1\"]", "do": null }, { "gene_id": 18348, "description": "olfactory receptor family 6 subfamily E member 1", "gene_symbol": "[\"Or6e1\"]", "do": null }, { "gene_id": 18349, "description": "olfactory receptor family 6 subfamily Z member 7", "gene_symbol": "[\"Or6z7\"]", "do": null }, { "gene_id": 18372, "description": "olfactory receptor family 7 subfamily A member 42", "gene_symbol": "[\"Or7a42\"]", "do": null }, { "gene_id": 18373, "description": "olfactory receptor family 10 subfamily P member 22", "gene_symbol": "[\"Or10p22\"]", "do": null }, { "gene_id": 18377, "description": "oligodendrocyte myelin glycoprotein", "gene_symbol": "[\"Omg\"]", "do": null }, { "gene_id": 18383, "description": "tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)", "gene_symbol": "[\"Tnfrsf11b\"]", "do": "[{\"label\":\"osteoporosis\",\"id\":\"DOID:11476\"}]" }, { "gene_id": 18386, "description": "opioid receptor, delta 1", "gene_symbol": "[\"Oprd1\"]", "do": null }, { "gene_id": 18387, "description": "opioid receptor, kappa 1", "gene_symbol": "[\"Oprk1\"]", "do": null }, { "gene_id": 18389, "description": "opioid receptor-like 1", "gene_symbol": "[\"Oprl1\"]", "do": null }, { "gene_id": 18390, "description": "opioid receptor, mu 1", "gene_symbol": "[\"Oprm1\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 18399, "description": "solute carrier family 22 (organic anion transporter), member 6", "gene_symbol": "[\"Slc22a6\"]", "do": null }, { "gene_id": 18405, "description": "orosomucoid 1", "gene_symbol": "[\"Orm1\"]", "do": null }, { "gene_id": 18406, "description": "orosomucoid 2", "gene_symbol": "[\"Orm2\"]", "do": null }, { "gene_id": 18412, "description": "sequestosome 1", "gene_symbol": "[\"Sqstm1\"]", "do": "[{\"label\":\"Paget's disease of bone\",\"id\":\"DOID:5408\"}]" }, { "gene_id": 18413, "description": "oncostatin M", "gene_symbol": "[\"Osm\"]", "do": null }, { "gene_id": 18414, "description": "oncostatin M receptor", "gene_symbol": "[\"Osmr\"]", "do": null }, { "gene_id": 18415, "description": "heat shock protein 4 like", "gene_symbol": "[\"Hspa4l\"]", "do": null }, { "gene_id": 18419, "description": "otogelin", "gene_symbol": "[\"Otog\"]", "do": "[{\"label\":\"autosomal recessive nonsyndromic deafness 18B\",\"id\":\"DOID:0110474\"}]" }, { "gene_id": 18430, "description": "oxytocin receptor", "gene_symbol": "[\"Oxtr\"]", "do": null }, { "gene_id": 18431, "description": "oculocutaneous albinism II", "gene_symbol": "[\"Oca2\"]", "do": "[{\"label\":\"oculocutaneous albinism\",\"id\":\"DOID:0050632\"}]" }, { "gene_id": 18432, "description": "MYB binding protein (P160) 1a", "gene_symbol": "[\"Mybbp1a\"]", "do": null }, { "gene_id": 18436, "description": "purinergic receptor P2X, ligand-gated ion channel, 1", "gene_symbol": "[\"P2rx1\"]", "do": null }, { "gene_id": 18438, "description": "purinergic receptor P2X, ligand-gated ion channel 4", "gene_symbol": "[\"P2rx4\"]", "do": null }, { "gene_id": 18439, "description": "purinergic receptor P2X, ligand-gated ion channel, 7", "gene_symbol": "[\"P2rx7\"]", "do": null }, { "gene_id": 18440, "description": "purinergic receptor P2X, ligand-gated ion channel, 6", "gene_symbol": "[\"P2rx6\"]", "do": null }, { "gene_id": 18441, "description": "purinergic receptor P2Y, G-protein coupled 1", "gene_symbol": "[\"P2ry1\"]", "do": null }, { "gene_id": 18442, "description": "purinergic receptor P2Y, G-protein coupled 2", "gene_symbol": "[\"P2ry2\"]", "do": null }, { "gene_id": 18451, "description": "procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha 1 polypeptide", "gene_symbol": "[\"P4ha1\"]", "do": null }, { "gene_id": 18452, "description": "procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha II polypeptide", "gene_symbol": "[\"P4ha2\"]", "do": null }, { "gene_id": 18458, "description": "poly(A) binding protein, cytoplasmic 1", "gene_symbol": "[\"Pabpc1\"]", "do": null }, { "gene_id": 18477, "description": "peroxiredoxin 1", "gene_symbol": "[\"Prdx1\"]", "do": null }, { "gene_id": 18479, "description": "p21 (RAC1) activated kinase 1", "gene_symbol": "[\"Pak1\"]", "do": null }, { "gene_id": 18481, "description": "p21 (RAC1) activated kinase 3", "gene_symbol": "[\"Pak3\"]", "do": "[{\"label\":\"non-syndromic X-linked intellectual disability 30\",\"id\":\"DOID:0112051\"}]" }, { "gene_id": 18483, "description": "paralemmin", "gene_symbol": "[\"Palm\"]", "do": null }, { "gene_id": 18484, "description": "peptidylglycine alpha-amidating monooxygenase", "gene_symbol": "[\"Pam\"]", "do": null }, { "gene_id": 18488, "description": "contactin 3", "gene_symbol": "[\"Cntn3\"]", "do": null }, { "gene_id": 18491, "description": "pregnancy-associated plasma protein A", "gene_symbol": "[\"Pappa\"]", "do": null }, { "gene_id": 18519, "description": "K(lysine) acetyltransferase 2B", "gene_symbol": "[\"Kat2b\"]", "do": null }, { "gene_id": 18521, "description": "poly(rC) binding protein 2", "gene_symbol": "[\"Pcbp2\"]", "do": null }, { "gene_id": 18530, "description": "protocadherin 8", "gene_symbol": "[\"Pcdh8\"]", "do": null }, { "gene_id": 18534, "description": "phosphoenolpyruvate carboxykinase 1, cytosolic", "gene_symbol": "[\"Pck1\"]", "do": null }, { "gene_id": 18536, "description": "pericentriolar material 1", "gene_symbol": "[\"Pcm1\"]", "do": null }, { "gene_id": 18538, "description": "proliferating cell nuclear antigen", "gene_symbol": "[\"Pcna\"]", "do": null }, { "gene_id": 18542, "description": "procollagen C-endopeptidase enhancer protein", "gene_symbol": "[\"Pcolce\"]", "do": null }, { "gene_id": 18548, "description": "proprotein convertase subtilisin/kexin type 1", "gene_symbol": "[\"Pcsk1\"]", "do": "[{\"label\":\"endocrine system disease\",\"id\":\"DOID:28\"},{\"label\":\"obesity\",\"id\":\"DOID:9970\"}]" }, { "gene_id": 18549, "description": "proprotein convertase subtilisin/kexin type 2", "gene_symbol": "[\"Pcsk2\"]", "do": null }, { "gene_id": 18550, "description": "furin, paired basic amino acid cleaving enzyme", "gene_symbol": "[\"Furin\"]", "do": null }, { "gene_id": 18551, "description": "proprotein convertase subtilisin/kexin type 4", "gene_symbol": "[\"Pcsk4\"]", "do": null }, { "gene_id": 18552, "description": "proprotein convertase subtilisin/kexin type 5", "gene_symbol": "[\"Pcsk5\"]", "do": "[{\"label\":\"VACTERL association\",\"id\":\"DOID:14679\"},{\"label\":\"primary ciliary dyskinesia\",\"id\":\"DOID:9562\"},{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 18553, "description": "proprotein convertase subtilisin/kexin type 6", "gene_symbol": "[\"Pcsk6\"]", "do": null }, { "gene_id": 18554, "description": "proprotein convertase subtilisin/kexin type 7", "gene_symbol": "[\"Pcsk7\"]", "do": null }, { "gene_id": 18566, "description": "programmed cell death 1", "gene_symbol": "[\"Pdcd1\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"},{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 18571, "description": "programmed cell death 6 interacting protein", "gene_symbol": "[\"Pdcd6ip\"]", "do": null }, { "gene_id": 18574, "description": "phosphodiesterase 1B, Ca2+-calmodulin dependent", "gene_symbol": "[\"Pde1b\"]", "do": null }, { "gene_id": 18590, "description": "platelet derived growth factor, alpha", "gene_symbol": "[\"Pdgfa\"]", "do": null }, { "gene_id": 18591, "description": "platelet derived growth factor subunit B", "gene_symbol": "[\"Pdgfb\"]", "do": null }, { "gene_id": 18595, "description": "platelet derived growth factor receptor, alpha polypeptide", "gene_symbol": "[\"Pdgfra\"]", "do": "[{\"label\":\"congenital diaphragmatic hernia\",\"id\":\"DOID:3827\"},{\"label\":\"scimitar syndrome\",\"id\":\"DOID:4297\"}]" }, { "gene_id": 18596, "description": "platelet derived growth factor receptor, beta polypeptide", "gene_symbol": "[\"Pdgfrb\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"basal ganglia calcification\",\"id\":\"DOID:0060230\"},{\"label\":\"infantile myofibromatosis\",\"id\":\"DOID:0080109\"},{\"label\":\"myeloproliferative neoplasm\",\"id\":\"DOID:2226\"},{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"},{\"label\":\"severe nonproliferative diabetic retinopathy\",\"id\":\"DOID:8946\"}]" }, { "gene_id": 18597, "description": "pyruvate dehydrogenase E1 alpha 1", "gene_symbol": "[\"Pdha1\"]", "do": null }, { "gene_id": 18598, "description": "pyruvate dehydrogenase E1 alpha 2", "gene_symbol": "[\"Pdha2\"]", "do": null }, { "gene_id": 18604, "description": "pyruvate dehydrogenase kinase, isoenzyme 2", "gene_symbol": "[\"Pdk2\"]", "do": null }, { "gene_id": 18605, "description": "ectonucleotide pyrophosphatase/phosphodiesterase 1", "gene_symbol": "[\"Enpp1\"]", "do": "[{\"label\":\"arterial calcification of infancy\",\"id\":\"DOID:0050644\"},{\"label\":\"ossification of the posterior longitudinal ligament of spine\",\"id\":\"DOID:0060887\"},{\"label\":\"osteoarthritis\",\"id\":\"DOID:8398\"},{\"label\":\"otitis media\",\"id\":\"DOID:10754\"},{\"label\":\"spondyloarthropathy\",\"id\":\"DOID:1123\"},{\"label\":\"tympanosclerosis\",\"id\":\"DOID:1214\"}]" }, { "gene_id": 18606, "description": "ectonucleotide pyrophosphatase/phosphodiesterase 2", "gene_symbol": "[\"Enpp2\"]", "do": null }, { "gene_id": 18609, "description": "pancreatic and duodenal homeobox 1", "gene_symbol": "[\"Pdx1\"]", "do": "[{\"label\":\"maturity-onset diabetes of the young type 4\",\"id\":\"DOID:0111103\"},{\"label\":\"maturity-onset diabetes of the young\",\"id\":\"DOID:0050524\"},{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 18613, "description": "platelet/endothelial cell adhesion molecule 1", "gene_symbol": "[\"Pecam1\"]", "do": null }, { "gene_id": 18616, "description": "paternally expressed 3", "gene_symbol": "[\"Peg3\"]", "do": null }, { "gene_id": 18619, "description": "preproenkephalin", "gene_symbol": "[\"Penk\"]", "do": null }, { "gene_id": 18626, "description": "period circadian clock 1", "gene_symbol": "[\"Per1\"]", "do": "[{\"label\":\"attention deficit hyperactivity disorder\",\"id\":\"DOID:1094\"}]" }, { "gene_id": 18627, "description": "period circadian clock 2", "gene_symbol": "[\"Per2\"]", "do": "[{\"label\":\"advanced sleep phase syndrome 1\",\"id\":\"DOID:0110011\"}]" }, { "gene_id": 18633, "description": "peroxisomal biogenesis factor 16", "gene_symbol": "[\"Pex16\"]", "do": null }, { "gene_id": 18636, "description": "complement factor properdin", "gene_symbol": "[\"Cfp\"]", "do": null }, { "gene_id": 18637, "description": "prefoldin 2", "gene_symbol": "[\"Pfdn2\"]", "do": null }, { "gene_id": 18639, "description": "6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1", "gene_symbol": "[\"Pfkfb1\"]", "do": null }, { "gene_id": 18640, "description": "6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2", "gene_symbol": "[\"Pfkfb2\"]", "do": null }, { "gene_id": 18641, "description": "phosphofructokinase, liver, B-type", "gene_symbol": "[\"Pfkl\"]", "do": null }, { "gene_id": 18642, "description": "phosphofructokinase, muscle", "gene_symbol": "[\"Pfkm\"]", "do": "[{\"label\":\"glycogen storage disease VII\",\"id\":\"DOID:11721\"}]" }, { "gene_id": 18643, "description": "profilin 1", "gene_symbol": "[\"Pfn1\"]", "do": null }, { "gene_id": 18646, "description": "perforin 1 (pore forming protein)", "gene_symbol": "[\"Prf1\"]", "do": "[{\"label\":\"familial hemophagocytic lymphohistiocytosis 2\",\"id\":\"DOID:0110922\"},{\"label\":\"multiple sclerosis\",\"id\":\"DOID:2377\"},{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 18648, "description": "phosphoglycerate mutase 1", "gene_symbol": "[\"Pgam1\"]", "do": null }, { "gene_id": 18654, "description": "placental growth factor", "gene_symbol": "[\"Pgf\"]", "do": null }, { "gene_id": 18655, "description": "phosphoglycerate kinase 1", "gene_symbol": "[\"Pgk1\"]", "do": null }, { "gene_id": 18663, "description": "phosphoglycerate kinase 2", "gene_symbol": "[\"Pgk2\"]", "do": null }, { "gene_id": 18669, "description": "ATP-binding cassette, sub-family B member 1B", "gene_symbol": "[\"Abcb1b\"]", "do": null }, { "gene_id": 18670, "description": "ATP-binding cassette, sub-family B member 4", "gene_symbol": "[\"Abcb4\"]", "do": "[{\"label\":\"cholecystitis\",\"id\":\"DOID:1949\"},{\"label\":\"cholestasis\",\"id\":\"DOID:13580\"},{\"label\":\"hepatocellular carcinoma\",\"id\":\"DOID:684\"},{\"label\":\"intrahepatic cholestasis\",\"id\":\"DOID:1852\"},{\"label\":\"primary sclerosing cholangitis\",\"id\":\"DOID:0060643\"}]" }, { "gene_id": 18671, "description": "ATP-binding cassette, sub-family B member 1A", "gene_symbol": "[\"Abcb1a\"]", "do": "[{\"label\":\"inflammatory bowel disease 13\",\"id\":\"DOID:0110893\"}]" }, { "gene_id": 18673, "description": "prohibitin 1", "gene_symbol": "[\"Phb1\"]", "do": null }, { "gene_id": 18675, "description": "phosphate regulating endopeptidase homolog, X-linked", "gene_symbol": "[\"Phex\"]", "do": "[{\"label\":\"X-linked hypophosphatemic rickets\",\"id\":\"DOID:0050445\"},{\"label\":\"otitis media\",\"id\":\"DOID:10754\"}]" }, { "gene_id": 18679, "description": "phosphorylase kinase alpha 1", "gene_symbol": "[\"Phka1\"]", "do": "[{\"label\":\"glycogen storage disease IXd\",\"id\":\"DOID:0111040\"}]" }, { "gene_id": 18682, "description": "phosphorylase kinase gamma 1", "gene_symbol": "[\"Phkg1\"]", "do": null }, { "gene_id": 18685, "description": "putative homeodomain transcription factor 1", "gene_symbol": "[\"Phtf1\"]", "do": null }, { "gene_id": 18700, "description": "phosphatidylinositol glycan anchor biosynthesis, class A", "gene_symbol": "[\"Piga\"]", "do": "[{\"label\":\"autosomal recessive congenital ichthyosis 4B\",\"id\":\"DOID:0060713\"}]" }, { "gene_id": 18703, "description": "polymeric immunoglobulin receptor", "gene_symbol": "[\"Pigr\"]", "do": null }, { "gene_id": 18704, "description": "phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha", "gene_symbol": "[\"Pik3c2a\"]", "do": null }, { "gene_id": 18706, "description": "phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha", "gene_symbol": "[\"Pik3ca\"]", "do": "[{\"label\":\"CLOVES syndrome\",\"id\":\"DOID:0080351\"},{\"label\":\"breast cancer\",\"id\":\"DOID:1612\"}]" }, { "gene_id": 18708, "description": "phosphoinositide-3-kinase regulatory subunit 1", "gene_symbol": "[\"Pik3r1\"]", "do": "[{\"label\":\"SHORT syndrome\",\"id\":\"DOID:0111454\"},{\"label\":\"X-linked agammaglobulinemia\",\"id\":\"DOID:14179\"}]" }, { "gene_id": 18717, "description": "phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma", "gene_symbol": "[\"Pip5k1c\"]", "do": null }, { "gene_id": 18718, "description": "phosphatidylinositol-5-phosphate 4-kinase, type II, alpha", "gene_symbol": "[\"Pip4k2a\"]", "do": null }, { "gene_id": 18724, "description": "paired-Ig-like receptor A11", "gene_symbol": "[\"Pira11\"]", "do": null }, { "gene_id": 18727, "description": "paired-Ig-like receptor A4", "gene_symbol": "[\"Pira4\"]", "do": null }, { "gene_id": 18730, "description": "paired-Ig-like receptor A7", "gene_symbol": "[\"Pira7\"]", "do": null }, { "gene_id": 18733, "description": "paired Ig-like receptor B", "gene_symbol": "[\"Pirb\"]", "do": null }, { "gene_id": 18739, "description": "phosphatidylinositol transfer protein, membrane-associated 1", "gene_symbol": "[\"Pitpnm1\"]", "do": null }, { "gene_id": 18746, "description": "pyruvate kinase, muscle", "gene_symbol": "[\"Pkm\"]", "do": null }, { "gene_id": 18751, "description": "protein kinase C, beta", "gene_symbol": "[\"Prkcb\"]", "do": null }, { "gene_id": 18752, "description": "protein kinase C, gamma", "gene_symbol": "[\"Prkcg\"]", "do": "[{\"label\":\"spinocerebellar ataxia 14\",\"id\":\"DOID:0050964\"}]" }, { "gene_id": 18759, "description": "protein kinase C, iota", "gene_symbol": "[\"Prkci\"]", "do": "[{\"label\":\"abdominal obesity-metabolic syndrome\",\"id\":\"DOID:0060611\"},{\"label\":\"obesity\",\"id\":\"DOID:9970\"},{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 18762, "description": "protein kinase C, zeta", "gene_symbol": "[\"Prkcz\"]", "do": null }, { "gene_id": 18763, "description": "polycystin 1, transient receptor potential channel interacting", "gene_symbol": "[\"Pkd1\"]", "do": "[{\"label\":\"autosomal recessive polycystic kidney disease\",\"id\":\"DOID:0110861\"},{\"label\":\"hypertrophic cardiomyopathy\",\"id\":\"DOID:11984\"},{\"label\":\"polycystic kidney disease 1\",\"id\":\"DOID:0110858\"}]" }, { "gene_id": 18764, "description": "polycystin 2, transient receptor potential cation channel", "gene_symbol": "[\"Pkd2\"]", "do": "[{\"label\":\"autosomal dominant polycystic kidney disease\",\"id\":\"DOID:898\"},{\"label\":\"polycystic kidney disease 2\",\"id\":\"DOID:0110859\"}]" }, { "gene_id": 18766, "description": "polycystin (PKD) family receptor for egg jelly", "gene_symbol": "[\"Pkdrej\"]", "do": null }, { "gene_id": 18767, "description": "protein kinase inhibitor, alpha", "gene_symbol": "[\"Pkia\"]", "do": null }, { "gene_id": 18772, "description": "plakophilin 1", "gene_symbol": "[\"Pkp1\"]", "do": null }, { "gene_id": 18777, "description": "lysophospholipase 1", "gene_symbol": "[\"Lypla1\"]", "do": null }, { "gene_id": 18779, "description": "phospholipase A2 receptor 1", "gene_symbol": "[\"Pla2r1\"]", "do": null }, { "gene_id": 18781, "description": "phospholipase A2, group IIC", "gene_symbol": "[\"Pla2g2c\"]", "do": null }, { "gene_id": 18782, "description": "phospholipase A2, group IID", "gene_symbol": "[\"Pla2g2d\"]", "do": null }, { "gene_id": 18783, "description": "phospholipase A2, group IVA (cytosolic, calcium-dependent)", "gene_symbol": "[\"Pla2g4a\"]", "do": null }, { "gene_id": 18788, "description": "serine (or cysteine) peptidase inhibitor, clade B, member 2", "gene_symbol": "[\"Serpinb2\"]", "do": null }, { "gene_id": 18789, "description": "poly (A) polymerase alpha", "gene_symbol": "[\"Papola\"]", "do": null }, { "gene_id": 18791, "description": "plasminogen activator, tissue", "gene_symbol": "[\"Plat\"]", "do": null }, { "gene_id": 18793, "description": "plasminogen activator, urokinase receptor", "gene_symbol": "[\"Plaur\"]", "do": null }, { "gene_id": 18797, "description": "phospholipase C, beta 3", "gene_symbol": "[\"Plcb3\"]", "do": null }, { "gene_id": 18799, "description": "phospholipase C, delta 1", "gene_symbol": "[\"Plcd1\"]", "do": null }, { "gene_id": 18807, "description": "phospholipase D family member 3", "gene_symbol": "[\"Pld3\"]", "do": null }, { "gene_id": 18810, "description": "plectin", "gene_symbol": "[\"Plec\"]", "do": "[{\"label\":\"epidermolysis bullosa simplex 5A Ogna type\",\"id\":\"DOID:0060736\"},{\"label\":\"epidermolysis bullosa simplex with muscular dystrophy\",\"id\":\"DOID:0090017\"}]" }, { "gene_id": 18811, "description": "prolactin family 2, subfamily c, member 2", "gene_symbol": "[\"Prl2c2\"]", "do": null }, { "gene_id": 18812, "description": "prolactin family 2, subfamily c, member 3", "gene_symbol": "[\"Prl2c3\"]", "do": null }, { "gene_id": 18815, "description": "plasminogen", "gene_symbol": "[\"Plg\"]", "do": null }, { "gene_id": 18816, "description": "serine (or cysteine) peptidase inhibitor, clade F, member 2", "gene_symbol": "[\"Serpinf2\"]", "do": "[{\"label\":\"alpha-2-plasmin inhibitor deficiency\",\"id\":\"DOID:0060601\"}]" }, { "gene_id": 18822, "description": "procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1", "gene_symbol": "[\"Plod1\"]", "do": "[{\"label\":\"Ehlers-Danlos syndrome\",\"id\":\"DOID:13359\"}]" }, { "gene_id": 18823, "description": "proteolipid protein (myelin) 1", "gene_symbol": "[\"Plp1\"]", "do": "[{\"label\":\"Pelizaeus-Merzbacher disease\",\"id\":\"DOID:3210\"},{\"label\":\"hereditary spastic paraplegia 2\",\"id\":\"DOID:0110773\"}]" }, { "gene_id": 18830, "description": "phospholipid transfer protein", "gene_symbol": "[\"Pltp\"]", "do": "[{\"label\":\"dry eye syndrome\",\"id\":\"DOID:10140\"}]" }, { "gene_id": 18843, "description": "BPI fold containing family A, member 1", "gene_symbol": "[\"Bpifa1\"]", "do": "[{\"label\":\"otitis media\",\"id\":\"DOID:10754\"}]" }, { "gene_id": 18844, "description": "plexin A1", "gene_symbol": "[\"Plxna1\"]", "do": null }, { "gene_id": 18845, "description": "plexin A2", "gene_symbol": "[\"Plxna2\"]", "do": null }, { "gene_id": 18846, "description": "plexin A3", "gene_symbol": "[\"Plxna3\"]", "do": null }, { "gene_id": 18854, "description": "promyelocytic leukemia", "gene_symbol": "[\"Pml\"]", "do": null }, { "gene_id": 18858, "description": "peripheral myelin protein 22", "gene_symbol": "[\"Pmp22\"]", "do": "[{\"label\":\"Charcot-Marie-Tooth disease type 1A\",\"id\":\"DOID:0110148\"},{\"label\":\"Charcot-Marie-Tooth disease type 1E\",\"id\":\"DOID:0110153\"},{\"label\":\"Charcot-Marie-Tooth disease type 3\",\"id\":\"DOID:0050540\"},{\"label\":\"hereditary neuropathy with liability to pressure palsies\",\"id\":\"DOID:0060843\"}]" }, { "gene_id": 18933, "description": "paired related homeobox 1", "gene_symbol": "[\"Prrx1\"]", "do": null }, { "gene_id": 18946, "description": "pancreatic lipase related protein 1", "gene_symbol": "[\"Pnliprp1\"]", "do": null }, { "gene_id": 18947, "description": "pancreatic lipase-related protein 2", "gene_symbol": "[\"Pnliprp2\"]", "do": null }, { "gene_id": 18950, "description": "purine-nucleoside phosphorylase", "gene_symbol": "[\"Pnp\"]", "do": "[{\"label\":\"purine nucleoside phosphorylase deficiency\",\"id\":\"DOID:5813\"}]" }, { "gene_id": 18951, "description": "septin 5", "gene_symbol": "[\"Septin5\"]", "do": null }, { "gene_id": 18969, "description": "polymerase (DNA directed), alpha 2", "gene_symbol": "[\"Pola2\"]", "do": null }, { "gene_id": 18972, "description": "polymerase (DNA directed), delta 2, regulatory subunit", "gene_symbol": "[\"Pold2\"]", "do": null }, { "gene_id": 18976, "description": "pro-opiomelanocortin-alpha", "gene_symbol": "[\"Pomc\"]", "do": "[{\"label\":\"obesity\",\"id\":\"DOID:9970\"}]" }, { "gene_id": 18979, "description": "paraoxonase 1", "gene_symbol": "[\"Pon1\"]", "do": null }, { "gene_id": 18984, "description": "cytochrome p450 oxidoreductase", "gene_symbol": "[\"Por\"]", "do": null }, { "gene_id": 18986, "description": "POU domain, class 2, transcription factor 1", "gene_symbol": "[\"Pou2f1\"]", "do": null }, { "gene_id": 18999, "description": "POU domain, class 5, transcription factor 1", "gene_symbol": "[\"Pou5f1\"]", "do": null }, { "gene_id": 19012, "description": "phospholipid phosphatase 1", "gene_symbol": "[\"Plpp1\"]", "do": null }, { "gene_id": 19013, "description": "peroxisome proliferator activated receptor alpha", "gene_symbol": "[\"Ppara\"]", "do": "[{\"label\":\"diabetes mellitus\",\"id\":\"DOID:9351\"},{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 19014, "description": "mediator complex subunit 1", "gene_symbol": "[\"Med1\"]", "do": "[{\"label\":\"congestive heart failure\",\"id\":\"DOID:6000\"},{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 19016, "description": "peroxisome proliferator activated receptor gamma", "gene_symbol": "[\"Pparg\"]", "do": "[{\"label\":\"abdominal obesity-metabolic syndrome\",\"id\":\"DOID:0060611\"},{\"label\":\"congenital generalized lipodystrophy type 2\",\"id\":\"DOID:0111136\"},{\"label\":\"familial partial lipodystrophy\",\"id\":\"DOID:0050440\"},{\"label\":\"primary pulmonary hypertension\",\"id\":\"DOID:14557\"},{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 19017, "description": "peroxisome proliferative activated receptor, gamma, coactivator 1 alpha", "gene_symbol": "[\"Ppargc1a\"]", "do": "[{\"label\":\"Parkinson's disease\",\"id\":\"DOID:14330\"},{\"label\":\"age related macular degeneration\",\"id\":\"DOID:10871\"},{\"label\":\"cardiomyopathy\",\"id\":\"DOID:0050700\"},{\"label\":\"congestive heart failure\",\"id\":\"DOID:6000\"}]" }, { "gene_id": 19023, "description": "protein phosphatase, EF hand calcium-binding domain 2", "gene_symbol": "[\"Ppef2\"]", "do": null }, { "gene_id": 19025, "description": "cathepsin A", "gene_symbol": "[\"Ctsa\"]", "do": null }, { "gene_id": 19027, "description": "synaptophysin like 1", "gene_symbol": "[\"Sypl1\"]", "do": null }, { "gene_id": 19035, "description": "peptidylprolyl isomerase B", "gene_symbol": "[\"Ppib\"]", "do": "[{\"label\":\"osteogenesis imperfecta type 9\",\"id\":\"DOID:0110349\"}]" }, { "gene_id": 19039, "description": "lectin, galactoside-binding, soluble, 3 binding protein", "gene_symbol": "[\"Lgals3bp\"]", "do": null }, { "gene_id": 19041, "description": "periplakin", "gene_symbol": "[\"Ppl\"]", "do": null }, { "gene_id": 19045, "description": "protein phosphatase 1 catalytic subunit alpha", "gene_symbol": "[\"Ppp1ca\"]", "do": null }, { "gene_id": 19046, "description": "protein phosphatase 1 catalytic subunit beta", "gene_symbol": "[\"Ppp1cb\"]", "do": null }, { "gene_id": 19047, "description": "protein phosphatase 1 catalytic subunit gamma", "gene_symbol": "[\"Ppp1cc\"]", "do": null }, { "gene_id": 19055, "description": "protein phosphatase 3, catalytic subunit, alpha isoform", "gene_symbol": "[\"Ppp3ca\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 19063, "description": "palmitoyl-protein thioesterase 1", "gene_symbol": "[\"Ppt1\"]", "do": "[{\"label\":\"neuronal ceroid lipofuscinosis 1\",\"id\":\"DOID:0110721\"},{\"label\":\"neuronal ceroid lipofuscinosis 3\",\"id\":\"DOID:0110731\"}]" }, { "gene_id": 19065, "description": "neuropeptide Y receptor Y4", "gene_symbol": "[\"Npy4r\"]", "do": null }, { "gene_id": 19073, "description": "serglycin", "gene_symbol": "[\"Srgn\"]", "do": null }, { "gene_id": 19074, "description": "proteoglycan 2, bone marrow", "gene_symbol": "[\"Prg2\"]", "do": null }, { "gene_id": 19089, "description": "protein kinase C substrate 80K-H", "gene_symbol": "[\"Prkcsh\"]", "do": "[{\"label\":\"polycystic liver disease\",\"id\":\"DOID:0050770\"}]" }, { "gene_id": 19099, "description": "mitogen-activated protein kinase 8 interacting protein 1", "gene_symbol": "[\"Mapk8ip1\"]", "do": null }, { "gene_id": 19110, "description": "prolactin family 4, subfamily a, member 1", "gene_symbol": "[\"Prl4a1\"]", "do": null }, { "gene_id": 19111, "description": "prolactin family 6, subfamily a, member 1", "gene_symbol": "[\"Prl6a1\"]", "do": null }, { "gene_id": 19112, "description": "prolactin family 8, subfamily a, member 6", "gene_symbol": "[\"Prl8a6\"]", "do": null }, { "gene_id": 19113, "description": "prolactin family 7, subfamily a, member 1", "gene_symbol": "[\"Prl7a1\"]", "do": null }, { "gene_id": 19114, "description": "prolactin family 7, subfamily a, member 2", "gene_symbol": "[\"Prl7a2\"]", "do": null }, { "gene_id": 19116, "description": "prolactin receptor", "gene_symbol": "[\"Prlr\"]", "do": "[{\"label\":\"familial medullary thyroid carcinoma\",\"id\":\"DOID:0050547\"}]" }, { "gene_id": 19122, "description": "prion protein", "gene_symbol": "[\"Prnp\"]", "do": "[{\"label\":\"Creutzfeldt-Jakob disease\",\"id\":\"DOID:11949\"},{\"label\":\"Gerstmann-Straussler-Scheinker syndrome\",\"id\":\"DOID:4249\"},{\"label\":\"fatal familial insomnia\",\"id\":\"DOID:0050433\"}]" }, { "gene_id": 19123, "description": "protein C", "gene_symbol": "[\"Proc\"]", "do": null }, { "gene_id": 19124, "description": "protein C receptor, endothelial", "gene_symbol": "[\"Procr\"]", "do": null }, { "gene_id": 19126, "description": "prominin 1", "gene_symbol": "[\"Prom1\"]", "do": "[{\"label\":\"retinitis pigmentosa 41\",\"id\":\"DOID:0110376\"}]" }, { "gene_id": 19128, "description": "protein S (alpha)", "gene_symbol": "[\"Pros1\"]", "do": null }, { "gene_id": 19133, "description": "peripherin 2", "gene_symbol": "[\"Prph2\"]", "do": "[{\"label\":\"partial central choroid dystrophy\",\"id\":\"DOID:9822\"},{\"label\":\"patterned macular dystrophy 1\",\"id\":\"DOID:0060866\"},{\"label\":\"retinitis pigmentosa 7\",\"id\":\"DOID:0110383\"}]" }, { "gene_id": 19139, "description": "phosphoribosyl pyrophosphate synthetase 1", "gene_symbol": "[\"Prps1\"]", "do": null }, { "gene_id": 19141, "description": "legumain", "gene_symbol": "[\"Lgmn\"]", "do": "[{\"label\":\"lymphatic system disease\",\"id\":\"DOID:75\"}]" }, { "gene_id": 19142, "description": "serine protease 12 neurotrypsin (motopsin)", "gene_symbol": "[\"Prss12\"]", "do": null }, { "gene_id": 19143, "description": "suppression of tumorigenicity 14 (colon carcinoma)", "gene_symbol": "[\"St14\"]", "do": "[{\"label\":\"Sjogren's syndrome\",\"id\":\"DOID:12894\"}]" }, { "gene_id": 19146, "description": "transmembrane protease, serine 15", "gene_symbol": "[\"Tmprss15\"]", "do": null }, { "gene_id": 19152, "description": "proteinase 3", "gene_symbol": "[\"Prtn3\"]", "do": null }, { "gene_id": 19156, "description": "prosaposin", "gene_symbol": "[\"Psap\"]", "do": "[{\"label\":\"Krabbe disease\",\"id\":\"DOID:10587\"},{\"label\":\"combined saposin deficiency\",\"id\":\"DOID:0111330\"},{\"label\":\"metachromatic leukodystrophy\",\"id\":\"DOID:10581\"}]" }, { "gene_id": 19167, "description": "proteasome subunit alpha 3", "gene_symbol": "[\"Psma3\"]", "do": null }, { "gene_id": 19170, "description": "proteasome (prosome, macropain) subunit, beta type 1", "gene_symbol": "[\"Psmb1\"]", "do": null }, { "gene_id": 19179, "description": "protease (prosome, macropain) 26S subunit, ATPase 1", "gene_symbol": "[\"Psmc1\"]", "do": null }, { "gene_id": 19181, "description": "proteasome (prosome, macropain) 26S subunit, ATPase 2", "gene_symbol": "[\"Psmc2\"]", "do": null }, { "gene_id": 19184, "description": "protease (prosome, macropain) 26S subunit, ATPase 5", "gene_symbol": "[\"Psmc5\"]", "do": null }, { "gene_id": 19186, "description": "proteasome (prosome, macropain) activator subunit 1 (PA28 alpha)", "gene_symbol": "[\"Psme1\"]", "do": null }, { "gene_id": 19192, "description": "proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki)", "gene_symbol": "[\"Psme3\"]", "do": null }, { "gene_id": 19204, "description": "platelet-activating factor receptor", "gene_symbol": "[\"Ptafr\"]", "do": null }, { "gene_id": 19205, "description": "polypyrimidine tract binding protein 1", "gene_symbol": "[\"Ptbp1\"]", "do": null }, { "gene_id": 19206, "description": "patched 1", "gene_symbol": "[\"Ptch1\"]", "do": "[{\"label\":\"basal cell carcinoma\",\"id\":\"DOID:2513\"},{\"label\":\"medulloblastoma\",\"id\":\"DOID:0050902\"},{\"label\":\"nevoid basal cell carcinoma syndrome\",\"id\":\"DOID:2512\"}]" }, { "gene_id": 19207, "description": "patched 2", "gene_symbol": "[\"Ptch2\"]", "do": null }, { "gene_id": 19208, "description": "pre T cell antigen receptor alpha", "gene_symbol": "[\"Ptcra\"]", "do": null }, { "gene_id": 19214, "description": "prostaglandin D receptor", "gene_symbol": "[\"Ptgdr\"]", "do": null }, { "gene_id": 19215, "description": "prostaglandin D2 synthase (brain)", "gene_symbol": "[\"Ptgds\"]", "do": null }, { "gene_id": 19216, "description": "prostaglandin E receptor 1 (subtype EP1)", "gene_symbol": "[\"Ptger1\"]", "do": null }, { "gene_id": 19217, "description": "prostaglandin E receptor 2 (subtype EP2)", "gene_symbol": "[\"Ptger2\"]", "do": null }, { "gene_id": 19219, "description": "prostaglandin E receptor 4 (subtype EP4)", "gene_symbol": "[\"Ptger4\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 19220, "description": "prostaglandin F receptor", "gene_symbol": "[\"Ptgfr\"]", "do": null }, { "gene_id": 19221, "description": "prostaglandin F2 receptor negative regulator", "gene_symbol": "[\"Ptgfrn\"]", "do": null }, { "gene_id": 19222, "description": "prostaglandin I receptor (IP)", "gene_symbol": "[\"Ptgir\"]", "do": null }, { "gene_id": 19224, "description": "prostaglandin-endoperoxide synthase 1", "gene_symbol": "[\"Ptgs1\"]", "do": "[{\"label\":\"pre-eclampsia\",\"id\":\"DOID:10591\"}]" }, { "gene_id": 19225, "description": "prostaglandin-endoperoxide synthase 2", "gene_symbol": "[\"Ptgs2\"]", "do": null }, { "gene_id": 19228, "description": "parathyroid hormone 1 receptor", "gene_symbol": "[\"Pth1r\"]", "do": null }, { "gene_id": 19231, "description": "prothymosin alpha", "gene_symbol": "[\"Ptma\"]", "do": "[{\"label\":\"polycystic kidney disease\",\"id\":\"DOID:0080322\"},{\"label\":\"pulmonary emphysema\",\"id\":\"DOID:9675\"}]" }, { "gene_id": 19240, "description": "thymosin beta 10", "gene_symbol": "[\"Tmsb10\"]", "do": null }, { "gene_id": 19247, "description": "protein tyrosine phosphatase, non-receptor type 11", "gene_symbol": "[\"Ptpn11\"]", "do": "[{\"label\":\"Noonan syndrome 1\",\"id\":\"DOID:0060578\"},{\"label\":\"Noonan syndrome with multiple lentigines\",\"id\":\"DOID:14291\"},{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"},{\"label\":\"disease of metabolism\",\"id\":\"DOID:0014667\"},{\"label\":\"hepatocellular adenoma\",\"id\":\"DOID:0050868\"},{\"label\":\"hypertrophic cardiomyopathy\",\"id\":\"DOID:11984\"},{\"label\":\"idiopathic scoliosis\",\"id\":\"DOID:0060250\"},{\"label\":\"juvenile myelomonocytic leukemia\",\"id\":\"DOID:0050458\"}]" }, { "gene_id": 19248, "description": "protein tyrosine phosphatase, non-receptor type 12", "gene_symbol": "[\"Ptpn12\"]", "do": null }, { "gene_id": 19249, "description": "protein tyrosine phosphatase, non-receptor type 13", "gene_symbol": "[\"Ptpn13\"]", "do": null }, { "gene_id": 19250, "description": "protein tyrosine phosphatase, non-receptor type 14", "gene_symbol": "[\"Ptpn14\"]", "do": null }, { "gene_id": 19255, "description": "protein tyrosine phosphatase, non-receptor type 2", "gene_symbol": "[\"Ptpn2\"]", "do": null }, { "gene_id": 19259, "description": "protein tyrosine phosphatase, non-receptor type 5", "gene_symbol": "[\"Ptpn5\"]", "do": null }, { "gene_id": 19261, "description": "signal-regulatory protein alpha", "gene_symbol": "[\"Sirpa\"]", "do": null }, { "gene_id": 19262, "description": "protein tyrosine phosphatase receptor type A", "gene_symbol": "[\"Ptpra\"]", "do": null }, { "gene_id": 19263, "description": "protein tyrosine phosphatase receptor type B", "gene_symbol": "[\"Ptprb\"]", "do": null }, { "gene_id": 19264, "description": "protein tyrosine phosphatase receptor type C", "gene_symbol": "[\"Ptprc\"]", "do": "[{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 19266, "description": "protein tyrosine phosphatase receptor type D", "gene_symbol": "[\"Ptprd\"]", "do": null }, { "gene_id": 19267, "description": "protein tyrosine phosphatase receptor type E", "gene_symbol": "[\"Ptpre\"]", "do": null }, { "gene_id": 19268, "description": "protein tyrosine phosphatase receptor type F", "gene_symbol": "[\"Ptprf\"]", "do": null }, { "gene_id": 19270, "description": "protein tyrosine phosphatase receptor type G", "gene_symbol": "[\"Ptprg\"]", "do": null }, { "gene_id": 19271, "description": "protein tyrosine phosphatase receptor type J", "gene_symbol": "[\"Ptprj\"]", "do": null }, { "gene_id": 19272, "description": "protein tyrosine phosphatase receptor type K", "gene_symbol": "[\"Ptprk\"]", "do": null }, { "gene_id": 19273, "description": "protein tyrosine phosphatase receptor type U", "gene_symbol": "[\"Ptpru\"]", "do": null }, { "gene_id": 19274, "description": "protein tyrosine phosphatase receptor type M", "gene_symbol": "[\"Ptprm\"]", "do": null }, { "gene_id": 19276, "description": "protein tyrosine phosphatase receptor type N polypeptide 2", "gene_symbol": "[\"Ptprn2\"]", "do": "[{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 19277, "description": "protein tyrosine phosphatase receptor type O", "gene_symbol": "[\"Ptpro\"]", "do": null }, { "gene_id": 19279, "description": "protein tyrosine phosphatase receptor type R", "gene_symbol": "[\"Ptprr\"]", "do": null }, { "gene_id": 19280, "description": "protein tyrosine phosphatase receptor type S", "gene_symbol": "[\"Ptprs\"]", "do": null }, { "gene_id": 19281, "description": "protein tyrosine phosphatase receptor type T", "gene_symbol": "[\"Ptprt\"]", "do": null }, { "gene_id": 19283, "description": "protein tyrosine phosphatase receptor type Z, polypeptide 1", "gene_symbol": "[\"Ptprz1\"]", "do": null }, { "gene_id": 19285, "description": "caveolae associated 1", "gene_symbol": "[\"Cavin1\"]", "do": "[{\"label\":\"congenital generalized lipodystrophy type 4\",\"id\":\"DOID:0111138\"},{\"label\":\"pulmonary hypertension\",\"id\":\"DOID:6432\"}]" }, { "gene_id": 19288, "description": "pentraxin related gene", "gene_symbol": "[\"Ptx3\"]", "do": null }, { "gene_id": 19289, "description": "immunoglobulin superfamily, DCC subclass, member 3", "gene_symbol": "[\"Igdcc3\"]", "do": null }, { "gene_id": 19290, "description": "purine rich element binding protein A", "gene_symbol": "[\"Pura\"]", "do": null }, { "gene_id": 19294, "description": "nectin cell adhesion molecule 2", "gene_symbol": "[\"Nectin2\"]", "do": null }, { "gene_id": 19299, "description": "ATP-binding cassette, sub-family D member 3", "gene_symbol": "[\"Abcd3\"]", "do": "[{\"label\":\"congenital bile acid synthesis defect 5\",\"id\":\"DOID:0111066\"}]" }, { "gene_id": 19303, "description": "paxillin", "gene_symbol": "[\"Pxn\"]", "do": null }, { "gene_id": 19305, "description": "peroxisomal biogenesis factor 5", "gene_symbol": "[\"Pex5\"]", "do": null }, { "gene_id": 19309, "description": "muscle glycogen phosphorylase", "gene_symbol": "[\"Pygm\"]", "do": "[{\"label\":\"glycogen storage disease V\",\"id\":\"DOID:2746\"}]" }, { "gene_id": 19317, "description": "quaking, KH domain containing RNA binding", "gene_symbol": "[\"Qki\"]", "do": null }, { "gene_id": 19334, "description": "RAB22A, member RAS oncogene family", "gene_symbol": "[\"Rab22a\"]", "do": null }, { "gene_id": 19335, "description": "RAB23, member RAS oncogene family", "gene_symbol": "[\"Rab23\"]", "do": null }, { "gene_id": 19339, "description": "RAB3A, member RAS oncogene family", "gene_symbol": "[\"Rab3a\"]", "do": null }, { "gene_id": 19342, "description": "RAB4B, member RAS oncogene family", "gene_symbol": "[\"Rab4b\"]", "do": null }, { "gene_id": 19346, "description": "RAB6A, member RAS oncogene family", "gene_symbol": "[\"Rab6a\"]", "do": null }, { "gene_id": 19355, "description": "RAD1 checkpoint DNA exonuclease", "gene_symbol": "[\"Rad1\"]", "do": null }, { "gene_id": 19358, "description": "RAD23 homolog A, nucleotide excision repair protein", "gene_symbol": "[\"Rad23a\"]", "do": null }, { "gene_id": 19359, "description": "RAD23 homolog B, nucleotide excision repair protein", "gene_symbol": "[\"Rad23b\"]", "do": null }, { "gene_id": 19365, "description": "RAD52 homolog, DNA repair protein", "gene_symbol": "[\"Rad52\"]", "do": null }, { "gene_id": 19368, "description": "retinoic acid early transcript 1, alpha", "gene_symbol": "[\"Raet1a\"]", "do": null }, { "gene_id": 19369, "description": "retinoic acid early transcript beta", "gene_symbol": "[\"Raet1b\"]", "do": null }, { "gene_id": 19370, "description": "retinoic acid early transcript gamma", "gene_symbol": "[\"Raet1c\"]", "do": null }, { "gene_id": 19377, "description": "retinoic acid induced 1", "gene_symbol": "[\"Rai1\"]", "do": "[{\"label\":\"Potocki-Lupski syndrome\",\"id\":\"DOID:0060853\"},{\"label\":\"Smith-Magenis syndrome\",\"id\":\"DOID:0060768\"}]" }, { "gene_id": 19384, "description": "RAN, member RAS oncogene family", "gene_symbol": "[\"Ran\"]", "do": null }, { "gene_id": 19386, "description": "RAN binding protein 2", "gene_symbol": "[\"Ranbp2\"]", "do": null }, { "gene_id": 19387, "description": "RAN GTPase activating protein 1", "gene_symbol": "[\"Rangap1\"]", "do": null }, { "gene_id": 19414, "description": "RAS p21 protein activator 3", "gene_symbol": "[\"Rasa3\"]", "do": "[{\"label\":\"aplastic anemia\",\"id\":\"DOID:12449\"}]" }, { "gene_id": 19417, "description": "RAS protein-specific guanine nucleotide-releasing factor 1", "gene_symbol": "[\"Rasgrf1\"]", "do": null }, { "gene_id": 19418, "description": "RAS protein-specific guanine nucleotide-releasing factor 2", "gene_symbol": "[\"Rasgrf2\"]", "do": null }, { "gene_id": 19428, "description": "RAS-like, family 2, locus 9", "gene_symbol": "[\"Rasl2-9\"]", "do": null }, { "gene_id": 19646, "description": "retinoblastoma binding protein 4, chromatin remodeling factor", "gene_symbol": "[\"Rbbp4\"]", "do": null }, { "gene_id": 19647, "description": "retinoblastoma binding protein 6, ubiquitin ligase", "gene_symbol": "[\"Rbbp6\"]", "do": null }, { "gene_id": 19649, "description": "roundabout guidance receptor 3", "gene_symbol": "[\"Robo3\"]", "do": null }, { "gene_id": 19650, "description": "RB transcriptional corepressor like 1", "gene_symbol": "[\"Rbl1\"]", "do": null }, { "gene_id": 19651, "description": "RB transcriptional corepressor like 2", "gene_symbol": "[\"Rbl2\"]", "do": null }, { "gene_id": 19655, "description": "RNA binding motif protein, X chromosome", "gene_symbol": "[\"Rbmx\"]", "do": null }, { "gene_id": 19661, "description": "retinol binding protein 3, interstitial", "gene_symbol": "[\"Rbp3\"]", "do": null }, { "gene_id": 19662, "description": "retinol binding protein 4, plasma", "gene_symbol": "[\"Rbp4\"]", "do": null }, { "gene_id": 19672, "description": "reticulocalbin 1", "gene_symbol": "[\"Rcn1\"]", "do": null }, { "gene_id": 19692, "description": "regenerating islet-derived 1", "gene_symbol": "[\"Reg1\"]", "do": null }, { "gene_id": 19697, "description": "Rela proto-oncogene, NFKB subunit", "gene_symbol": "[\"Rela\"]", "do": null }, { "gene_id": 19699, "description": "reelin", "gene_symbol": "[\"Reln\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 19701, "description": "renin 1 structural", "gene_symbol": "[\"Ren1\"]", "do": null }, { "gene_id": 19703, "description": "renin binding protein", "gene_symbol": "[\"Renbp\"]", "do": null }, { "gene_id": 19704, "description": "UPF1 RNA helicase and ATPase", "gene_symbol": "[\"Upf1\"]", "do": null }, { "gene_id": 19707, "description": "RalBP1 associated Eps domain containing protein", "gene_symbol": "[\"Reps1\"]", "do": null }, { "gene_id": 19712, "description": "RE1-silencing transcription factor", "gene_symbol": "[\"Rest\"]", "do": null }, { "gene_id": 19713, "description": "ret proto-oncogene", "gene_symbol": "[\"Ret\"]", "do": "[{\"label\":\"Hirschsprung's disease\",\"id\":\"DOID:10487\"},{\"label\":\"clubfoot\",\"id\":\"DOID:11836\"},{\"label\":\"multiple endocrine neoplasia type 2B\",\"id\":\"DOID:10016\"},{\"label\":\"pheochromocytoma\",\"id\":\"DOID:0050771\"}]" }, { "gene_id": 19719, "description": "RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase", "gene_symbol": "[\"Rfng\"]", "do": null }, { "gene_id": 19724, "description": "regulatory factor X, 1 (influences HLA class II expression)", "gene_symbol": "[\"Rfx1\"]", "do": null }, { "gene_id": 19733, "description": "regucalcin", "gene_symbol": "[\"Rgn\"]", "do": null }, { "gene_id": 19743, "description": "Rhesus blood group-associated A glycoprotein", "gene_symbol": "[\"Rhag\"]", "do": null }, { "gene_id": 19746, "description": "Rh blood group, D antigen", "gene_symbol": "[\"Rhd\"]", "do": null }, { "gene_id": 19752, "description": "ribonuclease, RNase A family, 1 (pancreatic)", "gene_symbol": "[\"Rnase1\"]", "do": null }, { "gene_id": 19876, "description": "roundabout guidance receptor 1", "gene_symbol": "[\"Robo1\"]", "do": "[{\"label\":\"cystic kidney disease\",\"id\":\"DOID:2975\"},{\"label\":\"lung cancer\",\"id\":\"DOID:1324\"}]" }, { "gene_id": 19877, "description": "Rho-associated coiled-coil containing protein kinase 1", "gene_symbol": "[\"Rock1\"]", "do": null }, { "gene_id": 19878, "description": "Rho-associated coiled-coil containing protein kinase 2", "gene_symbol": "[\"Rock2\"]", "do": null }, { "gene_id": 19879, "description": "solute carrier family 22 (organic anion transporter), member 8", "gene_symbol": "[\"Slc22a8\"]", "do": null }, { "gene_id": 19882, "description": "macrophage stimulating 1 receptor (c-met-related tyrosine kinase)", "gene_symbol": "[\"Mst1r\"]", "do": null }, { "gene_id": 19885, "description": "RAR-related orphan receptor gamma", "gene_symbol": "[\"Rorc\"]", "do": null }, { "gene_id": 19886, "description": "Ros1 proto-oncogene, receptor tyrosine kinase", "gene_symbol": "[\"Ros1\"]", "do": null }, { "gene_id": 19893, "description": "retinitis pigmentosa GTPase regulator", "gene_symbol": "[\"Rpgr\"]", "do": "[{\"label\":\"X-linked cone-rod dystrophy 1\",\"id\":\"DOID:0111008\"},{\"label\":\"retinitis pigmentosa 3\",\"id\":\"DOID:0110414\"}]" }, { "gene_id": 19894, "description": "rabphilin 3A", "gene_symbol": "[\"Rph3a\"]", "do": null }, { "gene_id": 19895, "description": "ribose 5-phosphate isomerase A", "gene_symbol": "[\"Rpia\"]", "do": null }, { "gene_id": 19921, "description": "ribosomal protein L19", "gene_symbol": "[\"Rpl19\"]", "do": null }, { "gene_id": 19941, "description": "ribosomal protein L26", "gene_symbol": "[\"Rpl26\"]", "do": null }, { "gene_id": 19944, "description": "ribosomal protein L29", "gene_symbol": "[\"Rpl29\"]", "do": null }, { "gene_id": 19951, "description": "ribosomal protein L32", "gene_symbol": "[\"Rpl32\"]", "do": null }, { "gene_id": 19988, "description": "ribosomal protein L6", "gene_symbol": "[\"Rpl6\"]", "do": null }, { "gene_id": 20014, "description": "ribophorin II", "gene_symbol": "[\"Rpn2\"]", "do": null }, { "gene_id": 20020, "description": "polymerase (RNA) II (DNA directed) polypeptide A", "gene_symbol": "[\"Polr2a\"]", "do": null }, { "gene_id": 20044, "description": "ribosomal protein S14", "gene_symbol": "[\"Rps14\"]", "do": null }, { "gene_id": 20102, "description": "ribosomal protein S4, X-linked", "gene_symbol": "[\"Rps4x\"]", "do": null }, { "gene_id": 20103, "description": "ribosomal protein S5", "gene_symbol": "[\"Rps5\"]", "do": null }, { "gene_id": 20104, "description": "ribosomal protein S6", "gene_symbol": "[\"Rps6\"]", "do": null }, { "gene_id": 20111, "description": "ribosomal protein S6 kinase A1", "gene_symbol": "[\"Rps6ka1\"]", "do": null }, { "gene_id": 20129, "description": "repetin", "gene_symbol": "[\"Rptn\"]", "do": null }, { "gene_id": 20132, "description": "retinal pigment epithelium derived rhodopsin homolog", "gene_symbol": "[\"Rrh\"]", "do": null }, { "gene_id": 20133, "description": "ribonucleotide reductase M1", "gene_symbol": "[\"Rrm1\"]", "do": null }, { "gene_id": 20168, "description": "reticulon 3", "gene_symbol": "[\"Rtn3\"]", "do": "[{\"label\":\"chronic kidney disease\",\"id\":\"DOID:784\"}]" }, { "gene_id": 20181, "description": "retinoid X receptor alpha", "gene_symbol": "[\"Rxra\"]", "do": "[{\"label\":\"congenital heart disease\",\"id\":\"DOID:1682\"},{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"},{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 20182, "description": "retinoid X receptor beta", "gene_symbol": "[\"Rxrb\"]", "do": null }, { "gene_id": 20183, "description": "retinoid X receptor gamma", "gene_symbol": "[\"Rxrg\"]", "do": null }, { "gene_id": 20184, "description": "ubiquitin interaction motif containing 1", "gene_symbol": "[\"Uimc1\"]", "do": null }, { "gene_id": 20187, "description": "receptor-like tyrosine kinase", "gene_symbol": "[\"Ryk\"]", "do": null }, { "gene_id": 20190, "description": "ryanodine receptor 1, skeletal muscle", "gene_symbol": "[\"Ryr1\"]", "do": "[{\"label\":\"congenital myopathy 1A\",\"id\":\"DOID:3529\"},{\"label\":\"congenital myopathy 1B\",\"id\":\"DOID:0080991\"},{\"label\":\"malignant hyperthermia\",\"id\":\"DOID:8545\"}]" }, { "gene_id": 20191, "description": "ryanodine receptor 2, cardiac", "gene_symbol": "[\"Ryr2\"]", "do": "[{\"label\":\"catecholaminergic polymorphic ventricular tachycardia 1\",\"id\":\"DOID:0060675\"},{\"label\":\"heart disease\",\"id\":\"DOID:114\"}]" }, { "gene_id": 20218, "description": "KH domain containing, RNA binding, signal transduction associated 1", "gene_symbol": "[\"Khdrbs1\"]", "do": null }, { "gene_id": 20219, "description": "amyloid P component, serum", "gene_symbol": "[\"Apcs\"]", "do": null }, { "gene_id": 20226, "description": "seryl-tRNA synthetase 1", "gene_symbol": "[\"Sars1\"]", "do": null }, { "gene_id": 20234, "description": "spermine binding protein", "gene_symbol": "[\"Sbp\"]", "do": null }, { "gene_id": 20238, "description": "ataxin 1", "gene_symbol": "[\"Atxn1\"]", "do": "[{\"label\":\"spinocerebellar ataxia 1\",\"id\":\"DOID:0050954\"}]" }, { "gene_id": 20239, "description": "ataxin 2", "gene_symbol": "[\"Atxn2\"]", "do": "[{\"label\":\"spinocerebellar ataxia 2\",\"id\":\"DOID:0050955\"}]" }, { "gene_id": 20255, "description": "secretogranin III", "gene_symbol": "[\"Scg3\"]", "do": null }, { "gene_id": 20264, "description": "sodium channel, voltage-gated, type X, alpha", "gene_symbol": "[\"Scn10a\"]", "do": null }, { "gene_id": 20265, "description": "sodium channel, voltage-gated, type I, alpha", "gene_symbol": "[\"Scn1a\"]", "do": "[{\"label\":\"Dravet syndrome\",\"id\":\"DOID:0080422\"},{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"generalized epilepsy with febrile seizures plus\",\"id\":\"DOID:0060170\"}]" }, { "gene_id": 20266, "description": "sodium channel, voltage-gated, type I, beta", "gene_symbol": "[\"Scn1b\"]", "do": "[{\"label\":\"generalized epilepsy with febrile seizures plus\",\"id\":\"DOID:0060170\"}]" }, { "gene_id": 20269, "description": "sodium channel, voltage-gated, type III, alpha", "gene_symbol": "[\"Scn3a\"]", "do": null }, { "gene_id": 20271, "description": "sodium channel, voltage-gated, type V, alpha", "gene_symbol": "[\"Scn5a\"]", "do": "[{\"label\":\"Brugada syndrome 1\",\"id\":\"DOID:0110218\"},{\"label\":\"long QT syndrome 3\",\"id\":\"DOID:0110646\"},{\"label\":\"progressive familial heart block type IA\",\"id\":\"DOID:0111074\"},{\"label\":\"sick sinus syndrome\",\"id\":\"DOID:13884\"}]" }, { "gene_id": 20272, "description": "sodium channel, voltage-gated, type VII, alpha", "gene_symbol": "[\"Scn7a\"]", "do": null }, { "gene_id": 20273, "description": "sodium channel, voltage-gated, type VIII, alpha", "gene_symbol": "[\"Scn8a\"]", "do": "[{\"label\":\"early infantile epileptic encephalopathy\",\"id\":\"DOID:0050709\"},{\"label\":\"epilepsy\",\"id\":\"DOID:1826\"}]" }, { "gene_id": 20276, "description": "sodium channel, nonvoltage-gated 1 alpha", "gene_symbol": "[\"Scnn1a\"]", "do": null }, { "gene_id": 20277, "description": "sodium channel, nonvoltage-gated 1 beta", "gene_symbol": "[\"Scnn1b\"]", "do": "[{\"label\":\"Liddle syndrome\",\"id\":\"DOID:0050477\"},{\"label\":\"autosomal recessive pseudohypoaldosteronism type 1\",\"id\":\"DOID:0060854\"},{\"label\":\"cystic fibrosis\",\"id\":\"DOID:1485\"}]" }, { "gene_id": 20278, "description": "sodium channel, nonvoltage-gated 1 gamma", "gene_symbol": "[\"Scnn1g\"]", "do": "[{\"label\":\"autosomal recessive pseudohypoaldosteronism type 1\",\"id\":\"DOID:0060854\"}]" }, { "gene_id": 20280, "description": "sterol carrier protein 2, liver", "gene_symbol": "[\"Scp2\"]", "do": null }, { "gene_id": 20284, "description": "scrapie responsive gene 1", "gene_symbol": "[\"Scrg1\"]", "do": null }, { "gene_id": 20288, "description": "macrophage scavenger receptor 1", "gene_symbol": "[\"Msr1\"]", "do": null }, { "gene_id": 20290, "description": "C-C motif chemokine ligand 1", "gene_symbol": "[\"Ccl1\"]", "do": null }, { "gene_id": 20292, "description": "C-C motif chemokine ligand 11", "gene_symbol": "[\"Ccl11\"]", "do": null }, { "gene_id": 20296, "description": "C-C motif chemokine ligand 2", "gene_symbol": "[\"Ccl2\"]", "do": "[{\"label\":\"age related macular degeneration\",\"id\":\"DOID:10871\"}]" }, { "gene_id": 20306, "description": "C-C motif chemokine ligand 7", "gene_symbol": "[\"Ccl7\"]", "do": null }, { "gene_id": 20317, "description": "serine (or cysteine) peptidase inhibitor, clade F, member 1", "gene_symbol": "[\"Serpinf1\"]", "do": "[{\"label\":\"osteogenesis imperfecta type 6\",\"id\":\"DOID:0110350\"}]" }, { "gene_id": 20318, "description": "stromal cell derived factor 4", "gene_symbol": "[\"Sdf4\"]", "do": null }, { "gene_id": 20320, "description": "neuroplastin", "gene_symbol": "[\"Nptn\"]", "do": null }, { "gene_id": 20321, "description": "ferric-chelate reductase 1", "gene_symbol": "[\"Frrs1\"]", "do": null }, { "gene_id": 20322, "description": "sorbitol dehydrogenase", "gene_symbol": "[\"Sord\"]", "do": "[{\"label\":\"cataract\",\"id\":\"DOID:83\"}]" }, { "gene_id": 20333, "description": "SEC22 homolog B, vesicle trafficking protein", "gene_symbol": "[\"Sec22b\"]", "do": null }, { "gene_id": 20334, "description": "SEC23 homolog A, COPII coat complex component", "gene_symbol": "[\"Sec23a\"]", "do": null }, { "gene_id": 20338, "description": "sel-1 suppressor of lin-12-like (C. elegans)", "gene_symbol": "[\"Sel1l\"]", "do": null }, { "gene_id": 20339, "description": "selectin, endothelial cell", "gene_symbol": "[\"Sele\"]", "do": null }, { "gene_id": 20340, "description": "golgi apparatus protein 1", "gene_symbol": "[\"Glg1\"]", "do": null }, { "gene_id": 20341, "description": "selenium binding protein 1", "gene_symbol": "[\"Selenbp1\"]", "do": null }, { "gene_id": 20342, "description": "selenium binding protein 2", "gene_symbol": "[\"Selenbp2\"]", "do": null }, { "gene_id": 20343, "description": "selectin, lymphocyte", "gene_symbol": "[\"Sell\"]", "do": "[{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 20344, "description": "selectin, platelet", "gene_symbol": "[\"Selp\"]", "do": null }, { "gene_id": 20346, "description": "sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A", "gene_symbol": "[\"Sema3a\"]", "do": null }, { "gene_id": 20348, "description": "sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C", "gene_symbol": "[\"Sema3c\"]", "do": null }, { "gene_id": 20349, "description": "sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E", "gene_symbol": "[\"Sema3e\"]", "do": null }, { "gene_id": 20350, "description": "sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F", "gene_symbol": "[\"Sema3f\"]", "do": null }, { "gene_id": 20351, "description": "sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A", "gene_symbol": "[\"Sema4a\"]", "do": null }, { "gene_id": 20352, "description": "sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B", "gene_symbol": "[\"Sema4b\"]", "do": null }, { "gene_id": 20353, "description": "sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C", "gene_symbol": "[\"Sema4c\"]", "do": null }, { "gene_id": 20354, "description": "sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D", "gene_symbol": "[\"Sema4d\"]", "do": null }, { "gene_id": 20355, "description": "sema domain, immunoglobulin domain (Ig), TM domain, and short cytoplasmic domain", "gene_symbol": "[\"Sema4f\"]", "do": null }, { "gene_id": 20357, "description": "sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B", "gene_symbol": "[\"Sema5b\"]", "do": null }, { "gene_id": 20358, "description": "sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A", "gene_symbol": "[\"Sema6a\"]", "do": null }, { "gene_id": 20359, "description": "sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6B", "gene_symbol": "[\"Sema6b\"]", "do": null }, { "gene_id": 20360, "description": "sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C", "gene_symbol": "[\"Sema6c\"]", "do": null }, { "gene_id": 20361, "description": "sema domain, immunoglobulin domain (Ig), and GPI membrane anchor, (semaphorin) 7A", "gene_symbol": "[\"Sema7a\"]", "do": null }, { "gene_id": 20363, "description": "selenoprotein P", "gene_symbol": "[\"Selenop\"]", "do": null }, { "gene_id": 20370, "description": "seizure related gene 6", "gene_symbol": "[\"Sez6\"]", "do": null }, { "gene_id": 20371, "description": "forkhead box P3", "gene_symbol": "[\"Foxp3\"]", "do": "[{\"label\":\"Wiskott-Aldrich syndrome\",\"id\":\"DOID:9169\"},{\"label\":\"immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome\",\"id\":\"DOID:0090110\"}]" }, { "gene_id": 20377, "description": "secreted frizzled-related protein 1", "gene_symbol": "[\"Sfrp1\"]", "do": null }, { "gene_id": 20378, "description": "frizzled-related protein", "gene_symbol": "[\"Frzb\"]", "do": null }, { "gene_id": 20379, "description": "secreted frizzled-related protein 4", "gene_symbol": "[\"Sfrp4\"]", "do": null }, { "gene_id": 20383, "description": "serine and arginine-rich splicing factor 3", "gene_symbol": "[\"Srsf3\"]", "do": null }, { "gene_id": 20388, "description": "surfactant associated protein B", "gene_symbol": "[\"Sftpb\"]", "do": null }, { "gene_id": 20390, "description": "surfactant associated protein D", "gene_symbol": "[\"Sftpd\"]", "do": null }, { "gene_id": 20391, "description": "sarcoglycan, alpha (dystrophin-associated glycoprotein)", "gene_symbol": "[\"Sgca\"]", "do": "[{\"label\":\"autosomal recessive limb-girdle muscular dystrophy type 2D\",\"id\":\"DOID:0110278\"}]" }, { "gene_id": 20392, "description": "sarcoglycan, epsilon", "gene_symbol": "[\"Sgce\"]", "do": "[{\"label\":\"myoclonic dystonia 11\",\"id\":\"DOID:0090034\"}]" }, { "gene_id": 20401, "description": "SH3-domain binding protein 1", "gene_symbol": "[\"Sh3bp1\"]", "do": null }, { "gene_id": 20405, "description": "SH3-domain GRB2-like 1", "gene_symbol": "[\"Sh3gl1\"]", "do": null }, { "gene_id": 20410, "description": "sorbin and SH3 domain containing 3", "gene_symbol": "[\"Sorbs3\"]", "do": null }, { "gene_id": 20411, "description": "sorbin and SH3 domain containing 1", "gene_symbol": "[\"Sorbs1\"]", "do": null }, { "gene_id": 20415, "description": "sex hormone binding globulin", "gene_symbol": "[\"Shbg\"]", "do": null }, { "gene_id": 20423, "description": "sonic hedgehog", "gene_symbol": "[\"Shh\"]", "do": "[{\"label\":\"holoprosencephaly 3\",\"id\":\"DOID:0110875\"},{\"label\":\"nevoid basal cell carcinoma syndrome\",\"id\":\"DOID:2512\"}]" }, { "gene_id": 20425, "description": "serine hydroxymethyltransferase 1 (soluble)", "gene_symbol": "[\"Shmt1\"]", "do": null }, { "gene_id": 20431, "description": "premelanosome protein", "gene_symbol": "[\"Pmel\"]", "do": null }, { "gene_id": 20440, "description": "beta galactoside alpha 2,6 sialyltransferase 1", "gene_symbol": "[\"St6gal1\"]", "do": null }, { "gene_id": 20441, "description": "ST3 beta-galactoside alpha-2,3-sialyltransferase 3", "gene_symbol": "[\"St3gal3\"]", "do": null }, { "gene_id": 20442, "description": "ST3 beta-galactoside alpha-2,3-sialyltransferase 1", "gene_symbol": "[\"St3gal1\"]", "do": null }, { "gene_id": 20443, "description": "ST3 beta-galactoside alpha-2,3-sialyltransferase 4", "gene_symbol": "[\"St3gal4\"]", "do": null }, { "gene_id": 20444, "description": "ST3 beta-galactoside alpha-2,3-sialyltransferase 2", "gene_symbol": "[\"St3gal2\"]", "do": null }, { "gene_id": 20445, "description": "ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1", "gene_symbol": "[\"St6galnac1\"]", "do": "[{\"label\":\"inflammatory bowel disease\",\"id\":\"DOID:0050589\"}]" }, { "gene_id": 20446, "description": "ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2", "gene_symbol": "[\"St6galnac2\"]", "do": null }, { "gene_id": 20447, "description": "ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3", "gene_symbol": "[\"St6galnac3\"]", "do": null }, { "gene_id": 20448, "description": "ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 4", "gene_symbol": "[\"St6galnac4\"]", "do": null }, { "gene_id": 20449, "description": "ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1", "gene_symbol": "[\"St8sia1\"]", "do": null }, { "gene_id": 20450, "description": "ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2", "gene_symbol": "[\"St8sia2\"]", "do": null }, { "gene_id": 20451, "description": "ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3", "gene_symbol": "[\"St8sia3\"]", "do": null }, { "gene_id": 20452, "description": "ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4", "gene_symbol": "[\"St8sia4\"]", "do": null }, { "gene_id": 20454, "description": "ST3 beta-galactoside alpha-2,3-sialyltransferase 5", "gene_symbol": "[\"St3gal5\"]", "do": null }, { "gene_id": 20466, "description": "SIN3 transcription regulator family member A", "gene_symbol": "[\"Sin3a\"]", "do": null }, { "gene_id": 20474, "description": "sine oculis-related homeobox 4", "gene_symbol": "[\"Six4\"]", "do": null }, { "gene_id": 20482, "description": "SKI-like proto-oncogene", "gene_symbol": "[\"Skil\"]", "do": null }, { "gene_id": 20493, "description": "solute carrier family 10 (sodium/bile acid cotransporter family), member 1", "gene_symbol": "[\"Slc10a1\"]", "do": null }, { "gene_id": 20494, "description": "solute carrier family 10, member 2", "gene_symbol": "[\"Slc10a2\"]", "do": null }, { "gene_id": 20495, "description": "solute carrier family 12, member 1", "gene_symbol": "[\"Slc12a1\"]", "do": "[{\"label\":\"Bartter disease type 1\",\"id\":\"DOID:0110142\"}]" }, { "gene_id": 20496, "description": "solute carrier family 12, member 2", "gene_symbol": "[\"Slc12a2\"]", "do": null }, { "gene_id": 20497, "description": "solute carrier family 12, member 3", "gene_symbol": "[\"Slc12a3\"]", "do": "[{\"label\":\"Gitelman syndrome\",\"id\":\"DOID:0050450\"}]" }, { "gene_id": 20498, "description": "solute carrier family 12, member 4", "gene_symbol": "[\"Slc12a4\"]", "do": null }, { "gene_id": 20499, "description": "solute carrier family 12, member 7", "gene_symbol": "[\"Slc12a7\"]", "do": null }, { "gene_id": 20504, "description": "solute carrier family 17 (sodium phosphate), member 1", "gene_symbol": "[\"Slc17a1\"]", "do": null }, { "gene_id": 20505, "description": "solute carrier family 34 (sodium phosphate), member 1", "gene_symbol": "[\"Slc34a1\"]", "do": "[{\"label\":\"hereditary hypophosphatemic rickets with hypercalciuria\",\"id\":\"DOID:0050947\"}]" }, { "gene_id": 20510, "description": "solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1", "gene_symbol": "[\"Slc1a1\"]", "do": "[{\"label\":\"dicarboxylic aminoaciduria\",\"id\":\"DOID:0060650\"},{\"label\":\"low tension glaucoma\",\"id\":\"DOID:13544\"}]" }, { "gene_id": 20511, "description": "solute carrier family 1 (glial high affinity glutamate transporter), member 2", "gene_symbol": "[\"Slc1a2\"]", "do": null }, { "gene_id": 20512, "description": "solute carrier family 1 (glial high affinity glutamate transporter), member 3", "gene_symbol": "[\"Slc1a3\"]", "do": "[{\"label\":\"low tension glaucoma\",\"id\":\"DOID:13544\"}]" }, { "gene_id": 20513, "description": "solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6", "gene_symbol": "[\"Slc1a6\"]", "do": null }, { "gene_id": 20516, "description": "solute carrier family 20, member 2", "gene_symbol": "[\"Slc20a2\"]", "do": "[{\"label\":\"basal ganglia calcification\",\"id\":\"DOID:0060230\"}]" }, { "gene_id": 20517, "description": "solute carrier family 22 (organic cation transporter), member 1", "gene_symbol": "[\"Slc22a1\"]", "do": null }, { "gene_id": 20518, "description": "solute carrier family 22 (organic cation transporter), member 2", "gene_symbol": "[\"Slc22a2\"]", "do": null }, { "gene_id": 20519, "description": "solute carrier family 22 (organic cation transporter), member 3", "gene_symbol": "[\"Slc22a3\"]", "do": null }, { "gene_id": 20520, "description": "solute carrier family 22 (organic cation transporter), member 5", "gene_symbol": "[\"Slc22a5\"]", "do": "[{\"label\":\"systemic primary carnitine deficiency disease\",\"id\":\"DOID:14365\"}]" }, { "gene_id": 20521, "description": "solute carrier family 22 (organic anion/cation transporter), member 12", "gene_symbol": "[\"Slc22a12\"]", "do": null }, { "gene_id": 20522, "description": "solute carrier family 23 (nucleobase transporters), member 1", "gene_symbol": "[\"Slc23a1\"]", "do": null }, { "gene_id": 20525, "description": "solute carrier family 2 (facilitated glucose transporter), member 1", "gene_symbol": "[\"Slc2a1\"]", "do": "[{\"label\":\"glucose transporter type 1 deficiency syndrome 1\",\"id\":\"DOID:0070561\"}]" }, { "gene_id": 20526, "description": "solute carrier family 2 (facilitated glucose transporter), member 2", "gene_symbol": "[\"Slc2a2\"]", "do": "[{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 20527, "description": "solute carrier family 2 (facilitated glucose transporter), member 3", "gene_symbol": "[\"Slc2a3\"]", "do": null }, { "gene_id": 20528, "description": "solute carrier family 2 (facilitated glucose transporter), member 4", "gene_symbol": "[\"Slc2a4\"]", "do": "[{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 20529, "description": "solute carrier family 31, member 1", "gene_symbol": "[\"Slc31a1\"]", "do": null }, { "gene_id": 20531, "description": "solute carrier family 34 (sodium phosphate), member 2", "gene_symbol": "[\"Slc34a2\"]", "do": null }, { "gene_id": 20532, "description": "solute carrier family 3, member 1", "gene_symbol": "[\"Slc3a1\"]", "do": "[{\"label\":\"cystinuria\",\"id\":\"DOID:9266\"}]" }, { "gene_id": 20533, "description": "solute carrier family 4 (anion exchanger), member 1", "gene_symbol": "[\"Slc4a1\"]", "do": "[{\"label\":\"hereditary spherocytosis type 4\",\"id\":\"DOID:0110919\"},{\"label\":\"renal tubular acidosis\",\"id\":\"DOID:14219\"}]" }, { "gene_id": 20534, "description": "solute carrier family 4 (anion exchanger), member 1, adaptor protein", "gene_symbol": "[\"Slc4a1ap\"]", "do": null }, { "gene_id": 20535, "description": "solute carrier family 4 (anion exchanger), member 2", "gene_symbol": "[\"Slc4a2\"]", "do": null }, { "gene_id": 20536, "description": "solute carrier family 4 (anion exchanger), member 3", "gene_symbol": "[\"Slc4a3\"]", "do": null }, { "gene_id": 20537, "description": "solute carrier family 5 (sodium/glucose cotransporter), member 1", "gene_symbol": "[\"Slc5a1\"]", "do": null }, { "gene_id": 20538, "description": "solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2", "gene_symbol": "[\"Slc6a2\"]", "do": "[{\"label\":\"heart conduction disease\",\"id\":\"DOID:10273\"}]" }, { "gene_id": 20539, "description": "solute carrier family 7 (cationic amino acid transporter, y+ system), member 5", "gene_symbol": "[\"Slc7a5\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 20540, "description": "solute carrier family 7 (cationic amino acid transporter, y+ system), member 7", "gene_symbol": "[\"Slc7a7\"]", "do": "[{\"label\":\"lysinuric protein intolerance\",\"id\":\"DOID:0060439\"}]" }, { "gene_id": 20541, "description": "solute carrier family 8 (sodium/calcium exchanger), member 1", "gene_symbol": "[\"Slc8a1\"]", "do": null }, { "gene_id": 20544, "description": "solute carrier family 9 (sodium/hydrogen exchanger), member 1", "gene_symbol": "[\"Slc9a1\"]", "do": null }, { "gene_id": 20555, "description": "schlafen 1", "gene_symbol": "[\"Slfn1\"]", "do": null }, { "gene_id": 20562, "description": "slit guidance ligand 1", "gene_symbol": "[\"Slit1\"]", "do": null }, { "gene_id": 20563, "description": "slit guidance ligand 2", "gene_symbol": "[\"Slit2\"]", "do": "[{\"label\":\"Kartagener syndrome\",\"id\":\"DOID:0050144\"},{\"label\":\"cystic kidney disease\",\"id\":\"DOID:2975\"},{\"label\":\"primary ciliary dyskinesia\",\"id\":\"DOID:9562\"},{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 20564, "description": "slit guidance ligand 3", "gene_symbol": "[\"Slit3\"]", "do": "[{\"label\":\"congenital diaphragmatic hernia\",\"id\":\"DOID:3827\"}]" }, { "gene_id": 20586, "description": "SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4", "gene_symbol": "[\"Smarca4\"]", "do": "[{\"label\":\"breast cancer\",\"id\":\"DOID:1612\"}]" }, { "gene_id": 20588, "description": "SWI/SNF related BAF chromatin remodeling complex subunit C1", "gene_symbol": "[\"Smarcc1\"]", "do": null }, { "gene_id": 20597, "description": "sphingomyelin phosphodiesterase 1, acid lysosomal", "gene_symbol": "[\"Smpd1\"]", "do": "[{\"label\":\"Niemann-Pick disease\",\"id\":\"DOID:14504\"}]" }, { "gene_id": 20602, "description": "nuclear receptor co-repressor 2", "gene_symbol": "[\"Ncor2\"]", "do": "[{\"label\":\"myelofibrosis\",\"id\":\"DOID:4971\"}]" }, { "gene_id": 20603, "description": "spermine synthase", "gene_symbol": "[\"Sms\"]", "do": null }, { "gene_id": 20605, "description": "somatostatin receptor 1", "gene_symbol": "[\"Sstr1\"]", "do": null }, { "gene_id": 20606, "description": "somatostatin receptor 2", "gene_symbol": "[\"Sstr2\"]", "do": null }, { "gene_id": 20607, "description": "somatostatin receptor 3", "gene_symbol": "[\"Sstr3\"]", "do": null }, { "gene_id": 20608, "description": "somatostatin receptor 4", "gene_symbol": "[\"Sstr4\"]", "do": null }, { "gene_id": 20609, "description": "somatostatin receptor 5", "gene_symbol": "[\"Sstr5\"]", "do": null }, { "gene_id": 20612, "description": "sialic acid binding Ig-like lectin 1, sialoadhesin", "gene_symbol": "[\"Siglec1\"]", "do": null }, { "gene_id": 20613, "description": "snail family zinc finger 1", "gene_symbol": "[\"Snai1\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"},{\"label\":\"skin cancer\",\"id\":\"DOID:4159\"}]" }, { "gene_id": 20614, "description": "synaptosomal-associated protein 25", "gene_symbol": "[\"Snap25\"]", "do": "[{\"label\":\"attention deficit hyperactivity disorder\",\"id\":\"DOID:1094\"},{\"label\":\"obesity\",\"id\":\"DOID:9970\"},{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"},{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 20616, "description": "synaptosomal-associated protein 91", "gene_symbol": "[\"Snap91\"]", "do": null }, { "gene_id": 20617, "description": "synuclein, alpha", "gene_symbol": "[\"Snca\"]", "do": "[{\"label\":\"Parkinson's disease 1\",\"id\":\"DOID:0060367\"},{\"label\":\"Parkinson's disease 4\",\"id\":\"DOID:0060895\"}]" }, { "gene_id": 20618, "description": "synuclein, gamma", "gene_symbol": "[\"Sncg\"]", "do": "[{\"label\":\"amyotrophic lateral sclerosis type 1\",\"id\":\"DOID:0060193\"}]" }, { "gene_id": 20623, "description": "SNF related kinase", "gene_symbol": "[\"Snrk\"]", "do": null }, { "gene_id": 20624, "description": "elongation factor Tu GTP binding domain containing 2", "gene_symbol": "[\"Eftud2\"]", "do": null }, { "gene_id": 20650, "description": "syntrophin, basic 2", "gene_symbol": "[\"Sntb2\"]", "do": null }, { "gene_id": 20655, "description": "superoxide dismutase 1, soluble", "gene_symbol": "[\"Sod1\"]", "do": "[{\"label\":\"amyotrophic lateral sclerosis type 1\",\"id\":\"DOID:0060193\"},{\"label\":\"dry eye syndrome\",\"id\":\"DOID:10140\"},{\"label\":\"low tension glaucoma\",\"id\":\"DOID:13544\"}]" }, { "gene_id": 20656, "description": "superoxide dismutase 2, mitochondrial", "gene_symbol": "[\"Sod2\"]", "do": "[{\"label\":\"Canavan disease\",\"id\":\"DOID:3613\"},{\"label\":\"Leigh disease\",\"id\":\"DOID:3652\"},{\"label\":\"amyotrophic lateral sclerosis type 1\",\"id\":\"DOID:0060193\"},{\"label\":\"congestive heart failure\",\"id\":\"DOID:6000\"},{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 20657, "description": "superoxide dismutase 3, extracellular", "gene_symbol": "[\"Sod3\"]", "do": null }, { "gene_id": 20658, "description": "Son DNA binding protein", "gene_symbol": "[\"Son\"]", "do": null }, { "gene_id": 20660, "description": "sortilin-related receptor, LDLR class A repeats-containing", "gene_symbol": "[\"Sorl1\"]", "do": null }, { "gene_id": 20661, "description": "sortilin 1", "gene_symbol": "[\"Sort1\"]", "do": null }, { "gene_id": 20664, "description": "SRY (sex determining region Y)-box 1", "gene_symbol": "[\"Sox1\"]", "do": null }, { "gene_id": 20666, "description": "SRY (sex determining region Y)-box 11", "gene_symbol": "[\"Sox11\"]", "do": null }, { "gene_id": 20668, "description": "SRY (sex determining region Y)-box 13", "gene_symbol": "[\"Sox13\"]", "do": null }, { "gene_id": 20670, "description": "SRY (sex determining region Y)-box 15", "gene_symbol": "[\"Sox15\"]", "do": null }, { "gene_id": 20674, "description": "SRY (sex determining region Y)-box 2", "gene_symbol": "[\"Sox2\"]", "do": null }, { "gene_id": 20683, "description": "trans-acting transcription factor 1", "gene_symbol": "[\"Sp1\"]", "do": null }, { "gene_id": 20687, "description": "trans-acting transcription factor 3", "gene_symbol": "[\"Sp3\"]", "do": null }, { "gene_id": 20689, "description": "spalt like transcription factor 3", "gene_symbol": "[\"Sall3\"]", "do": null }, { "gene_id": 20690, "description": "sperm adhesion molecule 1", "gene_symbol": "[\"Spam1\"]", "do": null }, { "gene_id": 20692, "description": "secreted acidic cysteine rich glycoprotein", "gene_symbol": "[\"Sparc\"]", "do": null }, { "gene_id": 20700, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 1A", "gene_symbol": "[\"Serpina1a\"]", "do": null }, { "gene_id": 20701, "description": "serine (or cysteine) preptidase inhibitor, clade A, member 1B", "gene_symbol": "[\"Serpina1b\"]", "do": null }, { "gene_id": 20702, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 1C", "gene_symbol": "[\"Serpina1c\"]", "do": null }, { "gene_id": 20703, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 1D", "gene_symbol": "[\"Serpina1d\"]", "do": null }, { "gene_id": 20704, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 1E", "gene_symbol": "[\"Serpina1e\"]", "do": null }, { "gene_id": 20713, "description": "serine (or cysteine) peptidase inhibitor, clade I, member 1", "gene_symbol": "[\"Serpini1\"]", "do": "[{\"label\":\"familial encephalopathy with neuroserpin inclusion bodies\",\"id\":\"DOID:0050831\"}]" }, { "gene_id": 20714, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 3K", "gene_symbol": "[\"Serpina3k\"]", "do": null }, { "gene_id": 20716, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 3N", "gene_symbol": "[\"Serpina3n\"]", "do": null }, { "gene_id": 20717, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 3M", "gene_symbol": "[\"Serpina3m\"]", "do": null }, { "gene_id": 20720, "description": "serine (or cysteine) peptidase inhibitor, clade E, member 2", "gene_symbol": "[\"Serpine2\"]", "do": null }, { "gene_id": 20724, "description": "serine (or cysteine) peptidase inhibitor, clade B, member 5", "gene_symbol": "[\"Serpinb5\"]", "do": null }, { "gene_id": 20728, "description": "Spi-C transcription factor (Spi-1/PU.1 related)", "gene_symbol": "[\"Spic\"]", "do": null }, { "gene_id": 20729, "description": "spindlin 1", "gene_symbol": "[\"Spin1\"]", "do": null }, { "gene_id": 20732, "description": "serine protease inhibitor, Kunitz type 1", "gene_symbol": "[\"Spint1\"]", "do": null }, { "gene_id": 20733, "description": "serine protease inhibitor, Kunitz type 2", "gene_symbol": "[\"Spint2\"]", "do": null }, { "gene_id": 20737, "description": "sialophorin", "gene_symbol": "[\"Spn\"]", "do": null }, { "gene_id": 20739, "description": "spectrin alpha, erythrocytic 1", "gene_symbol": "[\"Spta1\"]", "do": "[{\"label\":\"hereditary spherocytosis type 1\",\"id\":\"DOID:0110916\"},{\"label\":\"hereditary spherocytosis type 3\",\"id\":\"DOID:0110918\"},{\"label\":\"sickle cell anemia\",\"id\":\"DOID:10923\"}]" }, { "gene_id": 20740, "description": "spectrin alpha, non-erythrocytic 1", "gene_symbol": "[\"Sptan1\"]", "do": null }, { "gene_id": 20742, "description": "spectrin beta, non-erythrocytic 1", "gene_symbol": "[\"Sptbn1\"]", "do": "[{\"label\":\"Beckwith-Wiedemann syndrome\",\"id\":\"DOID:5572\"}]" }, { "gene_id": 20750, "description": "secreted phosphoprotein 1", "gene_symbol": "[\"Spp1\"]", "do": null }, { "gene_id": 20753, "description": "small proline-rich protein 1A", "gene_symbol": "[\"Sprr1a\"]", "do": null }, { "gene_id": 20770, "description": "mucin-like 2", "gene_symbol": "[\"Mucl2\"]", "do": null }, { "gene_id": 20773, "description": "serine palmitoyltransferase, long chain base subunit 2", "gene_symbol": "[\"Sptlc2\"]", "do": "[{\"label\":\"psoriasis\",\"id\":\"DOID:8893\"}]" }, { "gene_id": 20778, "description": "scavenger receptor class B, member 1", "gene_symbol": "[\"Scarb1\"]", "do": null }, { "gene_id": 20779, "description": "src proto-oncogene, non-receptor tyrosine kinase", "gene_symbol": "[\"Src\"]", "do": "[{\"label\":\"Williams-Beuren syndrome\",\"id\":\"DOID:1928\"}]" }, { "gene_id": 20787, "description": "sterol regulatory element binding transcription factor 1", "gene_symbol": "[\"Srebf1\"]", "do": null }, { "gene_id": 20788, "description": "sterol regulatory element binding factor 2", "gene_symbol": "[\"Srebf2\"]", "do": null }, { "gene_id": 20807, "description": "serum response factor", "gene_symbol": "[\"Srf\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 20815, "description": "serine/arginine-rich protein specific kinase 1", "gene_symbol": "[\"Srpk1\"]", "do": null }, { "gene_id": 20817, "description": "serine/arginine-rich protein specific kinase 2", "gene_symbol": "[\"Srpk2\"]", "do": null }, { "gene_id": 20833, "description": "structure specific recognition protein 1", "gene_symbol": "[\"Ssrp1\"]", "do": null }, { "gene_id": 20834, "description": "zinc and ring finger 4", "gene_symbol": "[\"Znrf4\"]", "do": null }, { "gene_id": 20840, "description": "src homology three (SH3) and cysteine rich domain", "gene_symbol": "[\"Stac\"]", "do": null }, { "gene_id": 20844, "description": "signal transducing adaptor molecule (SH3 domain and ITAM motif) 1", "gene_symbol": "[\"Stam\"]", "do": null }, { "gene_id": 20848, "description": "signal transducer and activator of transcription 3", "gene_symbol": "[\"Stat3\"]", "do": "[{\"label\":\"autosomal dominant hyper-IgE syndrome 1 with recurrent infections\",\"id\":\"DOID:3261\"},{\"label\":\"colorectal cancer\",\"id\":\"DOID:9256\"},{\"label\":\"inflammatory bowel disease\",\"id\":\"DOID:0050589\"},{\"label\":\"peripartum cardiomyopathy\",\"id\":\"DOID:9997\"},{\"label\":\"psoriasis\",\"id\":\"DOID:8893\"}]" }, { "gene_id": 20850, "description": "signal transducer and activator of transcription 5A", "gene_symbol": "[\"Stat5a\"]", "do": null }, { "gene_id": 20851, "description": "signal transducer and activator of transcription 5B", "gene_symbol": "[\"Stat5b\"]", "do": null }, { "gene_id": 20852, "description": "signal transducer and activator of transcription 6", "gene_symbol": "[\"Stat6\"]", "do": null }, { "gene_id": 20853, "description": "staufen double-stranded RNA binding protein 1", "gene_symbol": "[\"Stau1\"]", "do": null }, { "gene_id": 20855, "description": "stanniocalcin 1", "gene_symbol": "[\"Stc1\"]", "do": null }, { "gene_id": 20856, "description": "stanniocalcin 2", "gene_symbol": "[\"Stc2\"]", "do": null }, { "gene_id": 20866, "description": "stromal interaction molecule 1", "gene_symbol": "[\"Stim1\"]", "do": "[{\"label\":\"Stormorken syndrome\",\"id\":\"DOID:0060354\"},{\"label\":\"tubular aggregate myopathy 1\",\"id\":\"DOID:0080089\"}]" }, { "gene_id": 20868, "description": "serine/threonine kinase 10", "gene_symbol": "[\"Stk10\"]", "do": null }, { "gene_id": 20873, "description": "polo like kinase 4", "gene_symbol": "[\"Plk4\"]", "do": null }, { "gene_id": 20874, "description": "STE20-like kinase", "gene_symbol": "[\"Slk\"]", "do": null }, { "gene_id": 20877, "description": "aurora kinase B", "gene_symbol": "[\"Aurkb\"]", "do": null }, { "gene_id": 20890, "description": "wingless-type MMTV integration site family, member 8A", "gene_symbol": "[\"Wnt8a\"]", "do": null }, { "gene_id": 20897, "description": "stimulated by retinoic acid gene 6", "gene_symbol": "[\"Stra6\"]", "do": null }, { "gene_id": 20905, "description": "steroid sulfatase", "gene_symbol": "[\"Sts\"]", "do": null }, { "gene_id": 20907, "description": "syntaxin 1A (brain)", "gene_symbol": "[\"Stx1a\"]", "do": "[{\"label\":\"disease of mental health\",\"id\":\"DOID:150\"}]" }, { "gene_id": 20910, "description": "syntaxin binding protein 1", "gene_symbol": "[\"Stxbp1\"]", "do": null }, { "gene_id": 20916, "description": "succinate-Coenzyme A ligase, ADP-forming, beta subunit", "gene_symbol": "[\"Sucla2\"]", "do": "[{\"label\":\"mitochondrial DNA depletion syndrome 5\",\"id\":\"DOID:0080124\"}]" }, { "gene_id": 20924, "description": "suppressor of Ty 5, DSIF elongation factor subunit", "gene_symbol": "[\"Supt5\"]", "do": null }, { "gene_id": 20926, "description": "SPT6, histone chaperone and transcription elongation factor", "gene_symbol": "[\"Supt6\"]", "do": null }, { "gene_id": 20927, "description": "ATP-binding cassette, sub-family C member 8", "gene_symbol": "[\"Abcc8\"]", "do": "[{\"label\":\"hyperinsulinemic hypoglycemia\",\"id\":\"DOID:13317\"},{\"label\":\"transient neonatal diabetes mellitus\",\"id\":\"DOID:0060334\"}]" }, { "gene_id": 20928, "description": "ATP-binding cassette, sub-family C member 9", "gene_symbol": "[\"Abcc9\"]", "do": "[{\"label\":\"hypertrichotic osteochondrodysplasia Cantu type\",\"id\":\"DOID:0060569\"}]" }, { "gene_id": 20935, "description": "surfeit gene 6", "gene_symbol": "[\"Surf6\"]", "do": null }, { "gene_id": 20939, "description": "seminal vesicle antigen", "gene_symbol": "[\"Sva\"]", "do": null }, { "gene_id": 20964, "description": "synapsin I", "gene_symbol": "[\"Syn1\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 20965, "description": "synapsin II", "gene_symbol": "[\"Syn2\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"epilepsy\",\"id\":\"DOID:1826\"}]" }, { "gene_id": 20969, "description": "syndecan 1", "gene_symbol": "[\"Sdc1\"]", "do": null }, { "gene_id": 20970, "description": "syndecan 3", "gene_symbol": "[\"Sdc3\"]", "do": null }, { "gene_id": 20971, "description": "syndecan 4", "gene_symbol": "[\"Sdc4\"]", "do": null }, { "gene_id": 20972, "description": "synaptogyrin 1", "gene_symbol": "[\"Syngr1\"]", "do": null }, { "gene_id": 20975, "description": "synaptojanin 2", "gene_symbol": "[\"Synj2\"]", "do": null }, { "gene_id": 20977, "description": "synaptophysin", "gene_symbol": "[\"Syp\"]", "do": null }, { "gene_id": 20979, "description": "synaptotagmin I", "gene_symbol": "[\"Syt1\"]", "do": null }, { "gene_id": 20980, "description": "synaptotagmin II", "gene_symbol": "[\"Syt2\"]", "do": null }, { "gene_id": 21336, "description": "tachykinin receptor 1", "gene_symbol": "[\"Tacr1\"]", "do": "[{\"label\":\"attention deficit hyperactivity disorder\",\"id\":\"DOID:1094\"}]" }, { "gene_id": 21337, "description": "tachykinin receptor 2", "gene_symbol": "[\"Tacr2\"]", "do": null }, { "gene_id": 21338, "description": "tachykinin receptor 3", "gene_symbol": "[\"Tacr3\"]", "do": "[{\"label\":\"hypogonadotropic hypogonadism 11 with or without anosmia\",\"id\":\"DOID:0090071\"}]" }, { "gene_id": 21343, "description": "TATA-box binding protein associated factor 6", "gene_symbol": "[\"Taf6\"]", "do": null }, { "gene_id": 21346, "description": "transgelin 2", "gene_symbol": "[\"Tagln2\"]", "do": null }, { "gene_id": 21351, "description": "transaldolase 1", "gene_symbol": "[\"Taldo1\"]", "do": null }, { "gene_id": 21353, "description": "TRAF family member-associated Nf-kappa B activator", "gene_symbol": "[\"Tank\"]", "do": null }, { "gene_id": 21356, "description": "TAP binding protein", "gene_symbol": "[\"Tapbp\"]", "do": null }, { "gene_id": 21366, "description": "solute carrier family 6 (neurotransmitter transporter, taurine), member 6", "gene_symbol": "[\"Slc6a6\"]", "do": "[{\"label\":\"retinitis pigmentosa\",\"id\":\"DOID:10584\"}]" }, { "gene_id": 21367, "description": "contactin 2", "gene_symbol": "[\"Cntn2\"]", "do": "[{\"label\":\"T-cell adult acute lymphocytic leukemia\",\"id\":\"DOID:5602\"}]" }, { "gene_id": 21372, "description": "transducin beta like 1 X-linked", "gene_symbol": "[\"Tbl1x\"]", "do": null }, { "gene_id": 21375, "description": "T-box brain transcription factor 1", "gene_symbol": "[\"Tbr1\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 21386, "description": "T-box 3", "gene_symbol": "[\"Tbx3\"]", "do": "[{\"label\":\"ulnar-mammary syndrome\",\"id\":\"DOID:0060614\"}]" }, { "gene_id": 21390, "description": "thromboxane A2 receptor", "gene_symbol": "[\"Tbxa2r\"]", "do": null }, { "gene_id": 21406, "description": "transcription factor 12", "gene_symbol": "[\"Tcf12\"]", "do": null }, { "gene_id": 21411, "description": "transcription factor 20", "gene_symbol": "[\"Tcf20\"]", "do": "[{\"label\":\"Phelan-McDermid syndrome\",\"id\":\"DOID:0080354\"},{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 21413, "description": "transcription factor 4", "gene_symbol": "[\"Tcf4\"]", "do": "[{\"label\":\"Pitt-Hopkins syndrome\",\"id\":\"DOID:0060488\"},{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 21416, "description": "transcription factor 7 like 2, T cell specific, HMG box", "gene_symbol": "[\"Tcf7l2\"]", "do": null }, { "gene_id": 21419, "description": "transcription factor AP-2 beta", "gene_symbol": "[\"Tfap2b\"]", "do": "[{\"label\":\"Char syndrome\",\"id\":\"DOID:0060563\"},{\"label\":\"angle-closure glaucoma\",\"id\":\"DOID:13550\"},{\"label\":\"patent ductus arteriosus\",\"id\":\"DOID:13832\"}]" }, { "gene_id": 21453, "description": "treacle ribosome biogenesis factor 1", "gene_symbol": "[\"Tcof1\"]", "do": "[{\"label\":\"Treacher Collins syndrome\",\"id\":\"DOID:2908\"}]" }, { "gene_id": 21665, "description": "thymine DNA glycosylase", "gene_symbol": "[\"Tdg\"]", "do": null }, { "gene_id": 21667, "description": "cripto, EGF-CFC family member", "gene_symbol": "[\"Cripto\"]", "do": null }, { "gene_id": 21683, "description": "tectorin alpha", "gene_symbol": "[\"Tecta\"]", "do": "[{\"label\":\"autosomal dominant nonsyndromic deafness 12\",\"id\":\"DOID:0110544\"}]" }, { "gene_id": 21684, "description": "tectorin beta", "gene_symbol": "[\"Tectb\"]", "do": null }, { "gene_id": 21687, "description": "TEK receptor tyrosine kinase", "gene_symbol": "[\"Tek\"]", "do": null }, { "gene_id": 21745, "description": "telomerase associated protein 1", "gene_symbol": "[\"Tep1\"]", "do": null }, { "gene_id": 21755, "description": "serine protease 39", "gene_symbol": "[\"Prss39\"]", "do": null }, { "gene_id": 21756, "description": "serine protease 40", "gene_symbol": "[\"Prss40\"]", "do": null }, { "gene_id": 21762, "description": "proteasome (prosome, macropain) 26S subunit, non-ATPase, 2", "gene_symbol": "[\"Psmd2\"]", "do": null }, { "gene_id": 21763, "description": "testis expressed gene 2", "gene_symbol": "[\"Tex2\"]", "do": null }, { "gene_id": 21770, "description": "protein phosphatase 2, regulatory subunit B', delta", "gene_symbol": "[\"Ppp2r5d\"]", "do": null }, { "gene_id": 21787, "description": "Trk-fused gene", "gene_symbol": "[\"Tfg\"]", "do": null }, { "gene_id": 21788, "description": "tissue factor pathway inhibitor", "gene_symbol": "[\"Tfpi\"]", "do": null }, { "gene_id": 21789, "description": "tissue factor pathway inhibitor 2", "gene_symbol": "[\"Tfpi2\"]", "do": null }, { "gene_id": 21802, "description": "transforming growth factor alpha", "gene_symbol": "[\"Tgfa\"]", "do": null }, { "gene_id": 21803, "description": "transforming growth factor, beta 1", "gene_symbol": "[\"Tgfb1\"]", "do": "[{\"label\":\"Sjogren's syndrome\",\"id\":\"DOID:12894\"}]" }, { "gene_id": 21807, "description": "TSC22 domain family, member 1", "gene_symbol": "[\"Tsc22d1\"]", "do": null }, { "gene_id": 21808, "description": "transforming growth factor, beta 2", "gene_symbol": "[\"Tgfb2\"]", "do": "[{\"label\":\"Loeys-Dietz syndrome\",\"id\":\"DOID:0050466\"}]" }, { "gene_id": 21809, "description": "transforming growth factor, beta 3", "gene_symbol": "[\"Tgfb3\"]", "do": null }, { "gene_id": 21812, "description": "transforming growth factor, beta receptor I", "gene_symbol": "[\"Tgfbr1\"]", "do": "[{\"label\":\"Loeys-Dietz syndrome\",\"id\":\"DOID:0050466\"},{\"label\":\"osteoarthritis\",\"id\":\"DOID:8398\"},{\"label\":\"systemic scleroderma\",\"id\":\"DOID:418\"}]" }, { "gene_id": 21813, "description": "transforming growth factor, beta receptor II", "gene_symbol": "[\"Tgfbr2\"]", "do": "[{\"label\":\"DiGeorge syndrome\",\"id\":\"DOID:11198\"},{\"label\":\"Loeys-Dietz syndrome\",\"id\":\"DOID:0050466\"},{\"label\":\"cleft soft palate\",\"id\":\"DOID:0110214\"},{\"label\":\"prostate cancer\",\"id\":\"DOID:10283\"}]" }, { "gene_id": 21814, "description": "transforming growth factor, beta receptor III", "gene_symbol": "[\"Tgfbr3\"]", "do": null }, { "gene_id": 21817, "description": "transglutaminase 2, C polypeptide", "gene_symbol": "[\"Tgm2\"]", "do": "[{\"label\":\"maturity-onset diabetes of the young\",\"id\":\"DOID:0050524\"}]" }, { "gene_id": 21819, "description": "thyroglobulin", "gene_symbol": "[\"Tg\"]", "do": "[{\"label\":\"congenital hypothyroidism\",\"id\":\"DOID:0050328\"}]" }, { "gene_id": 21823, "description": "tyrosine hydroxylase", "gene_symbol": "[\"Th\"]", "do": null }, { "gene_id": 21824, "description": "thrombomodulin", "gene_symbol": "[\"Thbd\"]", "do": "[{\"label\":\"thrombophilia\",\"id\":\"DOID:2452\"}]" }, { "gene_id": 21825, "description": "thrombospondin 1", "gene_symbol": "[\"Thbs1\"]", "do": "[{\"label\":\"Sjogren's syndrome\",\"id\":\"DOID:12894\"}]" }, { "gene_id": 21826, "description": "thrombospondin 2", "gene_symbol": "[\"Thbs2\"]", "do": null }, { "gene_id": 21827, "description": "thrombospondin 3", "gene_symbol": "[\"Thbs3\"]", "do": null }, { "gene_id": 21828, "description": "thrombospondin 4", "gene_symbol": "[\"Thbs4\"]", "do": null }, { "gene_id": 21832, "description": "thrombopoietin", "gene_symbol": "[\"Thpo\"]", "do": null }, { "gene_id": 21838, "description": "thymus cell antigen 1, theta", "gene_symbol": "[\"Thy1\"]", "do": null }, { "gene_id": 21846, "description": "tyrosine kinase with immunoglobulin-like and EGF-like domains 1", "gene_symbol": "[\"Tie1\"]", "do": null }, { "gene_id": 21848, "description": "tripartite motif-containing 24", "gene_symbol": "[\"Trim24\"]", "do": null }, { "gene_id": 21849, "description": "tripartite motif-containing 28", "gene_symbol": "[\"Trim28\"]", "do": null }, { "gene_id": 21853, "description": "timeless circadian clock 1", "gene_symbol": "[\"Timeless\"]", "do": null }, { "gene_id": 21857, "description": "tissue inhibitor of metalloproteinase 1", "gene_symbol": "[\"Timp1\"]", "do": null }, { "gene_id": 21859, "description": "tissue inhibitor of metalloproteinase 3", "gene_symbol": "[\"Timp3\"]", "do": "[{\"label\":\"Sorsby's fundus dystrophy\",\"id\":\"DOID:0090114\"},{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 21871, "description": "ATPase, H+ transporting, lysosomal V0 subunit A2", "gene_symbol": "[\"Atp6v0a2\"]", "do": null }, { "gene_id": 21872, "description": "tight junction protein 1", "gene_symbol": "[\"Tjp1\"]", "do": null }, { "gene_id": 21873, "description": "tight junction protein 2", "gene_symbol": "[\"Tjp2\"]", "do": null }, { "gene_id": 21881, "description": "transketolase", "gene_symbol": "[\"Tkt\"]", "do": null }, { "gene_id": 21885, "description": "transducin-like enhancer of split 1", "gene_symbol": "[\"Tle1\"]", "do": null }, { "gene_id": 21886, "description": "transducin-like enhancer of split 2", "gene_symbol": "[\"Tle2\"]", "do": null }, { "gene_id": 21887, "description": "transducin-like enhancer of split 3", "gene_symbol": "[\"Tle3\"]", "do": null }, { "gene_id": 21888, "description": "transducin-like enhancer of split 4", "gene_symbol": "[\"Tle4\"]", "do": null }, { "gene_id": 21894, "description": "talin 1", "gene_symbol": "[\"Tln1\"]", "do": null }, { "gene_id": 21897, "description": "toll-like receptor 1", "gene_symbol": "[\"Tlr1\"]", "do": null }, { "gene_id": 21898, "description": "toll-like receptor 4", "gene_symbol": "[\"Tlr4\"]", "do": "[{\"label\":\"pulmonary emphysema\",\"id\":\"DOID:9675\"}]" }, { "gene_id": 21899, "description": "toll-like receptor 6", "gene_symbol": "[\"Tlr6\"]", "do": null }, { "gene_id": 21907, "description": "nuclear receptor subfamily 2, group E, member 1", "gene_symbol": "[\"Nr2e1\"]", "do": null }, { "gene_id": 21912, "description": "tetraspanin 7", "gene_symbol": "[\"Tspan7\"]", "do": null }, { "gene_id": 21917, "description": "thymopoietin", "gene_symbol": "[\"Tmpo\"]", "do": null }, { "gene_id": 21923, "description": "tenascin C", "gene_symbol": "[\"Tnc\"]", "do": null }, { "gene_id": 21926, "description": "tumor necrosis factor", "gene_symbol": "[\"Tnf\"]", "do": "[{\"label\":\"aortic valve stenosis\",\"id\":\"DOID:1712\"},{\"label\":\"congestive heart failure\",\"id\":\"DOID:6000\"},{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"},{\"label\":\"heart valve disease\",\"id\":\"DOID:4079\"},{\"label\":\"idiopathic pulmonary fibrosis\",\"id\":\"DOID:0050156\"},{\"label\":\"inflammatory bowel disease\",\"id\":\"DOID:0050589\"},{\"label\":\"multiple sclerosis\",\"id\":\"DOID:2377\"},{\"label\":\"rheumatoid arthritis\",\"id\":\"DOID:7148\"},{\"label\":\"spondyloarthropathy\",\"id\":\"DOID:1123\"}]" }, { "gene_id": 21929, "description": "tumor necrosis factor, alpha-induced protein 3", "gene_symbol": "[\"Tnfaip3\"]", "do": null }, { "gene_id": 21930, "description": "tumor necrosis factor alpha induced protein 6", "gene_symbol": "[\"Tnfaip6\"]", "do": null }, { "gene_id": 21933, "description": "tumor necrosis factor receptor superfamily, member 10b", "gene_symbol": "[\"Tnfrsf10b\"]", "do": null }, { "gene_id": 21934, "description": "tumor necrosis factor receptor superfamily, member 11a, NFKB activator", "gene_symbol": "[\"Tnfrsf11a\"]", "do": "[{\"label\":\"Paget's disease of bone\",\"id\":\"DOID:5408\"}]" }, { "gene_id": 21936, "description": "tumor necrosis factor receptor superfamily, member 18", "gene_symbol": "[\"Tnfrsf18\"]", "do": null }, { "gene_id": 21937, "description": "tumor necrosis factor receptor superfamily, member 1a", "gene_symbol": "[\"Tnfrsf1a\"]", "do": "[{\"label\":\"TNF receptor–associated periodic syndrome\",\"id\":\"DOID:0090018\"}]" }, { "gene_id": 21938, "description": "tumor necrosis factor receptor superfamily, member 1b", "gene_symbol": "[\"Tnfrsf1b\"]", "do": null }, { "gene_id": 21939, "description": "CD40 antigen", "gene_symbol": "[\"Cd40\"]", "do": null }, { "gene_id": 21940, "description": "CD27 antigen", "gene_symbol": "[\"Cd27\"]", "do": null }, { "gene_id": 21941, "description": "tumor necrosis factor receptor superfamily, member 8", "gene_symbol": "[\"Tnfrsf8\"]", "do": null }, { "gene_id": 21942, "description": "tumor necrosis factor receptor superfamily, member 9", "gene_symbol": "[\"Tnfrsf9\"]", "do": null }, { "gene_id": 21943, "description": "tumor necrosis factor (ligand) superfamily, member 11", "gene_symbol": "[\"Tnfsf11\"]", "do": "[{\"label\":\"autosomal recessive osteopetrosis 2\",\"id\":\"DOID:0110943\"},{\"label\":\"osteoporosis\",\"id\":\"DOID:11476\"}]" }, { "gene_id": 21944, "description": "tumor necrosis factor (ligand) superfamily, member 12", "gene_symbol": "[\"Tnfsf12\"]", "do": null }, { "gene_id": 21947, "description": "CD40 ligand", "gene_symbol": "[\"Cd40lg\"]", "do": "[{\"label\":\"inflammatory bowel disease\",\"id\":\"DOID:0050589\"},{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 21948, "description": "CD70 antigen", "gene_symbol": "[\"Cd70\"]", "do": null }, { "gene_id": 21949, "description": "tumor necrosis factor (ligand) superfamily, member 8", "gene_symbol": "[\"Tnfsf8\"]", "do": null }, { "gene_id": 21950, "description": "tumor necrosis factor (ligand) superfamily, member 9", "gene_symbol": "[\"Tnfsf9\"]", "do": null }, { "gene_id": 21951, "description": "tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase", "gene_symbol": "[\"Tnks\"]", "do": null }, { "gene_id": 21954, "description": "troponin I, cardiac 3", "gene_symbol": "[\"Tnni3\"]", "do": "[{\"label\":\"hypertrophic cardiomyopathy 7\",\"id\":\"DOID:0110313\"},{\"label\":\"restrictive cardiomyopathy\",\"id\":\"DOID:397\"}]" }, { "gene_id": 21960, "description": "tenascin R", "gene_symbol": "[\"Tnr\"]", "do": null }, { "gene_id": 21961, "description": "tensin 1", "gene_symbol": "[\"Tns1\"]", "do": null }, { "gene_id": 21968, "description": "target of myb1 trafficking protein", "gene_symbol": "[\"Tom1\"]", "do": null }, { "gene_id": 21969, "description": "topoisomerase (DNA) I", "gene_symbol": "[\"Top1\"]", "do": null }, { "gene_id": 21973, "description": "topoisomerase (DNA) II alpha", "gene_symbol": "[\"Top2a\"]", "do": null }, { "gene_id": 21974, "description": "topoisomerase (DNA) II beta", "gene_symbol": "[\"Top2b\"]", "do": null }, { "gene_id": 21981, "description": "protein phosphatase 1, regulatory subunit 13B", "gene_symbol": "[\"Ppp1r13b\"]", "do": null }, { "gene_id": 21983, "description": "trophoblast glycoprotein", "gene_symbol": "[\"Tpbg\"]", "do": null }, { "gene_id": 21991, "description": "triosephosphate isomerase 1", "gene_symbol": "[\"Tpi1\"]", "do": "[{\"label\":\"triosephosphate isomerase deficiency\",\"id\":\"DOID:0050884\"}]" }, { "gene_id": 22018, "description": "thyroid peroxidase", "gene_symbol": "[\"Tpo\"]", "do": "[{\"label\":\"congenital hypothyroidism\",\"id\":\"DOID:0050328\"}]" }, { "gene_id": 22019, "description": "tripeptidyl peptidase II", "gene_symbol": "[\"Tpp2\"]", "do": null }, { "gene_id": 22021, "description": "protein-tyrosine sulfotransferase 1", "gene_symbol": "[\"Tpst1\"]", "do": null }, { "gene_id": 22022, "description": "protein-tyrosine sulfotransferase 2", "gene_symbol": "[\"Tpst2\"]", "do": null }, { "gene_id": 22027, "description": "heat shock protein 90, beta (Grp94), member 1", "gene_symbol": "[\"Hsp90b1\"]", "do": "[{\"label\":\"male infertility due to globozoospermia\",\"id\":\"DOID:0112312\"}]" }, { "gene_id": 22033, "description": "TNF receptor-associated factor 5", "gene_symbol": "[\"Traf5\"]", "do": null }, { "gene_id": 22035, "description": "tumor necrosis factor (ligand) superfamily, member 10", "gene_symbol": "[\"Tnfsf10\"]", "do": null }, { "gene_id": 22038, "description": "phospholipid scramblase 1", "gene_symbol": "[\"Plscr1\"]", "do": null }, { "gene_id": 22041, "description": "transferrin", "gene_symbol": "[\"Trf\"]", "do": "[{\"label\":\"atransferrinemia\",\"id\":\"DOID:0050649\"}]" }, { "gene_id": 22042, "description": "transferrin receptor", "gene_symbol": "[\"Tfrc\"]", "do": "[{\"label\":\"Weissenbacher-Zweymuller syndrome\",\"id\":\"DOID:4258\"}]" }, { "gene_id": 22045, "description": "thyrotropin releasing hormone receptor", "gene_symbol": "[\"Trhr\"]", "do": "[{\"label\":\"congenital hypothyroidism\",\"id\":\"DOID:0050328\"}]" }, { "gene_id": 22051, "description": "thyroid hormone receptor interactor 6", "gene_symbol": "[\"Trip6\"]", "do": null }, { "gene_id": 22057, "description": "transducer of ErbB-2.1", "gene_symbol": "[\"Tob1\"]", "do": null }, { "gene_id": 22059, "description": "transformation related protein 53", "gene_symbol": "[\"Trp53\"]", "do": "[{\"label\":\"CHARGE syndrome\",\"id\":\"DOID:0050834\"},{\"label\":\"Li-Fraumeni syndrome\",\"id\":\"DOID:3012\"},{\"label\":\"breast cancer\",\"id\":\"DOID:1612\"},{\"label\":\"diffuse large B-cell lymphoma\",\"id\":\"DOID:0050745\"},{\"label\":\"dyskeratosis congenita\",\"id\":\"DOID:2729\"},{\"label\":\"endometrial cancer\",\"id\":\"DOID:1380\"},{\"label\":\"glioblastoma\",\"id\":\"DOID:3068\"},{\"label\":\"osteosarcoma\",\"id\":\"DOID:3347\"}]" }, { "gene_id": 22065, "description": "transient receptor potential cation channel, subfamily C, member 3", "gene_symbol": "[\"Trpc3\"]", "do": null }, { "gene_id": 22067, "description": "transient receptor potential cation channel, subfamily C, member 5", "gene_symbol": "[\"Trpc5\"]", "do": null }, { "gene_id": 22068, "description": "transient receptor potential cation channel, subfamily C, member 6", "gene_symbol": "[\"Trpc6\"]", "do": "[{\"label\":\"focal segmental glomerulosclerosis 2\",\"id\":\"DOID:0111129\"}]" }, { "gene_id": 22095, "description": "thyroid stimulating hormone receptor", "gene_symbol": "[\"Tshr\"]", "do": "[{\"label\":\"congenital hypothyroidism\",\"id\":\"DOID:0050328\"}]" }, { "gene_id": 22117, "description": "thiosulfate sulfurtransferase, mitochondrial", "gene_symbol": "[\"Tst\"]", "do": null }, { "gene_id": 22121, "description": "ribosomal protein L13A", "gene_symbol": "[\"Rpl13a\"]", "do": null }, { "gene_id": 22123, "description": "proteasome (prosome, macropain) 26S subunit, non-ATPase, 3", "gene_symbol": "[\"Psmd3\"]", "do": null }, { "gene_id": 22134, "description": "trans-golgi network protein", "gene_symbol": "[\"Tgoln1\"]", "do": null }, { "gene_id": 22135, "description": "trans-golgi network protein 2", "gene_symbol": "[\"Tgoln2\"]", "do": null }, { "gene_id": 22138, "description": "titin", "gene_symbol": "[\"Ttn\"]", "do": "[{\"label\":\"autosomal recessive limb-girdle muscular dystrophy type 2J\",\"id\":\"DOID:0110283\"},{\"label\":\"dilated cardiomyopathy 1G\",\"id\":\"DOID:0110430\"},{\"label\":\"tibial muscular dystrophy\",\"id\":\"DOID:0111078\"}]" }, { "gene_id": 22139, "description": "transthyretin", "gene_symbol": "[\"Ttr\"]", "do": "[{\"label\":\"hereditary systemic amyloidosis 1\",\"id\":\"DOID:0050638\"}]" }, { "gene_id": 22142, "description": "tubulin, alpha 1A", "gene_symbol": "[\"Tuba1a\"]", "do": "[{\"label\":\"congenital nervous system abnormality\",\"id\":\"DOID:2490\"},{\"label\":\"lissencephaly\",\"id\":\"DOID:0050453\"}]" }, { "gene_id": 22143, "description": "tubulin, alpha 1B", "gene_symbol": "[\"Tuba1b\"]", "do": null }, { "gene_id": 22144, "description": "tubulin, alpha 3A", "gene_symbol": "[\"Tuba3a\"]", "do": null }, { "gene_id": 22145, "description": "tubulin, alpha 4A", "gene_symbol": "[\"Tuba4a\"]", "do": null }, { "gene_id": 22146, "description": "tubulin, alpha 1C", "gene_symbol": "[\"Tuba1c\"]", "do": null }, { "gene_id": 22147, "description": "tubulin, alpha 3B", "gene_symbol": "[\"Tuba3b\"]", "do": null }, { "gene_id": 22151, "description": "tubulin, beta 2A class IIA", "gene_symbol": "[\"Tubb2a\"]", "do": null }, { "gene_id": 22152, "description": "tubulin, beta 3 class III", "gene_symbol": "[\"Tubb3\"]", "do": "[{\"label\":\"congenital fibrosis of the extraocular muscles\",\"id\":\"DOID:0080143\"}]" }, { "gene_id": 22153, "description": "tubulin, beta 4A class IVA", "gene_symbol": "[\"Tubb4a\"]", "do": "[{\"label\":\"hypomyelinating leukodystrophy 6\",\"id\":\"DOID:0060798\"}]" }, { "gene_id": 22154, "description": "tubulin, beta 5 class I", "gene_symbol": "[\"Tubb5\"]", "do": "[{\"label\":\"microcephaly\",\"id\":\"DOID:10907\"}]" }, { "gene_id": 22157, "description": "TUB like protein 1", "gene_symbol": "[\"Tulp1\"]", "do": "[{\"label\":\"retinitis pigmentosa 14\",\"id\":\"DOID:0110381\"}]" }, { "gene_id": 22163, "description": "tumor necrosis factor receptor superfamily, member 4", "gene_symbol": "[\"Tnfrsf4\"]", "do": null }, { "gene_id": 22164, "description": "tumor necrosis factor (ligand) superfamily, member 4", "gene_symbol": "[\"Tnfsf4\"]", "do": "[{\"label\":\"primary pulmonary hypertension\",\"id\":\"DOID:14557\"},{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 22173, "description": "tyrosinase", "gene_symbol": "[\"Tyr\"]", "do": "[{\"label\":\"buphthalmos\",\"id\":\"DOID:11211\"},{\"label\":\"oculocutaneous albinism\",\"id\":\"DOID:0050632\"}]" }, { "gene_id": 22174, "description": "TYRO3 protein tyrosine kinase 3", "gene_symbol": "[\"Tyro3\"]", "do": null }, { "gene_id": 22178, "description": "tyrosinase-related protein 1", "gene_symbol": "[\"Tyrp1\"]", "do": null }, { "gene_id": 22185, "description": "U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2", "gene_symbol": "[\"U2af2\"]", "do": null }, { "gene_id": 22187, "description": "ubiquitin B", "gene_symbol": "[\"Ubb\"]", "do": null }, { "gene_id": 22200, "description": "ubiquitin-like modifier activating enzyme 3", "gene_symbol": "[\"Uba3\"]", "do": null }, { "gene_id": 22201, "description": "ubiquitin-like modifier activating enzyme 1", "gene_symbol": "[\"Uba1\"]", "do": null }, { "gene_id": 22222, "description": "ubiquitin protein ligase E3 component n-recognin 1", "gene_symbol": "[\"Ubr1\"]", "do": null }, { "gene_id": 22224, "description": "ubiquitin specific peptidase 10", "gene_symbol": "[\"Usp10\"]", "do": null }, { "gene_id": 22228, "description": "uncoupling protein 2 (mitochondrial, proton carrier)", "gene_symbol": "[\"Ucp2\"]", "do": "[{\"label\":\"polycystic liver disease\",\"id\":\"DOID:0050770\"}]" }, { "gene_id": 22234, "description": "UDP-glucose ceramide glucosyltransferase", "gene_symbol": "[\"Ugcg\"]", "do": null }, { "gene_id": 22235, "description": "UDP-glucose dehydrogenase", "gene_symbol": "[\"Ugdh\"]", "do": null }, { "gene_id": 22236, "description": "UDP glucuronosyltransferase 1 family, polypeptide A2", "gene_symbol": "[\"Ugt1a2\"]", "do": null }, { "gene_id": 22238, "description": "UDP glucuronosyltransferase 2 family, polypeptide B5", "gene_symbol": "[\"Ugt2b5\"]", "do": null }, { "gene_id": 22239, "description": "UDP galactosyltransferase 8A", "gene_symbol": "[\"Ugt8a\"]", "do": null }, { "gene_id": 22240, "description": "dihydropyrimidinase-like 3", "gene_symbol": "[\"Dpysl3\"]", "do": null }, { "gene_id": 22241, "description": "unc-51 like kinase 1", "gene_symbol": "[\"Ulk1\"]", "do": null }, { "gene_id": 22242, "description": "uromodulin", "gene_symbol": "[\"Umod\"]", "do": "[{\"label\":\"autosomal dominant tubulointerstitial kidney disease\",\"id\":\"DOID:0060062\"},{\"label\":\"kidney disease\",\"id\":\"DOID:557\"}]" }, { "gene_id": 22247, "description": "uridine monophosphate synthetase", "gene_symbol": "[\"Umps\"]", "do": null }, { "gene_id": 22253, "description": "unc-5 netrin receptor C", "gene_symbol": "[\"Unc5c\"]", "do": null }, { "gene_id": 22256, "description": "uracil DNA glycosylase", "gene_symbol": "[\"Ung\"]", "do": null }, { "gene_id": 22258, "description": "ubiquitin specific peptidase 4", "gene_symbol": "[\"Usp4\"]", "do": null }, { "gene_id": 22268, "description": "uroplakin 1B", "gene_symbol": "[\"Upk1b\"]", "do": null }, { "gene_id": 22270, "description": "uroplakin 3A", "gene_symbol": "[\"Upk3a\"]", "do": "[{\"label\":\"vesicoureteral reflux\",\"id\":\"DOID:9620\"}]" }, { "gene_id": 22271, "description": "uridine phosphorylase 1", "gene_symbol": "[\"Upp1\"]", "do": null }, { "gene_id": 22273, "description": "ubiquinol-cytochrome c reductase core protein 1", "gene_symbol": "[\"Uqcrc1\"]", "do": null }, { "gene_id": 22278, "description": "upstream transcription factor 1", "gene_symbol": "[\"Usf1\"]", "do": null }, { "gene_id": 22283, "description": "usherin", "gene_symbol": "[\"Ush2a\"]", "do": "[{\"label\":\"Usher syndrome type 2A\",\"id\":\"DOID:0110838\"}]" }, { "gene_id": 22284, "description": "ubiquitin specific peptidase 9, X chromosome", "gene_symbol": "[\"Usp9x\"]", "do": null }, { "gene_id": 22286, "description": "undifferentiated embryonic cell transcription factor 1", "gene_symbol": "[\"Utf1\"]", "do": null }, { "gene_id": 22289, "description": "lysine (K)-specific demethylase 6A", "gene_symbol": "[\"Kdm6a\"]", "do": "[{\"label\":\"chronic myelomonocytic leukemia\",\"id\":\"DOID:0080188\"}]" }, { "gene_id": 22293, "description": "solute carrier family 45, member 2", "gene_symbol": "[\"Slc45a2\"]", "do": "[{\"label\":\"oculocutaneous albinism\",\"id\":\"DOID:0050632\"}]" }, { "gene_id": 22294, "description": "ubiquitously expressed prefoldin like chaperone", "gene_symbol": "[\"Uxt\"]", "do": null }, { "gene_id": 22295, "description": "cadherin related 23 (otocadherin)", "gene_symbol": "[\"Cdh23\"]", "do": "[{\"label\":\"Usher syndrome type 1D\",\"id\":\"DOID:0110831\"},{\"label\":\"autosomal recessive nonsyndromic deafness 12\",\"id\":\"DOID:0110467\"}]" }, { "gene_id": 22296, "description": "vomeronasal 1 receptor 51", "gene_symbol": "[\"Vmn1r51\"]", "do": null }, { "gene_id": 22297, "description": "vomeronasal 1 receptor 45", "gene_symbol": "[\"Vmn1r45\"]", "do": null }, { "gene_id": 22318, "description": "vesicle-associated membrane protein 2", "gene_symbol": "[\"Vamp2\"]", "do": null }, { "gene_id": 22321, "description": "valyl-tRNA synthetase 1", "gene_symbol": "[\"Vars1\"]", "do": null }, { "gene_id": 22329, "description": "vascular cell adhesion molecule 1", "gene_symbol": "[\"Vcam1\"]", "do": null }, { "gene_id": 22330, "description": "vinculin", "gene_symbol": "[\"Vcl\"]", "do": null }, { "gene_id": 22333, "description": "voltage-dependent anion channel 1", "gene_symbol": "[\"Vdac1\"]", "do": null }, { "gene_id": 22334, "description": "voltage-dependent anion channel 2", "gene_symbol": "[\"Vdac2\"]", "do": null }, { "gene_id": 22335, "description": "voltage-dependent anion channel 3", "gene_symbol": "[\"Vdac3\"]", "do": null }, { "gene_id": 22339, "description": "vascular endothelial growth factor A", "gene_symbol": "[\"Vegfa\"]", "do": "[{\"label\":\"DiGeorge syndrome\",\"id\":\"DOID:11198\"},{\"label\":\"amyotrophic lateral sclerosis type 1\",\"id\":\"DOID:0060193\"},{\"label\":\"newborn respiratory distress syndrome\",\"id\":\"DOID:12716\"},{\"label\":\"psoriasis\",\"id\":\"DOID:8893\"}]" }, { "gene_id": 22341, "description": "vascular endothelial growth factor C", "gene_symbol": "[\"Vegfc\"]", "do": "[{\"label\":\"hereditary lymphedema\",\"id\":\"DOID:0050580\"}]" }, { "gene_id": 22344, "description": "vascular endothelial zinc finger 1", "gene_symbol": "[\"Vezf1\"]", "do": null }, { "gene_id": 22348, "description": "solute carrier family 32 (GABA vesicular transporter), member 1", "gene_symbol": "[\"Slc32a1\"]", "do": "[{\"label\":\"temporal lobe epilepsy\",\"id\":\"DOID:3328\"}]" }, { "gene_id": 22352, "description": "vimentin", "gene_symbol": "[\"Vim\"]", "do": "[{\"label\":\"cataract 30\",\"id\":\"DOID:0110248\"}]" }, { "gene_id": 22353, "description": "vasoactive intestinal polypeptide", "gene_symbol": "[\"Vip\"]", "do": "[{\"label\":\"primary pulmonary hypertension\",\"id\":\"DOID:14557\"}]" }, { "gene_id": 22354, "description": "vasoactive intestinal peptide receptor 1", "gene_symbol": "[\"Vipr1\"]", "do": null }, { "gene_id": 22355, "description": "vasoactive intestinal peptide receptor 2", "gene_symbol": "[\"Vipr2\"]", "do": null }, { "gene_id": 22359, "description": "very low density lipoprotein receptor", "gene_symbol": "[\"Vldlr\"]", "do": "[{\"label\":\"age related macular degeneration 1\",\"id\":\"DOID:0110014\"}]" }, { "gene_id": 22360, "description": "neurensin 1", "gene_symbol": "[\"Nrsn1\"]", "do": null }, { "gene_id": 22361, "description": "vanin 1", "gene_symbol": "[\"Vnn1\"]", "do": null }, { "gene_id": 22368, "description": "transient receptor potential cation channel, subfamily V, member 2", "gene_symbol": "[\"Trpv2\"]", "do": null }, { "gene_id": 22370, "description": "vitronectin", "gene_symbol": "[\"Vtn\"]", "do": null }, { "gene_id": 22371, "description": "Von Willebrand factor", "gene_symbol": "[\"Vwf\"]", "do": "[{\"label\":\"von Willebrand's disease 2\",\"id\":\"DOID:0060574\"},{\"label\":\"von Willebrand's disease\",\"id\":\"DOID:12531\"}]" }, { "gene_id": 22378, "description": "WW domain binding protein 2", "gene_symbol": "[\"Wbp2\"]", "do": null }, { "gene_id": 22388, "description": "WD repeat domain 1", "gene_symbol": "[\"Wdr1\"]", "do": null }, { "gene_id": 22393, "description": "wolframin ER transmembrane glycoprotein", "gene_symbol": "[\"Wfs1\"]", "do": "[{\"label\":\"Wolfram syndrome 1\",\"id\":\"DOID:0110629\"},{\"label\":\"nonsyndromic deafness\",\"id\":\"DOID:0050563\"}]" }, { "gene_id": 22402, "description": "cellular communication network factor 4", "gene_symbol": "[\"Ccn4\"]", "do": null }, { "gene_id": 22403, "description": "cellular communication network factor 5", "gene_symbol": "[\"Ccn5\"]", "do": null }, { "gene_id": 22404, "description": "widely-interspaced zinc finger motifs", "gene_symbol": "[\"Wiz\"]", "do": null }, { "gene_id": 22408, "description": "wingless-type MMTV integration site family, member 1", "gene_symbol": "[\"Wnt1\"]", "do": "[{\"label\":\"breast cancer\",\"id\":\"DOID:1612\"}]" }, { "gene_id": 22409, "description": "wingless-type MMTV integration site family, member 10A", "gene_symbol": "[\"Wnt10a\"]", "do": null }, { "gene_id": 22410, "description": "wingless-type MMTV integration site family, member 10B", "gene_symbol": "[\"Wnt10b\"]", "do": null }, { "gene_id": 22411, "description": "wingless-type MMTV integration site family, member 11", "gene_symbol": "[\"Wnt11\"]", "do": null }, { "gene_id": 22412, "description": "wingless-type MMTV integration site family, member 9B", "gene_symbol": "[\"Wnt9b\"]", "do": null }, { "gene_id": 22413, "description": "wingless-type MMTV integration site family, member 2", "gene_symbol": "[\"Wnt2\"]", "do": null }, { "gene_id": 22414, "description": "wingless-type MMTV integration site family, member 2B", "gene_symbol": "[\"Wnt2b\"]", "do": null }, { "gene_id": 22415, "description": "wingless-type MMTV integration site family, member 3", "gene_symbol": "[\"Wnt3\"]", "do": null }, { "gene_id": 22416, "description": "wingless-type MMTV integration site family, member 3A", "gene_symbol": "[\"Wnt3a\"]", "do": null }, { "gene_id": 22417, "description": "wingless-type MMTV integration site family, member 4", "gene_symbol": "[\"Wnt4\"]", "do": null }, { "gene_id": 22418, "description": "wingless-type MMTV integration site family, member 5A", "gene_symbol": "[\"Wnt5a\"]", "do": "[{\"label\":\"Robinow syndrome\",\"id\":\"DOID:0060254\"}]" }, { "gene_id": 22419, "description": "wingless-type MMTV integration site family, member 5B", "gene_symbol": "[\"Wnt5b\"]", "do": null }, { "gene_id": 22420, "description": "wingless-type MMTV integration site family, member 6", "gene_symbol": "[\"Wnt6\"]", "do": null }, { "gene_id": 22421, "description": "wingless-type MMTV integration site family, member 7A", "gene_symbol": "[\"Wnt7a\"]", "do": "[{\"label\":\"Fuhrmann syndrome\",\"id\":\"DOID:0090067\"}]" }, { "gene_id": 22422, "description": "wingless-type MMTV integration site family, member 7B", "gene_symbol": "[\"Wnt7b\"]", "do": null }, { "gene_id": 22423, "description": "wingless-type MMTV integration site family, member 8B", "gene_symbol": "[\"Wnt8b\"]", "do": null }, { "gene_id": 22427, "description": "Werner syndrome RecQ like helicase", "gene_symbol": "[\"Wrn\"]", "do": "[{\"label\":\"Werner syndrome\",\"id\":\"DOID:5688\"}]" }, { "gene_id": 22437, "description": "xin actin-binding repeat containing 1", "gene_symbol": "[\"Xirp1\"]", "do": null }, { "gene_id": 22589, "description": "ATRX, chromatin remodeler", "gene_symbol": "[\"Atrx\"]", "do": "[{\"label\":\"alpha thalassemia-X-linked intellectual disability syndrome\",\"id\":\"DOID:0110030\"}]" }, { "gene_id": 22598, "description": "solute carrier family 6 (neurotransmitter transporter), member 18", "gene_symbol": "[\"Slc6a18\"]", "do": null }, { "gene_id": 22599, "description": "solute carrier family 6 (neurotransmitter transporter), member 20B", "gene_symbol": "[\"Slc6a20b\"]", "do": null }, { "gene_id": 22601, "description": "yes-associated protein 1", "gene_symbol": "[\"Yap1\"]", "do": "[{\"label\":\"cone dystrophy\",\"id\":\"DOID:0050795\"}]" }, { "gene_id": 22612, "description": "YES proto-oncogene 1, Src family tyrosine kinase", "gene_symbol": "[\"Yes1\"]", "do": null }, { "gene_id": 22619, "description": "sialic acid acetylesterase", "gene_symbol": "[\"Siae\"]", "do": null }, { "gene_id": 22625, "description": "mitogen-activated protein kinase kinase kinase 19", "gene_symbol": "[\"Map3k19\"]", "do": null }, { "gene_id": 22627, "description": "tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide", "gene_symbol": "[\"Ywhae\"]", "do": "[{\"label\":\"Miller-Dieker lissencephaly syndrome\",\"id\":\"DOID:0060469\"},{\"label\":\"left ventricular noncompaction\",\"id\":\"DOID:0060480\"}]" }, { "gene_id": 22628, "description": "tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptide", "gene_symbol": "[\"Ywhag\"]", "do": null }, { "gene_id": 22629, "description": "tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, eta polypeptide", "gene_symbol": "[\"Ywhah\"]", "do": null }, { "gene_id": 22630, "description": "tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta", "gene_symbol": "[\"Ywhaq\"]", "do": null }, { "gene_id": 22631, "description": "tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide", "gene_symbol": "[\"Ywhaz\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 22635, "description": "zonadhesin", "gene_symbol": "[\"Zan\"]", "do": null }, { "gene_id": 22661, "description": "zinc finger protein 148", "gene_symbol": "[\"Zfp148\"]", "do": null }, { "gene_id": 22680, "description": "zinc finger protein 207", "gene_symbol": "[\"Zfp207\"]", "do": null }, { "gene_id": 22763, "description": "zinc finger RNA binding protein", "gene_symbol": "[\"Zfr\"]", "do": null }, { "gene_id": 22770, "description": "zinc fingers and homeoboxes 1", "gene_symbol": "[\"Zhx1\"]", "do": null }, { "gene_id": 22773, "description": "zinc finger protein of the cerebellum 3", "gene_symbol": "[\"Zic3\"]", "do": "[{\"label\":\"Goldenhar syndrome\",\"id\":\"DOID:2907\"},{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 22781, "description": "IKAROS family zinc finger 4", "gene_symbol": "[\"Ikzf4\"]", "do": "[{\"label\":\"encephalomyelitis\",\"id\":\"DOID:640\"}]" }, { "gene_id": 22782, "description": "solute carrier family 30 (zinc transporter), member 1", "gene_symbol": "[\"Slc30a1\"]", "do": null }, { "gene_id": 22786, "description": "zona pellucida glycoprotein 1", "gene_symbol": "[\"Zp1\"]", "do": null }, { "gene_id": 22787, "description": "zona pellucida glycoprotein 2", "gene_symbol": "[\"Zp2\"]", "do": null }, { "gene_id": 22788, "description": "zona pellucida glycoprotein 3", "gene_symbol": "[\"Zp3\"]", "do": null }, { "gene_id": 22789, "description": "zona pellucida 3 receptor", "gene_symbol": "[\"Zp3r\"]", "do": null }, { "gene_id": 22793, "description": "zyxin", "gene_symbol": "[\"Zyx\"]", "do": null }, { "gene_id": 23789, "description": "coronin, actin binding protein 1B", "gene_symbol": "[\"Coro1b\"]", "do": null }, { "gene_id": 23792, "description": "a disintegrin and metallopeptidase domain 23", "gene_symbol": "[\"Adam23\"]", "do": null }, { "gene_id": 23793, "description": "ADAM metallopeptidase domain 25", "gene_symbol": "[\"Adam25\"]", "do": null }, { "gene_id": 23794, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 5", "gene_symbol": "[\"Adamts5\"]", "do": null }, { "gene_id": 23796, "description": "apelin receptor", "gene_symbol": "[\"Aplnr\"]", "do": null }, { "gene_id": 23797, "description": "Akt serine/threonine kinase 3", "gene_symbol": "[\"Akt3\"]", "do": null }, { "gene_id": 23821, "description": "beta-site APP cleaving enzyme 1", "gene_symbol": "[\"Bace1\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 23828, "description": "popeye domain cAMP effector 1", "gene_symbol": "[\"Popdc1\"]", "do": null }, { "gene_id": 23831, "description": "carbonic anhydrase 14", "gene_symbol": "[\"Car14\"]", "do": null }, { "gene_id": 23833, "description": "CD52 antigen", "gene_symbol": "[\"Cd52\"]", "do": null }, { "gene_id": 23836, "description": "cadherin 20", "gene_symbol": "[\"Cdh20\"]", "do": null }, { "gene_id": 23844, "description": "chloride channel accessory 1", "gene_symbol": "[\"Clca1\"]", "do": null }, { "gene_id": 23845, "description": "C-type lectin domain family 5, member a", "gene_symbol": "[\"Clec5a\"]", "do": null }, { "gene_id": 23853, "description": "differentially expressed in FDCP 6", "gene_symbol": "[\"Def6\"]", "do": "[{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 23856, "description": "death inducer-obliterator 1", "gene_symbol": "[\"Dido1\"]", "do": "[{\"label\":\"myelodysplastic/myeloproliferative neoplasm\",\"id\":\"DOID:4972\"}]" }, { "gene_id": 23859, "description": "discs large MAGUK scaffold protein 2", "gene_symbol": "[\"Dlg2\"]", "do": null }, { "gene_id": 23863, "description": "DAN domain family member 5, BMP antagonist", "gene_symbol": "[\"Dand5\"]", "do": null }, { "gene_id": 23876, "description": "fibulin 5", "gene_symbol": "[\"Fbln5\"]", "do": "[{\"label\":\"cutis laxa\",\"id\":\"DOID:3144\"}]" }, { "gene_id": 23881, "description": "G3BP stress granule assembly factor 2", "gene_symbol": "[\"G3bp2\"]", "do": null }, { "gene_id": 23886, "description": "growth differentiation factor 15", "gene_symbol": "[\"Gdf15\"]", "do": null }, { "gene_id": 23887, "description": "gamma-glutamyltransferase 5", "gene_symbol": "[\"Ggt5\"]", "do": null }, { "gene_id": 23890, "description": "G protein-coupled receptor 34", "gene_symbol": "[\"Gpr34\"]", "do": null }, { "gene_id": 23892, "description": "gremlin 1, DAN family BMP antagonist", "gene_symbol": "[\"Grem1\"]", "do": null }, { "gene_id": 23893, "description": "gremlin 2, DAN family BMP antagonist", "gene_symbol": "[\"Grem2\"]", "do": null }, { "gene_id": 23908, "description": "heparan sulfate 2-O-sulfotransferase 1", "gene_symbol": "[\"Hs2st1\"]", "do": null }, { "gene_id": 23920, "description": "insulin receptor-related receptor", "gene_symbol": "[\"Insrr\"]", "do": null }, { "gene_id": 23925, "description": "Kell blood group", "gene_symbol": "[\"Kel\"]", "do": null }, { "gene_id": 23928, "description": "laminin gamma 3", "gene_symbol": "[\"Lamc3\"]", "do": null }, { "gene_id": 23934, "description": "lymphocyte antigen 6 family member H", "gene_symbol": "[\"Ly6h\"]", "do": null }, { "gene_id": 23948, "description": "matrix metallopeptidase 17", "gene_symbol": "[\"Mmp17\"]", "do": null }, { "gene_id": 23955, "description": "NIMA (never in mitosis gene a)-related expressed kinase 4", "gene_symbol": "[\"Nek4\"]", "do": null }, { "gene_id": 23956, "description": "neuraminidase 2", "gene_symbol": "[\"Neu2\"]", "do": null }, { "gene_id": 23959, "description": "5' nucleotidase, ecto", "gene_symbol": "[\"Nt5e\"]", "do": null }, { "gene_id": 23961, "description": "2'-5' oligoadenylate synthetase 1B", "gene_symbol": "[\"Oas1b\"]", "do": null }, { "gene_id": 23963, "description": "teneurin transmembrane protein 1", "gene_symbol": "[\"Tenm1\"]", "do": null }, { "gene_id": 23964, "description": "teneurin transmembrane protein 2", "gene_symbol": "[\"Tenm2\"]", "do": null }, { "gene_id": 23965, "description": "teneurin transmembrane protein 3", "gene_symbol": "[\"Tenm3\"]", "do": null }, { "gene_id": 23966, "description": "teneurin transmembrane protein 4", "gene_symbol": "[\"Tenm4\"]", "do": null }, { "gene_id": 23969, "description": "protein kinase C and casein kinase substrate in neurons 1", "gene_symbol": "[\"Pacsin1\"]", "do": null }, { "gene_id": 23970, "description": "protein kinase C and casein kinase substrate in neurons 2", "gene_symbol": "[\"Pacsin2\"]", "do": null }, { "gene_id": 23983, "description": "poly(rC) binding protein 1", "gene_symbol": "[\"Pcbp1\"]", "do": null }, { "gene_id": 23984, "description": "phosphodiesterase 10A", "gene_symbol": "[\"Pde10a\"]", "do": null }, { "gene_id": 23992, "description": "protein kinase, interferon inducible double stranded RNA dependent activator", "gene_symbol": "[\"Prkra\"]", "do": null }, { "gene_id": 24001, "description": "T cell lymphoma invasion and metastasis 2", "gene_symbol": "[\"Tiam2\"]", "do": null }, { "gene_id": 24012, "description": "regulator of G protein signaling 7", "gene_symbol": "[\"Rgs7\"]", "do": null }, { "gene_id": 24015, "description": "ATP-binding cassette, sub-family E member 1", "gene_symbol": "[\"Abce1\"]", "do": null }, { "gene_id": 24017, "description": "ring finger protein 13", "gene_symbol": "[\"Rnf13\"]", "do": null }, { "gene_id": 24046, "description": "sodium channel, voltage-gated, type XI, alpha", "gene_symbol": "[\"Scn11a\"]", "do": "[{\"label\":\"familial episodic pain syndrome 3\",\"id\":\"DOID:0111731\"},{\"label\":\"hereditary sensory and autonomic neuropathy\",\"id\":\"DOID:0050548\"}]" }, { "gene_id": 24047, "description": "C-C motif chemokine ligand 19", "gene_symbol": "[\"Ccl19\"]", "do": null }, { "gene_id": 24051, "description": "sarcoglycan, beta (dystrophin-associated glycoprotein)", "gene_symbol": "[\"Sgcb\"]", "do": "[{\"label\":\"autosomal recessive limb-girdle muscular dystrophy type 2E\",\"id\":\"DOID:0110279\"}]" }, { "gene_id": 24052, "description": "sarcoglycan, delta (dystrophin-associated glycoprotein)", "gene_symbol": "[\"Sgcd\"]", "do": "[{\"label\":\"autosomal recessive limb-girdle muscular dystrophy type 2F\",\"id\":\"DOID:0110280\"},{\"label\":\"dilated cardiomyopathy 1L\",\"id\":\"DOID:0110436\"}]" }, { "gene_id": 24053, "description": "sarcoglycan, gamma (dystrophin-associated glycoprotein)", "gene_symbol": "[\"Sgcg\"]", "do": "[{\"label\":\"autosomal recessive limb-girdle muscular dystrophy type 2C\",\"id\":\"DOID:0110277\"},{\"label\":\"limb-girdle muscular dystrophy\",\"id\":\"DOID:11724\"}]" }, { "gene_id": 24058, "description": "single immunoglobulin and toll-interleukin 1 receptor (TIR) domain", "gene_symbol": "[\"Sigirr\"]", "do": null }, { "gene_id": 24059, "description": "solute carrier organic anion transporter family, member 2a1", "gene_symbol": "[\"Slco2a1\"]", "do": null }, { "gene_id": 24064, "description": "sprouty RTK signaling antagonist 2", "gene_symbol": "[\"Spry2\"]", "do": "[{\"label\":\"achalasia\",\"id\":\"DOID:9164\"},{\"label\":\"ciliopathy\",\"id\":\"DOID:0060340\"},{\"label\":\"intestinal pseudo-obstruction\",\"id\":\"DOID:0080072\"}]" }, { "gene_id": 24068, "description": "steroid receptor RNA activator 1", "gene_symbol": "[\"Sra1\"]", "do": null }, { "gene_id": 24070, "description": "mannose-P-dolichol utilization defect 1", "gene_symbol": "[\"Mpdu1\"]", "do": null }, { "gene_id": 24074, "description": "TATA-box binding protein associated factor 7", "gene_symbol": "[\"Taf7\"]", "do": null }, { "gene_id": 24087, "description": "tolloid-like 2", "gene_symbol": "[\"Tll2\"]", "do": null }, { "gene_id": 24088, "description": "toll-like receptor 2", "gene_symbol": "[\"Tlr2\"]", "do": null }, { "gene_id": 24099, "description": "tumor necrosis factor (ligand) superfamily, member 13b", "gene_symbol": "[\"Tnfsf13b\"]", "do": "[{\"label\":\"IgA glomerulonephritis\",\"id\":\"DOID:2986\"},{\"label\":\"Sjogren's syndrome\",\"id\":\"DOID:12894\"}]" }, { "gene_id": 24100, "description": "transmembrane protein, adipocyte asscociated 1", "gene_symbol": "[\"Tpra1\"]", "do": null }, { "gene_id": 24112, "description": "vomeronasal 1, receptor 49", "gene_symbol": "[\"Vmn1r49\"]", "do": null }, { "gene_id": 24116, "description": "negative elongation factor complex member A, Whsc2", "gene_symbol": "[\"Nelfa\"]", "do": null }, { "gene_id": 24117, "description": "Wnt inhibitory factor 1", "gene_symbol": "[\"Wif1\"]", "do": null }, { "gene_id": 24128, "description": "5'-3' exoribonuclease 2", "gene_symbol": "[\"Xrn2\"]", "do": null }, { "gene_id": 24131, "description": "LIM domain binding 3", "gene_symbol": "[\"Ldb3\"]", "do": "[{\"label\":\"congenital myopathy\",\"id\":\"DOID:0081337\"},{\"label\":\"dilated cardiomyopathy 1C\",\"id\":\"DOID:0110423\"},{\"label\":\"myofibrillar myopathy 1\",\"id\":\"DOID:0080092\"}]" }, { "gene_id": 24136, "description": "zinc finger E-box binding homeobox 2", "gene_symbol": "[\"Zeb2\"]", "do": "[{\"label\":\"Mowat-Wilson syndrome\",\"id\":\"DOID:0060485\"},{\"label\":\"T-cell adult acute lymphocytic leukemia\",\"id\":\"DOID:5602\"}]" }, { "gene_id": 26356, "description": "inhibitor of growth family, member 1", "gene_symbol": "[\"Ing1\"]", "do": null }, { "gene_id": 26357, "description": "ATP binding cassette subfamily G member 2 (Junior blood group)", "gene_symbol": "[\"Abcg2\"]", "do": "[{\"label\":\"erythropoietic protoporphyria\",\"id\":\"DOID:13270\"},{\"label\":\"hyperuricemia\",\"id\":\"DOID:1920\"}]" }, { "gene_id": 26358, "description": "aldehyde dehydrogenase family 1, subfamily A7", "gene_symbol": "[\"Aldh1a7\"]", "do": null }, { "gene_id": 26360, "description": "angiopoietin-like 2", "gene_symbol": "[\"Angptl2\"]", "do": "[{\"label\":\"dermatomyositis\",\"id\":\"DOID:10223\"}]" }, { "gene_id": 26361, "description": "arginine vasopressin receptor 1B", "gene_symbol": "[\"Avpr1b\"]", "do": null }, { "gene_id": 26362, "description": "AXL receptor tyrosine kinase", "gene_symbol": "[\"Axl\"]", "do": null }, { "gene_id": 26363, "description": "biotinidase", "gene_symbol": "[\"Btd\"]", "do": "[{\"label\":\"biotinidase deficiency\",\"id\":\"DOID:856\"}]" }, { "gene_id": 26364, "description": "adhesion G protein-coupled receptor E5", "gene_symbol": "[\"Adgre5\"]", "do": null }, { "gene_id": 26365, "description": "CEA cell adhesion molecule 1", "gene_symbol": "[\"Ceacam1\"]", "do": null }, { "gene_id": 26366, "description": "CEA cell adhesion molecule 10", "gene_symbol": "[\"Ceacam10\"]", "do": null }, { "gene_id": 26367, "description": "CEA cell adhesion molecule 2", "gene_symbol": "[\"Ceacam2\"]", "do": null }, { "gene_id": 26372, "description": "chloride channel, voltage-sensitive 6", "gene_symbol": "[\"Clcn6\"]", "do": "[{\"label\":\"neuronal ceroid lipofuscinosis 3\",\"id\":\"DOID:0110731\"}]" }, { "gene_id": 26378, "description": "2-4-dienoyl-Coenzyme A reductase 2, peroxisomal", "gene_symbol": "[\"Decr2\"]", "do": null }, { "gene_id": 26380, "description": "estrogen related receptor, beta", "gene_symbol": "[\"Esrrb\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 26381, "description": "estrogen-related receptor gamma", "gene_symbol": "[\"Esrrg\"]", "do": null }, { "gene_id": 26383, "description": "FTO alpha-ketoglutarate dependent dioxygenase", "gene_symbol": "[\"Fto\"]", "do": null }, { "gene_id": 26384, "description": "glucosamine-6-phosphate deaminase 1", "gene_symbol": "[\"Gnpda1\"]", "do": null }, { "gene_id": 26394, "description": "lysophospholipase 2", "gene_symbol": "[\"Lypla2\"]", "do": null }, { "gene_id": 26395, "description": "mitogen-activated protein kinase kinase 1", "gene_symbol": "[\"Map2k1\"]", "do": "[{\"label\":\"cardiofaciocutaneous syndrome\",\"id\":\"DOID:0060233\"}]" }, { "gene_id": 26397, "description": "mitogen-activated protein kinase kinase 3", "gene_symbol": "[\"Map2k3\"]", "do": null }, { "gene_id": 26398, "description": "mitogen-activated protein kinase kinase 4", "gene_symbol": "[\"Map2k4\"]", "do": null }, { "gene_id": 26408, "description": "mitogen-activated protein kinase kinase kinase 5", "gene_symbol": "[\"Map3k5\"]", "do": null }, { "gene_id": 26409, "description": "mitogen-activated protein kinase kinase kinase 7", "gene_symbol": "[\"Map3k7\"]", "do": "[{\"label\":\"Wolff-Parkinson-White syndrome\",\"id\":\"DOID:384\"}]" }, { "gene_id": 26416, "description": "mitogen-activated protein kinase 14", "gene_symbol": "[\"Mapk14\"]", "do": null }, { "gene_id": 26421, "description": "prolactin family 2, subfamily c, member 4", "gene_symbol": "[\"Prl2c4\"]", "do": null }, { "gene_id": 26422, "description": "neurobeachin", "gene_symbol": "[\"Nbea\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 26427, "description": "cAMP responsive element binding protein 3-like 1", "gene_symbol": "[\"Creb3l1\"]", "do": null }, { "gene_id": 26431, "description": "GIT ArfGAP 2", "gene_symbol": "[\"Git2\"]", "do": null }, { "gene_id": 26432, "description": "procollagen lysine, 2-oxoglutarate 5-dioxygenase 2", "gene_symbol": "[\"Plod2\"]", "do": null }, { "gene_id": 26433, "description": "procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3", "gene_symbol": "[\"Plod3\"]", "do": null }, { "gene_id": 26434, "description": "prion like protein doppel", "gene_symbol": "[\"Prnd\"]", "do": null }, { "gene_id": 26436, "description": "pregnancy specific beta-1-glycoprotein 16", "gene_symbol": "[\"Psg16\"]", "do": null }, { "gene_id": 26440, "description": "proteasome subunit alpha 1", "gene_symbol": "[\"Psma1\"]", "do": null }, { "gene_id": 26442, "description": "proteasome subunit alpha 5", "gene_symbol": "[\"Psma5\"]", "do": null }, { "gene_id": 26443, "description": "proteasome subunit alpha 6", "gene_symbol": "[\"Psma6\"]", "do": null }, { "gene_id": 26444, "description": "proteasome subunit alpha 7", "gene_symbol": "[\"Psma7\"]", "do": null }, { "gene_id": 26456, "description": "sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G", "gene_symbol": "[\"Sema4g\"]", "do": null }, { "gene_id": 26458, "description": "solute carrier family 27 (fatty acid transporter), member 2", "gene_symbol": "[\"Slc27a2\"]", "do": null }, { "gene_id": 26459, "description": "solute carrier family 27 (fatty acid transporter), member 5", "gene_symbol": "[\"Slc27a5\"]", "do": null }, { "gene_id": 26464, "description": "vanin 3", "gene_symbol": "[\"Vnn3\"]", "do": null }, { "gene_id": 26554, "description": "cullin 3", "gene_symbol": "[\"Cul3\"]", "do": null }, { "gene_id": 26556, "description": "homer scaffolding protein 1", "gene_symbol": "[\"Homer1\"]", "do": null }, { "gene_id": 26561, "description": "matrix metallopeptidase 23", "gene_symbol": "[\"Mmp23\"]", "do": null }, { "gene_id": 26562, "description": "neurochondrin", "gene_symbol": "[\"Ncdn\"]", "do": null }, { "gene_id": 26563, "description": "receptor tyrosine kinase-like orphan receptor 1", "gene_symbol": "[\"Ror1\"]", "do": null }, { "gene_id": 26564, "description": "receptor tyrosine kinase-like orphan receptor 2", "gene_symbol": "[\"Ror2\"]", "do": "[{\"label\":\"autosomal recessive Robinow syndrome\",\"id\":\"DOID:0060764\"}]" }, { "gene_id": 26874, "description": "ATP-binding cassette, sub-family D member 2", "gene_symbol": "[\"Abcd2\"]", "do": null }, { "gene_id": 26875, "description": "piccolo (presynaptic cytomatrix protein)", "gene_symbol": "[\"Pclo\"]", "do": null }, { "gene_id": 26877, "description": "UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 1", "gene_symbol": "[\"B3galt1\"]", "do": null }, { "gene_id": 26878, "description": "UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2", "gene_symbol": "[\"B3galt2\"]", "do": null }, { "gene_id": 26879, "description": "UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 1", "gene_symbol": "[\"B3galnt1\"]", "do": null }, { "gene_id": 26885, "description": "caspase 8 associated protein 2", "gene_symbol": "[\"Casp8ap2\"]", "do": null }, { "gene_id": 26887, "description": "carbohydrate sulfotransferase 4", "gene_symbol": "[\"Chst4\"]", "do": null }, { "gene_id": 26888, "description": "C-type lectin domain family 4, member a2", "gene_symbol": "[\"Clec4a2\"]", "do": null }, { "gene_id": 26898, "description": "cathepsin J", "gene_symbol": "[\"Ctsj\"]", "do": null }, { "gene_id": 26900, "description": "DEAD box helicase 3, Y-linked", "gene_symbol": "[\"Ddx3y\"]", "do": null }, { "gene_id": 26901, "description": "SS18, nBAF chromatin remodeling complex subunit like 2", "gene_symbol": "[\"Ss18l2\"]", "do": null }, { "gene_id": 26903, "description": "dysferlin", "gene_symbol": "[\"Dysf\"]", "do": "[{\"label\":\"autosomal recessive limb-girdle muscular dystrophy type 2B\",\"id\":\"DOID:0110276\"},{\"label\":\"distal myopathy\",\"id\":\"DOID:11720\"}]" }, { "gene_id": 26905, "description": "eukaryotic translation initiation factor 2, subunit 3, structural gene X-linked", "gene_symbol": "[\"Eif2s3x\"]", "do": null }, { "gene_id": 26913, "description": "G protein-regulated inducer of neurite outgrowth 1", "gene_symbol": "[\"Gprin1\"]", "do": null }, { "gene_id": 26918, "description": "endoplasmic reticulum to nucleus signalling 2", "gene_symbol": "[\"Ern2\"]", "do": null }, { "gene_id": 26920, "description": "centriolin", "gene_symbol": "[\"Cntrl\"]", "do": null }, { "gene_id": 26921, "description": "mitogen-activated protein kinase kinase kinase kinase 4", "gene_symbol": "[\"Map4k4\"]", "do": null }, { "gene_id": 26926, "description": "apoptosis-inducing factor, mitochondrion-associated 1", "gene_symbol": "[\"Aifm1\"]", "do": "[{\"label\":\"mitochondrial complex I deficiency\",\"id\":\"DOID:0060536\"}]" }, { "gene_id": 26934, "description": "Rac GTPase-activating protein 1", "gene_symbol": "[\"Racgap1\"]", "do": null }, { "gene_id": 26936, "description": "myosin phosphatase Rho interacting protein", "gene_symbol": "[\"Mprip\"]", "do": null }, { "gene_id": 26938, "description": "ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 5", "gene_symbol": "[\"St6galnac5\"]", "do": null }, { "gene_id": 26943, "description": "serine incorporator 3", "gene_symbol": "[\"Serinc3\"]", "do": null }, { "gene_id": 26944, "description": "tubulointerstitial nephritis antigen", "gene_symbol": "[\"Tinag\"]", "do": null }, { "gene_id": 26946, "description": "transient receptor potential cation channel, subfamily C, member 7", "gene_symbol": "[\"Trpc7\"]", "do": null }, { "gene_id": 26949, "description": "vesicle amine transport 1", "gene_symbol": "[\"Vat1\"]", "do": null }, { "gene_id": 26951, "description": "zw10 kinetochore protein", "gene_symbol": "[\"Zw10\"]", "do": null }, { "gene_id": 26968, "description": "immunoglobulin superfamily containing leucine-rich repeat", "gene_symbol": "[\"Islr\"]", "do": null }, { "gene_id": 26971, "description": "phospholipase A2, group IIF", "gene_symbol": "[\"Pla2g2f\"]", "do": null }, { "gene_id": 27007, "description": "killer cell lectin-like receptor subfamily K, member 1", "gene_symbol": "[\"Klrk1\"]", "do": null }, { "gene_id": 27028, "description": "erythroblast membrane-associated protein", "gene_symbol": "[\"Ermap\"]", "do": null }, { "gene_id": 27029, "description": "N-sulfoglucosamine sulfohydrolase (sulfamidase)", "gene_symbol": "[\"Sgsh\"]", "do": "[{\"label\":\"mucopolysaccharidosis III\",\"id\":\"DOID:12801\"}]" }, { "gene_id": 27041, "description": "G3BP stress granule assembly factor 1", "gene_symbol": "[\"G3bp1\"]", "do": null }, { "gene_id": 27047, "description": "osteomodulin", "gene_symbol": "[\"Omd\"]", "do": null }, { "gene_id": 27050, "description": "ribosomal protein S3", "gene_symbol": "[\"Rps3\"]", "do": null }, { "gene_id": 27052, "description": "acyloxyacyl hydrolase", "gene_symbol": "[\"Aoah\"]", "do": null }, { "gene_id": 27054, "description": "SEC23 homolog B, COPII coat complex component", "gene_symbol": "[\"Sec23b\"]", "do": null }, { "gene_id": 27055, "description": "FK506 binding protein 9", "gene_symbol": "[\"Fkbp9\"]", "do": null }, { "gene_id": 27056, "description": "interferon regulatory factor 5", "gene_symbol": "[\"Irf5\"]", "do": null }, { "gene_id": 27059, "description": "SH3 domain protein D19", "gene_symbol": "[\"Sh3d19\"]", "do": null }, { "gene_id": 27062, "description": "Ca2+-dependent secretion activator", "gene_symbol": "[\"Cadps\"]", "do": null }, { "gene_id": 27176, "description": "ribosomal protein L7A", "gene_symbol": "[\"Rpl7a\"]", "do": null }, { "gene_id": 27205, "description": "podocalyxin-like", "gene_symbol": "[\"Podxl\"]", "do": null }, { "gene_id": 27206, "description": "Nik related kinase", "gene_symbol": "[\"Nrk\"]", "do": null }, { "gene_id": 27216, "description": "olfactory receptor family 5 subfamily G member 26", "gene_symbol": "[\"Or5g26\"]", "do": null }, { "gene_id": 27218, "description": "signaling lymphocytic activation molecule family member 1", "gene_symbol": "[\"Slamf1\"]", "do": null }, { "gene_id": 27220, "description": "CART prepropeptide", "gene_symbol": "[\"Cartpt\"]", "do": null }, { "gene_id": 27221, "description": "chromatin assembly factor 1, subunit A", "gene_symbol": "[\"Chaf1a\"]", "do": null }, { "gene_id": 27223, "description": "transformation related protein 53 binding protein 1", "gene_symbol": "[\"Trp53bp1\"]", "do": null }, { "gene_id": 27226, "description": "phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma)", "gene_symbol": "[\"Pla2g7\"]", "do": null }, { "gene_id": 27277, "description": "golgin A5", "gene_symbol": "[\"Golga5\"]", "do": null }, { "gene_id": 27357, "description": "glycogenin 1", "gene_symbol": "[\"Gyg1\"]", "do": "[{\"label\":\"glycogen storage disease XV\",\"id\":\"DOID:0050579\"}]" }, { "gene_id": 27364, "description": "serine racemase", "gene_symbol": "[\"Srr\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 27370, "description": "ribosomal protein S26", "gene_symbol": "[\"Rps26\"]", "do": null }, { "gene_id": 27372, "description": "prolactin family 3, subfamily c, member 1", "gene_symbol": "[\"Prl3c1\"]", "do": "[{\"label\":\"hyperandrogenism\",\"id\":\"DOID:11613\"}]" }, { "gene_id": 27374, "description": "protein arginine N-methyltransferase 5", "gene_symbol": "[\"Prmt5\"]", "do": null }, { "gene_id": 27376, "description": "solute carrier family 25 (mitochondrial carrier, dicarboxylate transporter), member 10", "gene_symbol": "[\"Slc25a10\"]", "do": null }, { "gene_id": 27385, "description": "MAGE family member L2", "gene_symbol": "[\"Magel2\"]", "do": null }, { "gene_id": 27387, "description": "SH2 domain containing 3C", "gene_symbol": "[\"Sh2d3c\"]", "do": null }, { "gene_id": 27388, "description": "phosphatidylserine synthase 2", "gene_symbol": "[\"Ptdss2\"]", "do": null }, { "gene_id": 27390, "description": "membrane metalloendopeptidase like 1", "gene_symbol": "[\"Mmel1\"]", "do": null }, { "gene_id": 27400, "description": "hydroxysteroid (17-beta) dehydrogenase 6", "gene_symbol": "[\"Hsd17b6\"]", "do": null }, { "gene_id": 27402, "description": "pyruvate dehydrogenase complex, component X", "gene_symbol": "[\"Pdhx\"]", "do": null }, { "gene_id": 27403, "description": "ATP-binding cassette, sub-family A member 7", "gene_symbol": "[\"Abca7\"]", "do": null }, { "gene_id": 27404, "description": "ATP-binding cassette, sub-family A member 8b", "gene_symbol": "[\"Abca8b\"]", "do": null }, { "gene_id": 27406, "description": "ATP-binding cassette, sub-family F member 3", "gene_symbol": "[\"Abcf3\"]", "do": null }, { "gene_id": 27409, "description": "ATP binding cassette subfamily G member 5", "gene_symbol": "[\"Abcg5\"]", "do": null }, { "gene_id": 27410, "description": "ATP-binding cassette, sub-family A member 3", "gene_symbol": "[\"Abca3\"]", "do": "[{\"label\":\"pulmonary alveolar proteinosis\",\"id\":\"DOID:12120\"}]" }, { "gene_id": 27411, "description": "solute carrier family 14 (urea transporter), member 2", "gene_symbol": "[\"Slc14a2\"]", "do": null }, { "gene_id": 27413, "description": "ATP-binding cassette, sub-family B member 11", "gene_symbol": "[\"Abcb11\"]", "do": null }, { "gene_id": 27416, "description": "ATP-binding cassette, sub-family C member 5", "gene_symbol": "[\"Abcc5\"]", "do": null }, { "gene_id": 27419, "description": "alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB)", "gene_symbol": "[\"Naglu\"]", "do": "[{\"label\":\"mucopolysaccharidosis III\",\"id\":\"DOID:12801\"},{\"label\":\"otitis media\",\"id\":\"DOID:10754\"}]" }, { "gene_id": 27421, "description": "ATP-binding cassette, sub-family C member 6", "gene_symbol": "[\"Abcc6\"]", "do": "[{\"label\":\"pseudoxanthoma elasticum\",\"id\":\"DOID:2738\"}]" }, { "gene_id": 27425, "description": "ATP synthase membrane subunit g", "gene_symbol": "[\"Atp5mg\"]", "do": null }, { "gene_id": 27426, "description": "N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase", "gene_symbol": "[\"Nagpa\"]", "do": null }, { "gene_id": 27428, "description": "shroom family member 3", "gene_symbol": "[\"Shroom3\"]", "do": null }, { "gene_id": 27494, "description": "angiomotin", "gene_symbol": "[\"Amot\"]", "do": null }, { "gene_id": 27632, "description": "negative elongation factor complex member E, Rdbp", "gene_symbol": "[\"Nelfe\"]", "do": null }, { "gene_id": 27762, "description": "von Willebrand factor A domain containing 7", "gene_symbol": "[\"Vwa7\"]", "do": null }, { "gene_id": 27801, "description": "zinc finger, DHHC domain containing 8", "gene_symbol": "[\"Zdhhc8\"]", "do": null }, { "gene_id": 27886, "description": "ess-2 splicing factor", "gene_symbol": "[\"Ess2\"]", "do": null }, { "gene_id": 27967, "description": "calcium homeostasis endoplasmic reticulum protein", "gene_symbol": "[\"Cherp\"]", "do": null }, { "gene_id": 27979, "description": "eukaryotic translation initiation factor 3, subunit B", "gene_symbol": "[\"Eif3b\"]", "do": null }, { "gene_id": 28000, "description": "pre-mRNA processing factor 19", "gene_symbol": "[\"Prpf19\"]", "do": null }, { "gene_id": 28006, "description": "WASH complex subunit 2", "gene_symbol": "[\"Washc2\"]", "do": null }, { "gene_id": 28035, "description": "ubiquitin specific peptidase 39", "gene_symbol": "[\"Usp39\"]", "do": null }, { "gene_id": 28064, "description": "Yip1 domain family, member 3", "gene_symbol": "[\"Yipf3\"]", "do": null }, { "gene_id": 28078, "description": "prolactin family 5, subfamily a, member 1", "gene_symbol": "[\"Prl5a1\"]", "do": null }, { "gene_id": 28109, "description": "NOP protein chaperone 1", "gene_symbol": "[\"Nopchap1\"]", "do": null }, { "gene_id": 28146, "description": "stress-associated endoplasmic reticulum protein 1", "gene_symbol": "[\"Serp1\"]", "do": null }, { "gene_id": 28185, "description": "translocase of outer mitochondrial membrane 70A", "gene_symbol": "[\"Tomm70a\"]", "do": null }, { "gene_id": 28194, "description": "apolipoprotein N", "gene_symbol": "[\"Apon\"]", "do": null }, { "gene_id": 28200, "description": "dehydrogenase/reductase 4", "gene_symbol": "[\"Dhrs4\"]", "do": null }, { "gene_id": 28248, "description": "solute carrier organic anion transporter family, member 1a1", "gene_symbol": "[\"Slco1a1\"]", "do": null }, { "gene_id": 28250, "description": "solute carrier organic anion transporter family, member 1a4", "gene_symbol": "[\"Slco1a4\"]", "do": null }, { "gene_id": 28253, "description": "solute carrier organic anion transporter family, member 1b2", "gene_symbol": "[\"Slco1b2\"]", "do": null }, { "gene_id": 28254, "description": "solute carrier organic anion transporter family, member 1a6", "gene_symbol": "[\"Slco1a6\"]", "do": null }, { "gene_id": 29806, "description": "LIM domains containing 1", "gene_symbol": "[\"Limd1\"]", "do": null }, { "gene_id": 29808, "description": "MAX gene associated", "gene_symbol": "[\"Mga\"]", "do": null }, { "gene_id": 29810, "description": "BCL2-associated athanogene 3", "gene_symbol": "[\"Bag3\"]", "do": "[{\"label\":\"dilated cardiomyopathy 1HH\",\"id\":\"DOID:0110448\"}]" }, { "gene_id": 29811, "description": "N-myc downstream regulated gene 2", "gene_symbol": "[\"Ndrg2\"]", "do": null }, { "gene_id": 29812, "description": "N-myc downstream regulated gene 3", "gene_symbol": "[\"Ndrg3\"]", "do": null }, { "gene_id": 29817, "description": "insulin-like growth factor binding protein 7", "gene_symbol": "[\"Igfbp7\"]", "do": null }, { "gene_id": 29819, "description": "staufen double-stranded RNA binding protein 2", "gene_symbol": "[\"Stau2\"]", "do": null }, { "gene_id": 29820, "description": "tumor necrosis factor receptor superfamily, member 19", "gene_symbol": "[\"Tnfrsf19\"]", "do": null }, { "gene_id": 29856, "description": "smoothelin", "gene_symbol": "[\"Smtn\"]", "do": null }, { "gene_id": 29858, "description": "phosphomannomutase 1", "gene_symbol": "[\"Pmm1\"]", "do": null }, { "gene_id": 29869, "description": "unc-51 like kinase 2", "gene_symbol": "[\"Ulk2\"]", "do": null }, { "gene_id": 29873, "description": "chondroitin sulfate proteoglycan 5", "gene_symbol": "[\"Cspg5\"]", "do": null }, { "gene_id": 29875, "description": "IQ motif containing GTPase activating protein 1", "gene_symbol": "[\"Iqgap1\"]", "do": null }, { "gene_id": 30044, "description": "opsin 4 (melanopsin)", "gene_symbol": "[\"Opn4\"]", "do": null }, { "gene_id": 30046, "description": "zinc finger protein 292", "gene_symbol": "[\"Zfp292\"]", "do": null }, { "gene_id": 30052, "description": "proprotein convertase subtilisin/kexin type 1 inhibitor", "gene_symbol": "[\"Pcsk1n\"]", "do": null }, { "gene_id": 30059, "description": "translocase of inner mitochondrial membrane 10", "gene_symbol": "[\"Timm10\"]", "do": null }, { "gene_id": 30060, "description": "melanotransferrin", "gene_symbol": "[\"Meltf\"]", "do": null }, { "gene_id": 30785, "description": "cortactin binding protein 2", "gene_symbol": "[\"Cttnbp2\"]", "do": null }, { "gene_id": 30805, "description": "solute carrier family 22 (organic cation transporter), member 4", "gene_symbol": "[\"Slc22a4\"]", "do": null }, { "gene_id": 30924, "description": "angiopoietin-like 3", "gene_symbol": "[\"Angptl3\"]", "do": null }, { "gene_id": 30925, "description": "SLAM family member 6", "gene_symbol": "[\"Slamf6\"]", "do": null }, { "gene_id": 30930, "description": "VPS26 retromer complex component A", "gene_symbol": "[\"Vps26a\"]", "do": null }, { "gene_id": 30931, "description": "torsin family 1, member A (torsin A)", "gene_symbol": "[\"Tor1a\"]", "do": "[{\"label\":\"focal dystonia\",\"id\":\"DOID:0050836\"},{\"label\":\"torsion dystonia 1\",\"id\":\"DOID:0060730\"}]" }, { "gene_id": 30933, "description": "torsin family 2, member A", "gene_symbol": "[\"Tor2a\"]", "do": null }, { "gene_id": 30934, "description": "torsin family 1, member B", "gene_symbol": "[\"Tor1b\"]", "do": null }, { "gene_id": 30935, "description": "torsin family 3, member A", "gene_symbol": "[\"Tor3a\"]", "do": null }, { "gene_id": 30936, "description": "solute carrier family 46, member 2", "gene_symbol": "[\"Slc46a2\"]", "do": null }, { "gene_id": 30937, "description": "LIM and cysteine-rich domains 1", "gene_symbol": "[\"Lmcd1\"]", "do": null }, { "gene_id": 30943, "description": "serine protease 30", "gene_symbol": "[\"Prss30\"]", "do": null }, { "gene_id": 30956, "description": "aminoadipate-semialdehyde synthase", "gene_symbol": "[\"Aass\"]", "do": null }, { "gene_id": 30957, "description": "mitogen-activated protein kinase 8 interacting protein 3", "gene_symbol": "[\"Mapk8ip3\"]", "do": null }, { "gene_id": 30960, "description": "vesicle-associated membrane protein, associated protein A", "gene_symbol": "[\"Vapa\"]", "do": null }, { "gene_id": 30963, "description": "3-hydroxyacyl-CoA dehydratase 1", "gene_symbol": "[\"Hacd1\"]", "do": null }, { "gene_id": 50490, "description": "NADPH oxidase 4", "gene_symbol": "[\"Nox4\"]", "do": null }, { "gene_id": 50492, "description": "thimet oligopeptidase 1", "gene_symbol": "[\"Thop1\"]", "do": null }, { "gene_id": 50493, "description": "thioredoxin reductase 1", "gene_symbol": "[\"Txnrd1\"]", "do": null }, { "gene_id": 50498, "description": "Epstein-Barr virus induced gene 3", "gene_symbol": "[\"Ebi3\"]", "do": null }, { "gene_id": 50518, "description": "nonagouti", "gene_symbol": "[\"a\"]", "do": "[{\"label\":\"obesity\",\"id\":\"DOID:9970\"},{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 50524, "description": "spalt like transcription factor 2", "gene_symbol": "[\"Sall2\"]", "do": null }, { "gene_id": 50527, "description": "endoplasmic reticulum oxidoreductase 1 alpha", "gene_symbol": "[\"Ero1a\"]", "do": null }, { "gene_id": 50528, "description": "transmembrane protease, serine 2", "gene_symbol": "[\"Tmprss2\"]", "do": null }, { "gene_id": 50530, "description": "microfibrillar associated protein 5", "gene_symbol": "[\"Mfap5\"]", "do": null }, { "gene_id": 50701, "description": "elastase, neutrophil expressed", "gene_symbol": "[\"Elane\"]", "do": null }, { "gene_id": 50702, "description": "complement factor H-related 1", "gene_symbol": "[\"Cfhr1\"]", "do": null }, { "gene_id": 50706, "description": "periostin, osteoblast specific factor", "gene_symbol": "[\"Postn\"]", "do": "[{\"label\":\"aggressive periodontitis\",\"id\":\"DOID:1474\"},{\"label\":\"bone structure disease\",\"id\":\"DOID:0080010\"}]" }, { "gene_id": 50720, "description": "sacsin", "gene_symbol": "[\"Sacs\"]", "do": "[{\"label\":\"Charlevoix-Saguenay spastic ataxia\",\"id\":\"DOID:0050946\"}]" }, { "gene_id": 50721, "description": "sirtuin 6", "gene_symbol": "[\"Sirt6\"]", "do": "[{\"label\":\"progeria\",\"id\":\"DOID:3911\"}]" }, { "gene_id": 50722, "description": "dickkopf-like 1", "gene_symbol": "[\"Dkkl1\"]", "do": null }, { "gene_id": 50723, "description": "icos ligand", "gene_symbol": "[\"Icosl\"]", "do": null }, { "gene_id": 50762, "description": "F-box protein 6", "gene_symbol": "[\"Fbxo6\"]", "do": null }, { "gene_id": 50765, "description": "transferrin receptor 2", "gene_symbol": "[\"Tfr2\"]", "do": "[{\"label\":\"hemochromatosis type 3\",\"id\":\"DOID:0111030\"}]" }, { "gene_id": 50766, "description": "cysteine rich transmembrane BMP regulator 1", "gene_symbol": "[\"Crim1\"]", "do": null }, { "gene_id": 50767, "description": "patatin-like phospholipase domain containing 6", "gene_symbol": "[\"Pnpla6\"]", "do": null }, { "gene_id": 50768, "description": "deleted in liver cancer 1", "gene_symbol": "[\"Dlc1\"]", "do": null }, { "gene_id": 50779, "description": "regulator of G-protein signaling 6", "gene_symbol": "[\"Rgs6\"]", "do": null }, { "gene_id": 50781, "description": "dickkopf WNT signaling pathway inhibitor 3", "gene_symbol": "[\"Dkk3\"]", "do": null }, { "gene_id": 50784, "description": "phospholipid phosphatase 2", "gene_symbol": "[\"Plpp2\"]", "do": null }, { "gene_id": 50785, "description": "heparan sulfate 6-O-sulfotransferase 1", "gene_symbol": "[\"Hs6st1\"]", "do": null }, { "gene_id": 50786, "description": "heparan sulfate 6-O-sulfotransferase 2", "gene_symbol": "[\"Hs6st2\"]", "do": null }, { "gene_id": 50787, "description": "heparan sulfate 6-O-sulfotransferase 3", "gene_symbol": "[\"Hs6st3\"]", "do": null }, { "gene_id": 50791, "description": "membrane associated guanylate kinase, WW and PDZ domain containing 2", "gene_symbol": "[\"Magi2\"]", "do": null }, { "gene_id": 50793, "description": "origin recognition complex, subunit 3", "gene_symbol": "[\"Orc3\"]", "do": null }, { "gene_id": 50796, "description": "doublesex and mab-3 related transcription factor 1", "gene_symbol": "[\"Dmrt1\"]", "do": null }, { "gene_id": 50798, "description": "glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase", "gene_symbol": "[\"Gne\"]", "do": null }, { "gene_id": 50799, "description": "solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13", "gene_symbol": "[\"Slc25a13\"]", "do": null }, { "gene_id": 50876, "description": "tropomodulin 2", "gene_symbol": "[\"Tmod2\"]", "do": null }, { "gene_id": 50877, "description": "neuraminidase 3", "gene_symbol": "[\"Neu3\"]", "do": null }, { "gene_id": 50884, "description": "NCK-associated protein 1", "gene_symbol": "[\"Nckap1\"]", "do": null }, { "gene_id": 50905, "description": "interleukin 17 receptor B", "gene_symbol": "[\"Il17rb\"]", "do": null }, { "gene_id": 50908, "description": "complement component 1, s subcomponent 1", "gene_symbol": "[\"C1s1\"]", "do": null }, { "gene_id": 50909, "description": "complement component 1, r subcomponent A", "gene_symbol": "[\"C1ra\"]", "do": null }, { "gene_id": 50917, "description": "galactosamine (N-acetyl)-6-sulfatase", "gene_symbol": "[\"Galns\"]", "do": "[{\"label\":\"mucopolysaccharidosis IV\",\"id\":\"DOID:12804\"}]" }, { "gene_id": 50927, "description": "nuclear autoantigenic sperm protein (histone-binding)", "gene_symbol": "[\"Nasp\"]", "do": null }, { "gene_id": 50928, "description": "killer cell lectin-like receptor subfamily G, member 1", "gene_symbol": "[\"Klrg1\"]", "do": null }, { "gene_id": 50929, "description": "interleukin 22", "gene_symbol": "[\"Il22\"]", "do": "[{\"label\":\"liposarcoma\",\"id\":\"DOID:3382\"}]" }, { "gene_id": 50930, "description": "tumor necrosis factor (ligand) superfamily, member 14", "gene_symbol": "[\"Tnfsf14\"]", "do": "[{\"label\":\"IgA glomerulonephritis\",\"id\":\"DOID:2986\"}]" }, { "gene_id": 50931, "description": "interleukin 27 receptor, alpha", "gene_symbol": "[\"Il27ra\"]", "do": null }, { "gene_id": 50932, "description": "misshapen-like kinase 1 (zebrafish)", "gene_symbol": "[\"Mink1\"]", "do": null }, { "gene_id": 50935, "description": "ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6", "gene_symbol": "[\"St6galnac6\"]", "do": null }, { "gene_id": 50997, "description": "membrane protein, palmitoylated 2 (MAGUK p55 subfamily member 2)", "gene_symbol": "[\"Mpp2\"]", "do": null }, { "gene_id": 51789, "description": "tyrosine kinase, non-receptor, 2", "gene_symbol": "[\"Tnk2\"]", "do": null }, { "gene_id": 51793, "description": "DDAH family member 2, ADMA independent", "gene_symbol": "[\"Ddah2\"]", "do": null }, { "gene_id": 51795, "description": "sushi-repeat-containing protein", "gene_symbol": "[\"Srpx\"]", "do": null }, { "gene_id": 51796, "description": "serine/arginine repetitive matrix 1", "gene_symbol": "[\"Srrm1\"]", "do": null }, { "gene_id": 51810, "description": "heterogeneous nuclear ribonucleoprotein U", "gene_symbol": "[\"Hnrnpu\"]", "do": "[{\"label\":\"developmental and epileptic encephalopathy 54\",\"id\":\"DOID:0080418\"}]" }, { "gene_id": 51811, "description": "C-type lectin domain family 4, member f", "gene_symbol": "[\"Clec4f\"]", "do": null }, { "gene_id": 51812, "description": "microspherule protein 1", "gene_symbol": "[\"Mcrs1\"]", "do": null }, { "gene_id": 51886, "description": "far upstream element (FUSE) binding protein 1", "gene_symbol": "[\"Fubp1\"]", "do": null }, { "gene_id": 52009, "description": "Jupiter microtubule associated homolog 2", "gene_symbol": "[\"Jpt2\"]", "do": null }, { "gene_id": 52014, "description": "NUS1 dehydrodolichyl diphosphate synthase subunit", "gene_symbol": "[\"Nus1\"]", "do": null }, { "gene_id": 52020, "description": "uromodulin-like 1", "gene_symbol": "[\"Umodl1\"]", "do": null }, { "gene_id": 52055, "description": "RAB11 family interacting protein 5 (class I)", "gene_symbol": "[\"Rab11fip5\"]", "do": null }, { "gene_id": 52118, "description": "poliovirus receptor", "gene_symbol": "[\"Pvr\"]", "do": null }, { "gene_id": 52120, "description": "heparan-alpha-glucosaminide N-acetyltransferase", "gene_symbol": "[\"Hgsnat\"]", "do": "[{\"label\":\"mucopolysaccharidosis III\",\"id\":\"DOID:12801\"}]" }, { "gene_id": 52150, "description": "potassium inwardly-rectifying channel, subfamily K, member 6", "gene_symbol": "[\"Kcnk6\"]", "do": null }, { "gene_id": 52187, "description": "Ras-related GTP binding D", "gene_symbol": "[\"Rragd\"]", "do": null }, { "gene_id": 52331, "description": "starch binding domain 1", "gene_symbol": "[\"Stbd1\"]", "do": null }, { "gene_id": 52335, "description": "ataxin 1-like", "gene_symbol": "[\"Atxn1l\"]", "do": null }, { "gene_id": 52348, "description": "vacuolar protein sorting 37A", "gene_symbol": "[\"Vps37a\"]", "do": null }, { "gene_id": 52357, "description": "WW, C2 and coiled-coil domain containing 2", "gene_symbol": "[\"Wwc2\"]", "do": null }, { "gene_id": 52377, "description": "reticulocalbin 3, EF-hand calcium binding domain", "gene_symbol": "[\"Rcn3\"]", "do": null }, { "gene_id": 52397, "description": "zinc finger protein 644", "gene_symbol": "[\"Zfp644\"]", "do": null }, { "gene_id": 52463, "description": "tet methylcytosine dioxygenase 1", "gene_symbol": "[\"Tet1\"]", "do": null }, { "gene_id": 52466, "description": "solute carrier family 46, member 1", "gene_symbol": "[\"Slc46a1\"]", "do": null }, { "gene_id": 52538, "description": "acetyl-CoA acyltransferase 2", "gene_symbol": "[\"Acaa2\"]", "do": null }, { "gene_id": 52551, "description": "small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha", "gene_symbol": "[\"Sgta\"]", "do": null }, { "gene_id": 52552, "description": "poly (ADP-ribose) polymerase family, member 8", "gene_symbol": "[\"Parp8\"]", "do": null }, { "gene_id": 52588, "description": "tetraspanin 14", "gene_symbol": "[\"Tspan14\"]", "do": null }, { "gene_id": 52614, "description": "adhesion G protein-coupled receptor E4", "gene_symbol": "[\"Adgre4\"]", "do": null }, { "gene_id": 52635, "description": "extended synaptotagmin-like protein 2", "gene_symbol": "[\"Esyt2\"]", "do": null }, { "gene_id": 52637, "description": "CDGSH iron sulfur domain 1", "gene_symbol": "[\"Cisd1\"]", "do": null }, { "gene_id": 52639, "description": "WD repeat domain, phosphoinositide interacting 1", "gene_symbol": "[\"Wipi1\"]", "do": null }, { "gene_id": 52653, "description": "NudC domain containing 2", "gene_symbol": "[\"Nudcd2\"]", "do": null }, { "gene_id": 52666, "description": "Rho guanine nucleotide exchange factor 25", "gene_symbol": "[\"Arhgef25\"]", "do": null }, { "gene_id": 52685, "description": "CD300 molecule like family member G", "gene_symbol": "[\"Cd300lg\"]", "do": null }, { "gene_id": 52696, "description": "ZW10 interactor", "gene_symbol": "[\"Zwint\"]", "do": null }, { "gene_id": 52710, "description": "solute carrier protein 52, member 2", "gene_symbol": "[\"Slc52a2\"]", "do": null }, { "gene_id": 52712, "description": "zinc finger with KRAB and SCAN domains 6", "gene_symbol": "[\"Zkscan6\"]", "do": null }, { "gene_id": 52717, "description": "anaphase promoting complex subunit 16", "gene_symbol": "[\"Anapc16\"]", "do": null }, { "gene_id": 52793, "description": "FAM3 metabolism regulating signaling molecule B", "gene_symbol": "[\"Fam3b\"]", "do": null }, { "gene_id": 52837, "description": "thioredoxin-related transmembrane protein 4", "gene_symbol": "[\"Tmx4\"]", "do": null }, { "gene_id": 52855, "description": "leukocyte-associated Ig-like receptor 1", "gene_symbol": "[\"Lair1\"]", "do": null }, { "gene_id": 52897, "description": "RNA binding protein, fox-1 homolog (C. elegans) 3", "gene_symbol": "[\"Rbfox3\"]", "do": null }, { "gene_id": 53311, "description": "myosin binding protein H", "gene_symbol": "[\"Mybph\"]", "do": null }, { "gene_id": 53312, "description": "negative regulator of ubiquitin-like proteins 1", "gene_symbol": "[\"Nub1\"]", "do": null }, { "gene_id": 53313, "description": "ATPase, Ca++ transporting, ubiquitous", "gene_symbol": "[\"Atp2a3\"]", "do": null }, { "gene_id": 53317, "description": "pleiotropic regulator 1", "gene_symbol": "[\"Plrg1\"]", "do": null }, { "gene_id": 53319, "description": "nuclear RNA export factor 1", "gene_symbol": "[\"Nxf1\"]", "do": null }, { "gene_id": 53320, "description": "folate hydrolase 1", "gene_symbol": "[\"Folh1\"]", "do": null }, { "gene_id": 53321, "description": "contactin associated protein-like 1", "gene_symbol": "[\"Cntnap1\"]", "do": null }, { "gene_id": 53322, "description": "nucleobindin 2", "gene_symbol": "[\"Nucb2\"]", "do": null }, { "gene_id": 53324, "description": "neuronal pentraxin 2", "gene_symbol": "[\"Nptx2\"]", "do": null }, { "gene_id": 53332, "description": "myotubularin related protein 1", "gene_symbol": "[\"Mtmr1\"]", "do": null }, { "gene_id": 53333, "description": "translocase of outer mitochondrial membrane 40", "gene_symbol": "[\"Tomm40\"]", "do": null }, { "gene_id": 53356, "description": "eukaryotic translation initiation factor 3, subunit G", "gene_symbol": "[\"Eif3g\"]", "do": null }, { "gene_id": 53357, "description": "phospholipase A2, group VI", "gene_symbol": "[\"Pla2g6\"]", "do": "[{\"label\":\"Parkinson's disease 14\",\"id\":\"DOID:0060900\"},{\"label\":\"neurodegeneration with brain iron accumulation 2a\",\"id\":\"DOID:0110735\"}]" }, { "gene_id": 53374, "description": "carbohydrate sulfotransferase 3", "gene_symbol": "[\"Chst3\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 53375, "description": "metaxin 2", "gene_symbol": "[\"Mtx2\"]", "do": null }, { "gene_id": 53412, "description": "protein phosphatase 1, regulatory subunit 3C", "gene_symbol": "[\"Ppp1r3c\"]", "do": "[{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 53418, "description": "UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2", "gene_symbol": "[\"B4galt2\"]", "do": null }, { "gene_id": 53419, "description": "corin, serine peptidase", "gene_symbol": "[\"Corin\"]", "do": null }, { "gene_id": 53599, "description": "CD164 antigen", "gene_symbol": "[\"Cd164\"]", "do": null }, { "gene_id": 53601, "description": "protocadherin 12", "gene_symbol": "[\"Pcdh12\"]", "do": null }, { "gene_id": 53603, "description": "thymic stromal lymphopoietin", "gene_symbol": "[\"Tslp\"]", "do": "[{\"label\":\"atopic dermatitis\",\"id\":\"DOID:3310\"},{\"label\":\"autoimmune hemolytic anemia\",\"id\":\"DOID:718\"},{\"label\":\"cryoglobulinemia\",\"id\":\"DOID:2917\"},{\"label\":\"membranoproliferative glomerulonephritis\",\"id\":\"DOID:2920\"}]" }, { "gene_id": 53604, "description": "zona pellucida binding protein", "gene_symbol": "[\"Zpbp\"]", "do": null }, { "gene_id": 53609, "description": "CLK4-associating serine/arginine rich protein", "gene_symbol": "[\"Clasrp\"]", "do": null }, { "gene_id": 53610, "description": "non-POU-domain-containing, octamer binding protein", "gene_symbol": "[\"Nono\"]", "do": null }, { "gene_id": 53614, "description": "reversion-inducing-cysteine-rich protein with kazal motifs", "gene_symbol": "[\"Reck\"]", "do": null }, { "gene_id": 53618, "description": "fucosyltransferase 8", "gene_symbol": "[\"Fut8\"]", "do": "[{\"label\":\"pulmonary emphysema\",\"id\":\"DOID:9675\"}]" }, { "gene_id": 53621, "description": "CCR4-NOT transcription complex, subunit 4", "gene_symbol": "[\"Cnot4\"]", "do": null }, { "gene_id": 53623, "description": "glutamate receptor, ionotropic, AMPA3 (alpha 3)", "gene_symbol": "[\"Gria3\"]", "do": null }, { "gene_id": 53625, "description": "UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2", "gene_symbol": "[\"B3gnt2\"]", "do": null }, { "gene_id": 53761, "description": "proline-rich coiled-coil 2A", "gene_symbol": "[\"Prrc2a\"]", "do": null }, { "gene_id": 53791, "description": "toll-like receptor 5", "gene_symbol": "[\"Tlr5\"]", "do": null }, { "gene_id": 53857, "description": "tubulin, alpha 8", "gene_symbol": "[\"Tuba8\"]", "do": null }, { "gene_id": 53860, "description": "septin 9", "gene_symbol": "[\"Septin9\"]", "do": null }, { "gene_id": 53867, "description": "collagen, type V, alpha 3", "gene_symbol": "[\"Col5a3\"]", "do": null }, { "gene_id": 53870, "description": "contactin 6", "gene_symbol": "[\"Cntn6\"]", "do": null }, { "gene_id": 53871, "description": "polycystic kidney disease 2-like 2", "gene_symbol": "[\"Pkd2l2\"]", "do": null }, { "gene_id": 53872, "description": "cell cycle associated protein 1", "gene_symbol": "[\"Caprin1\"]", "do": null }, { "gene_id": 53876, "description": "eosinophil-associated, ribonuclease A family, member 3", "gene_symbol": "[\"Ear3\"]", "do": null }, { "gene_id": 53877, "description": "eosinophil-associated, ribonuclease A family, member 4", "gene_symbol": "[\"Ear4\"]", "do": null }, { "gene_id": 53881, "description": "solute carrier family 5 (inositol transporters), member 3", "gene_symbol": "[\"Slc5a3\"]", "do": null }, { "gene_id": 53883, "description": "cadherin, EGF LAG seven-pass G-type receptor 2", "gene_symbol": "[\"Celsr2\"]", "do": "[{\"label\":\"hydrocephalus\",\"id\":\"DOID:10908\"}]" }, { "gene_id": 53885, "description": "nephronophthisis 1 (juvenile) homolog (human)", "gene_symbol": "[\"Nphp1\"]", "do": null }, { "gene_id": 53893, "description": "nudix hydrolase 5", "gene_symbol": "[\"Nudt5\"]", "do": null }, { "gene_id": 53897, "description": "galactose-3-O-sulfotransferase 1", "gene_symbol": "[\"Gal3st1\"]", "do": null }, { "gene_id": 53945, "description": "solute carrier family 40 (iron-regulated transporter), member 1", "gene_symbol": "[\"Slc40a1\"]", "do": "[{\"label\":\"hemochromatosis type 4\",\"id\":\"DOID:0111028\"}]" }, { "gene_id": 53972, "description": "neuronal guanine nucleotide exchange factor", "gene_symbol": "[\"Ngef\"]", "do": null }, { "gene_id": 53975, "description": "DEAD box helicase 20", "gene_symbol": "[\"Ddx20\"]", "do": null }, { "gene_id": 53978, "description": "lysophosphatidic acid receptor 2", "gene_symbol": "[\"Lpar2\"]", "do": null }, { "gene_id": 54003, "description": "NEL-like 2", "gene_symbol": "[\"Nell2\"]", "do": null }, { "gene_id": 54006, "description": "DEAF1, transcription factor", "gene_symbol": "[\"Deaf1\"]", "do": null }, { "gene_id": 54126, "description": "Rho guanine nucleotide exchange factor", "gene_symbol": "[\"Arhgef7\"]", "do": null }, { "gene_id": 54128, "description": "phosphomannomutase 2", "gene_symbol": "[\"Pmm2\"]", "do": "[{\"label\":\"congenital disorder of glycosylation type I\",\"id\":\"DOID:0050570\"}]" }, { "gene_id": 54132, "description": "PDZ and LIM domain 1 (elfin)", "gene_symbol": "[\"Pdlim1\"]", "do": null }, { "gene_id": 54140, "description": "arginine vasopressin receptor 1A", "gene_symbol": "[\"Avpr1a\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 54141, "description": "sperm associated antigen 5", "gene_symbol": "[\"Spag5\"]", "do": null }, { "gene_id": 54156, "description": "EGF-like-domain, multiple 6", "gene_symbol": "[\"Egfl6\"]", "do": null }, { "gene_id": 54159, "description": "ribonuclease, RNase A family, 2B (liver, eosinophil-derived neurotoxin)", "gene_symbol": "[\"Rnase2b\"]", "do": null }, { "gene_id": 54160, "description": "coatomer protein complex, subunit gamma 2", "gene_symbol": "[\"Copg2\"]", "do": null }, { "gene_id": 54167, "description": "inducible T cell co-stimulator", "gene_symbol": "[\"Icos\"]", "do": "[{\"label\":\"common variable immunodeficiency\",\"id\":\"DOID:12177\"}]" }, { "gene_id": 54169, "description": "K(lysine) acetyltransferase 6B", "gene_symbol": "[\"Kat6b\"]", "do": "[{\"label\":\"Noonan syndrome\",\"id\":\"DOID:3490\"}]" }, { "gene_id": 54170, "description": "Ras-related GTP binding C", "gene_symbol": "[\"Rragc\"]", "do": null }, { "gene_id": 54199, "description": "C-C motif chemokine receptor-like 2", "gene_symbol": "[\"Ccrl2\"]", "do": null }, { "gene_id": 54215, "description": "CD160 antigen", "gene_symbol": "[\"Cd160\"]", "do": null }, { "gene_id": 54216, "description": "protocadherin 7", "gene_symbol": "[\"Pcdh7\"]", "do": null }, { "gene_id": 54218, "description": "UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 4", "gene_symbol": "[\"B3galt4\"]", "do": null }, { "gene_id": 54219, "description": "CD320 antigen", "gene_symbol": "[\"Cd320\"]", "do": "[{\"label\":\"methylmalonic acidemia due to transcobalamin receptor defect\",\"id\":\"DOID:0060741\"}]" }, { "gene_id": 54324, "description": "Rho guanine nucleotide exchange factor 5", "gene_symbol": "[\"Arhgef5\"]", "do": null }, { "gene_id": 54338, "description": "solute carrier family 23 (nucleobase transporters), member 2", "gene_symbol": "[\"Slc23a2\"]", "do": null }, { "gene_id": 54343, "description": "activating transcription factor 7 interacting protein", "gene_symbol": "[\"Atf7ip\"]", "do": null }, { "gene_id": 54367, "description": "zinc finger protein 326", "gene_symbol": "[\"Zfp326\"]", "do": null }, { "gene_id": 54368, "description": "glycoprotein 9 platelet", "gene_symbol": "[\"Gp9\"]", "do": null }, { "gene_id": 54371, "description": "carbohydrate sulfotransferase 2", "gene_symbol": "[\"Chst2\"]", "do": null }, { "gene_id": 54373, "description": "serine protease 16 (thymus)", "gene_symbol": "[\"Prss16\"]", "do": null }, { "gene_id": 54376, "description": "calcium channel, voltage-dependent, gamma subunit 3", "gene_symbol": "[\"Cacng3\"]", "do": null }, { "gene_id": 54377, "description": "calcium channel, voltage-dependent, gamma subunit 4", "gene_symbol": "[\"Cacng4\"]", "do": null }, { "gene_id": 54378, "description": "calcium channel, voltage-dependent, gamma subunit 6", "gene_symbol": "[\"Cacng6\"]", "do": null }, { "gene_id": 54381, "description": "carboxypeptidase Q", "gene_symbol": "[\"Cpq\"]", "do": null }, { "gene_id": 54383, "description": "polyhomeotic 2", "gene_symbol": "[\"Phc2\"]", "do": null }, { "gene_id": 54387, "description": "minichromosome maintenance complex component 3 associated protein", "gene_symbol": "[\"Mcm3ap\"]", "do": null }, { "gene_id": 54390, "description": "suppression inducing transmembrane adaptor 1", "gene_symbol": "[\"Sit1\"]", "do": null }, { "gene_id": 54393, "description": "gamma-aminobutyric acid type B receptor subunit 1", "gene_symbol": "[\"Gabbr1\"]", "do": null }, { "gene_id": 54397, "description": "palmitoyl-protein thioesterase 2", "gene_symbol": "[\"Ppt2\"]", "do": "[{\"label\":\"neuronal ceroid lipofuscinosis\",\"id\":\"DOID:14503\"}]" }, { "gene_id": 54403, "description": "solute carrier family 4 (anion exchanger), member 4", "gene_symbol": "[\"Slc4a4\"]", "do": "[{\"label\":\"renal tubular acidosis\",\"id\":\"DOID:14219\"}]" }, { "gene_id": 54409, "description": "receptor (calcitonin) activity modifying protein 2", "gene_symbol": "[\"Ramp2\"]", "do": null }, { "gene_id": 54411, "description": "ATPase, H+ transporting, lysosomal accessory protein 1", "gene_symbol": "[\"Atp6ap1\"]", "do": null }, { "gene_id": 54418, "description": "formin 2", "gene_symbol": "[\"Fmn2\"]", "do": null }, { "gene_id": 54426, "description": "hepatocyte growth factor activator", "gene_symbol": "[\"Hgfac\"]", "do": null }, { "gene_id": 54445, "description": "unc-93 homolog B1, TLR signaling regulator", "gene_symbol": "[\"Unc93b1\"]", "do": null }, { "gene_id": 54446, "description": "nuclear factor of activated T cells 5", "gene_symbol": "[\"Nfat5\"]", "do": null }, { "gene_id": 54447, "description": "N-acylsphingosine amidohydrolase 2", "gene_symbol": "[\"Asah2\"]", "do": null }, { "gene_id": 54485, "description": "delta like canonical Notch ligand 4", "gene_symbol": "[\"Dll4\"]", "do": "[{\"label\":\"Adams-Oliver syndrome\",\"id\":\"DOID:0060227\"}]" }, { "gene_id": 54563, "description": "nucleoporin 210", "gene_symbol": "[\"Nup210\"]", "do": null }, { "gene_id": 54598, "description": "calcitonin receptor-like", "gene_symbol": "[\"Calcrl\"]", "do": null }, { "gene_id": 54604, "description": "pecanex 1", "gene_symbol": "[\"Pcnx1\"]", "do": null }, { "gene_id": 54608, "description": "abhydrolase domain containing 2", "gene_symbol": "[\"Abhd2\"]", "do": null }, { "gene_id": 54609, "description": "ubiquilin 2", "gene_symbol": "[\"Ubqln2\"]", "do": null }, { "gene_id": 54613, "description": "ST3 beta-galactoside alpha-2,3-sialyltransferase 6", "gene_symbol": "[\"St3gal6\"]", "do": null }, { "gene_id": 54616, "description": "exostosin-like glycosyltransferase 3", "gene_symbol": "[\"Extl3\"]", "do": null }, { "gene_id": 54624, "description": "Paf1, RNA polymerase II complex component", "gene_symbol": "[\"Paf1\"]", "do": null }, { "gene_id": 54631, "description": "nephrosis 1, nephrin", "gene_symbol": "[\"Nphs1\"]", "do": "[{\"label\":\"nephrotic syndrome\",\"id\":\"DOID:1184\"}]" }, { "gene_id": 54635, "description": "platelet-derived growth factor, C polypeptide", "gene_symbol": "[\"Pdgfc\"]", "do": null }, { "gene_id": 54636, "description": "WD repeat domain 45", "gene_symbol": "[\"Wdr45\"]", "do": null }, { "gene_id": 54645, "description": "GRIP1 associated protein 1", "gene_symbol": "[\"Gripap1\"]", "do": null }, { "gene_id": 54646, "description": "protein phosphatase 1, regulatory subunit 3F", "gene_symbol": "[\"Ppp1r3f\"]", "do": null }, { "gene_id": 54652, "description": "calcium channel, voltage-dependent, alpha 1F subunit", "gene_symbol": "[\"Cacna1f\"]", "do": "[{\"label\":\"congenital stationary night blindness 2A\",\"id\":\"DOID:0110871\"}]" }, { "gene_id": 54672, "description": "adhesion G protein-coupled receptor G3", "gene_symbol": "[\"Adgrg3\"]", "do": null }, { "gene_id": 54698, "description": "cytotoxic and regulatory T cell molecule", "gene_symbol": "[\"Crtam\"]", "do": null }, { "gene_id": 54710, "description": "heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1", "gene_symbol": "[\"Hs3st3b1\"]", "do": null }, { "gene_id": 54712, "description": "plexin C1", "gene_symbol": "[\"Plxnc1\"]", "do": null }, { "gene_id": 54725, "description": "cell adhesion molecule 1", "gene_symbol": "[\"Cadm1\"]", "do": null }, { "gene_id": 55935, "description": "formin binding protein 4", "gene_symbol": "[\"Fnbp4\"]", "do": null }, { "gene_id": 55961, "description": "solute carrier family 13 (sodium/sulfate symporters), member 1", "gene_symbol": "[\"Slc13a1\"]", "do": null }, { "gene_id": 55963, "description": "solute carrier family 1 (glutamate/neutral amino acid transporter), member 4", "gene_symbol": "[\"Slc1a4\"]", "do": "[{\"label\":\"spastic tetraplegia, thin corpus callosum, and progressive microcephaly\",\"id\":\"DOID:0070537\"}]" }, { "gene_id": 55979, "description": "1-acylglycerol-3-phosphate O-acyltransferase 1", "gene_symbol": "[\"Agpat1\"]", "do": null }, { "gene_id": 55981, "description": "phosphatidylinositol glycan anchor biosynthesis, class B", "gene_symbol": "[\"Pigb\"]", "do": null }, { "gene_id": 55987, "description": "carboxypeptidase X, M14 family member 2", "gene_symbol": "[\"Cpxm2\"]", "do": null }, { "gene_id": 55991, "description": "pannexin 1", "gene_symbol": "[\"Panx1\"]", "do": null }, { "gene_id": 56012, "description": "phosphoglycerate mutase 2", "gene_symbol": "[\"Pgam2\"]", "do": null }, { "gene_id": 56013, "description": "SRC kinase signaling inhibitor 1", "gene_symbol": "[\"Srcin1\"]", "do": null }, { "gene_id": 56017, "description": "solute carrier family 2, (facilitated glucose transporter), member 8", "gene_symbol": "[\"Slc2a8\"]", "do": null }, { "gene_id": 56030, "description": "transmembrane protein 131", "gene_symbol": "[\"Tmem131\"]", "do": null }, { "gene_id": 56031, "description": "peptidylprolyl isomerase E (cyclophilin E)", "gene_symbol": "[\"Ppie\"]", "do": null }, { "gene_id": 56044, "description": "Ras like proto-oncogene A", "gene_symbol": "[\"Rala\"]", "do": null }, { "gene_id": 56047, "description": "mesothelin", "gene_symbol": "[\"Msln\"]", "do": null }, { "gene_id": 56069, "description": "interleukin 17B", "gene_symbol": "[\"Il17b\"]", "do": null }, { "gene_id": 56070, "description": "transcription elongation regulator 1 (CA150)", "gene_symbol": "[\"Tcerg1\"]", "do": null }, { "gene_id": 56079, "description": "astrotactin 2", "gene_symbol": "[\"Astn2\"]", "do": null }, { "gene_id": 56089, "description": "receptor (calcitonin) activity modifying protein 3", "gene_symbol": "[\"Ramp3\"]", "do": null }, { "gene_id": 56092, "description": "cathepsin 7", "gene_symbol": "[\"Cts7\"]", "do": null }, { "gene_id": 56094, "description": "cathepsin 8", "gene_symbol": "[\"Cts8\"]", "do": null }, { "gene_id": 56174, "description": "N-acetylglucosamine kinase", "gene_symbol": "[\"Nagk\"]", "do": null }, { "gene_id": 56175, "description": "beta-site APP-cleaving enzyme 2", "gene_symbol": "[\"Bace2\"]", "do": null }, { "gene_id": 56176, "description": "phosphatidylinositol glycan anchor biosynthesis, class P", "gene_symbol": "[\"Pigp\"]", "do": null }, { "gene_id": 56177, "description": "olfactomedin 1", "gene_symbol": "[\"Olfm1\"]", "do": null }, { "gene_id": 56195, "description": "polypyrimidine tract binding protein 2", "gene_symbol": "[\"Ptbp2\"]", "do": null }, { "gene_id": 56209, "description": "glycerophosphodiester phosphodiesterase 1", "gene_symbol": "[\"Gde1\"]", "do": null }, { "gene_id": 56215, "description": "apoptotic chromatin condensation inducer 1", "gene_symbol": "[\"Acin1\"]", "do": null }, { "gene_id": 56216, "description": "syntaxin 1B", "gene_symbol": "[\"Stx1b\"]", "do": null }, { "gene_id": 56217, "description": "protein associated with LIN7 1, MAGUK family member", "gene_symbol": "[\"Pals1\"]", "do": "[{\"label\":\"Leber congenital amaurosis\",\"id\":\"DOID:14791\"}]" }, { "gene_id": 56219, "description": "exostosin-like glycosyltransferase 1", "gene_symbol": "[\"Extl1\"]", "do": null }, { "gene_id": 56221, "description": "C-C motif chemokine ligand 24", "gene_symbol": "[\"Ccl24\"]", "do": null }, { "gene_id": 56224, "description": "tetraspanin 5", "gene_symbol": "[\"Tspan5\"]", "do": null }, { "gene_id": 56229, "description": "thrombospondin, type I, domain 1", "gene_symbol": "[\"Thsd1\"]", "do": null }, { "gene_id": 56258, "description": "heterogeneous nuclear ribonucleoprotein H2", "gene_symbol": "[\"Hnrnph2\"]", "do": "[{\"label\":\"syndromic X-linked intellectual developmental disorder bain type\",\"id\":\"DOID:0070538\"}]" }, { "gene_id": 56264, "description": "carboxypeptidase X, M14 family member 1", "gene_symbol": "[\"Cpxm1\"]", "do": null }, { "gene_id": 56275, "description": "RNA binding motif protein 14", "gene_symbol": "[\"Rbm14\"]", "do": null }, { "gene_id": 56282, "description": "mitochondrial ribosomal protein L12", "gene_symbol": "[\"Mrpl12\"]", "do": null }, { "gene_id": 56289, "description": "Ras association (RalGDS/AF-6) domain family member 1", "gene_symbol": "[\"Rassf1\"]", "do": null }, { "gene_id": 56297, "description": "ADP-ribosylation factor-like 6", "gene_symbol": "[\"Arl6\"]", "do": "[{\"label\":\"Bardet-Biedl syndrome 3\",\"id\":\"DOID:0110125\"}]" }, { "gene_id": 56307, "description": "methionine aminopeptidase 2", "gene_symbol": "[\"Metap2\"]", "do": null }, { "gene_id": 56310, "description": "G protein pathway suppressor 2", "gene_symbol": "[\"Gps2\"]", "do": null }, { "gene_id": 56315, "description": "Rhesus blood group-associated C glycoprotein", "gene_symbol": "[\"Rhcg\"]", "do": null }, { "gene_id": 56316, "description": "gamma-glutamyl carboxylase", "gene_symbol": "[\"Ggcx\"]", "do": null }, { "gene_id": 56317, "description": "anaphase promoting complex subunit 7", "gene_symbol": "[\"Anapc7\"]", "do": "[{\"label\":\"syndromic intellectual disability\",\"id\":\"DOID:0050888\"}]" }, { "gene_id": 56318, "description": "acid phosphatase 3", "gene_symbol": "[\"Acp3\"]", "do": "[{\"label\":\"prostate cancer\",\"id\":\"DOID:10283\"}]" }, { "gene_id": 56320, "description": "drebrin 1", "gene_symbol": "[\"Dbn1\"]", "do": null }, { "gene_id": 56324, "description": "signal transducing adaptor molecule (SH3 domain and ITAM motif) 2", "gene_symbol": "[\"Stam2\"]", "do": null }, { "gene_id": 56336, "description": "UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5", "gene_symbol": "[\"B4galt5\"]", "do": null }, { "gene_id": 56350, "description": "ADP-ribosylation factor-like 3", "gene_symbol": "[\"Arl3\"]", "do": "[{\"label\":\"autosomal recessive polycystic kidney disease\",\"id\":\"DOID:0110861\"},{\"label\":\"retinitis pigmentosa 2\",\"id\":\"DOID:0110415\"}]" }, { "gene_id": 56351, "description": "prostaglandin E synthase 3", "gene_symbol": "[\"Ptges3\"]", "do": null }, { "gene_id": 56354, "description": "DnaJ heat shock protein family (Hsp40) member C7", "gene_symbol": "[\"Dnajc7\"]", "do": null }, { "gene_id": 56356, "description": "glycolipid transfer protein", "gene_symbol": "[\"Gltp\"]", "do": null }, { "gene_id": 56363, "description": "transmembrane protein with EGF-like and two follistatin-like domains 2", "gene_symbol": "[\"Tmeff2\"]", "do": null }, { "gene_id": 56365, "description": "chloride channel, voltage-sensitive Kb", "gene_symbol": "[\"Clcnkb\"]", "do": "[{\"label\":\"Bartter disease type 3\",\"id\":\"DOID:0110144\"},{\"label\":\"Bartter disease\",\"id\":\"DOID:445\"}]" }, { "gene_id": 56370, "description": "transgelin 3", "gene_symbol": "[\"Tagln3\"]", "do": null }, { "gene_id": 56373, "description": "carboxypeptidase B2", "gene_symbol": "[\"Cpb2\"]", "do": null }, { "gene_id": 56374, "description": "transmembrane protein 59", "gene_symbol": "[\"Tmem59\"]", "do": null }, { "gene_id": 56375, "description": "UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 4", "gene_symbol": "[\"B4galt4\"]", "do": null }, { "gene_id": 56376, "description": "PDZ and LIM domain 5", "gene_symbol": "[\"Pdlim5\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 56379, "description": "potassium inwardly-rectifying channel, subfamily J, member 1", "gene_symbol": "[\"Kcnj1\"]", "do": "[{\"label\":\"Bartter disease type 2\",\"id\":\"DOID:0110143\"}]" }, { "gene_id": 56380, "description": "AT-rich interaction domain 3B", "gene_symbol": "[\"Arid3b\"]", "do": null }, { "gene_id": 56381, "description": "spen family transcription repressor", "gene_symbol": "[\"Spen\"]", "do": null }, { "gene_id": 56386, "description": "UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 6", "gene_symbol": "[\"B4galt6\"]", "do": null }, { "gene_id": 56389, "description": "syntaxin 5A", "gene_symbol": "[\"Stx5a\"]", "do": null }, { "gene_id": 56399, "description": "A kinase anchor protein 8", "gene_symbol": "[\"Akap8\"]", "do": null }, { "gene_id": 56401, "description": "prolyl 3-hydroxylase 1", "gene_symbol": "[\"P3h1\"]", "do": "[{\"label\":\"osteogenesis imperfecta type 8\",\"id\":\"DOID:0110336\"}]" }, { "gene_id": 56409, "description": "nudix hydrolase 3", "gene_symbol": "[\"Nudt3\"]", "do": null }, { "gene_id": 56410, "description": "cerebellin 3 precursor protein", "gene_symbol": "[\"Cbln3\"]", "do": null }, { "gene_id": 56417, "description": "adenosine deaminase, RNA-specific", "gene_symbol": "[\"Adar\"]", "do": "[{\"label\":\"Aicardi-Goutieres syndrome\",\"id\":\"DOID:0050629\"}]" }, { "gene_id": 56421, "description": "phosphofructokinase, platelet", "gene_symbol": "[\"Pfkp\"]", "do": null }, { "gene_id": 56422, "description": "Hbs1-like (S. cerevisiae)", "gene_symbol": "[\"Hbs1l\"]", "do": null }, { "gene_id": 56430, "description": "CAP-GLY domain containing linker protein 1", "gene_symbol": "[\"Clip1\"]", "do": null }, { "gene_id": 56431, "description": "destrin", "gene_symbol": "[\"Dstn\"]", "do": null }, { "gene_id": 56434, "description": "tetraspanin 3", "gene_symbol": "[\"Tspan3\"]", "do": null }, { "gene_id": 56436, "description": "adhesion regulating molecule 1 26S proteasome ubiquitin receptor", "gene_symbol": "[\"Adrm1\"]", "do": null }, { "gene_id": 56440, "description": "sorting nexin 1", "gene_symbol": "[\"Snx1\"]", "do": null }, { "gene_id": 56443, "description": "actin related protein 2/3 complex, subunit 1A", "gene_symbol": "[\"Arpc1a\"]", "do": null }, { "gene_id": 56444, "description": "ARP10 actin-related protein 10", "gene_symbol": "[\"Actr10\"]", "do": null }, { "gene_id": 56445, "description": "DnaJ heat shock protein family (Hsp40) member A2", "gene_symbol": "[\"Dnaja2\"]", "do": null }, { "gene_id": 56453, "description": "membrane-bound transcription factor peptidase, site 1", "gene_symbol": "[\"Mbtps1\"]", "do": "[{\"label\":\"idiopathic scoliosis\",\"id\":\"DOID:0060250\"}]" }, { "gene_id": 56454, "description": "aldehyde dehydrogenase 18 family, member A1", "gene_symbol": "[\"Aldh18a1\"]", "do": null }, { "gene_id": 56457, "description": "cleft lip and palate associated transmembrane protein 1", "gene_symbol": "[\"Clptm1\"]", "do": null }, { "gene_id": 56458, "description": "forkhead box O1", "gene_symbol": "[\"Foxo1\"]", "do": null }, { "gene_id": 56463, "description": "staphylococcal nuclease and tudor domain containing 1", "gene_symbol": "[\"Snd1\"]", "do": null }, { "gene_id": 56464, "description": "cathepsin F", "gene_symbol": "[\"Ctsf\"]", "do": null }, { "gene_id": 56470, "description": "regulator of G-protein signaling 19", "gene_symbol": "[\"Rgs19\"]", "do": null }, { "gene_id": 56485, "description": "solute carrier family 2 (facilitated glucose transporter), member 5", "gene_symbol": "[\"Slc2a5\"]", "do": null }, { "gene_id": 56490, "description": "zinc finger and BTB domain containing 20", "gene_symbol": "[\"Zbtb20\"]", "do": null }, { "gene_id": 56495, "description": "guided entry of tail-anchored proteins factor 3, ATPase", "gene_symbol": "[\"Get3\"]", "do": null }, { "gene_id": 56496, "description": "tetraspanin 6", "gene_symbol": "[\"Tspan6\"]", "do": null }, { "gene_id": 56504, "description": "serine/arginine-rich protein specific kinase 3", "gene_symbol": "[\"Srpk3\"]", "do": null }, { "gene_id": 56505, "description": "RuvB-like AAA ATPase 1", "gene_symbol": "[\"Ruvbl1\"]", "do": null }, { "gene_id": 56508, "description": "Rap guanine nucleotide exchange factor (GEF) 4", "gene_symbol": "[\"Rapgef4\"]", "do": null }, { "gene_id": 56517, "description": "solute carrier family 22 (organic cation transporter), member 21", "gene_symbol": "[\"Slc22a21\"]", "do": null }, { "gene_id": 56527, "description": "microtubule associated serine/threonine kinase 1", "gene_symbol": "[\"Mast1\"]", "do": "[{\"label\":\"mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations\",\"id\":\"DOID:0111403\"}]" }, { "gene_id": 56532, "description": "receptor-interacting serine-threonine kinase 3", "gene_symbol": "[\"Ripk3\"]", "do": null }, { "gene_id": 56538, "description": "kallikrein related-peptidase 11", "gene_symbol": "[\"Klk11\"]", "do": null }, { "gene_id": 56544, "description": "vomeronasal 2, receptor 1", "gene_symbol": "[\"Vmn2r1\"]", "do": null }, { "gene_id": 56546, "description": "secretory blood group 1", "gene_symbol": "[\"Sec1\"]", "do": null }, { "gene_id": 56552, "description": "vomeronasal 2, receptor 26", "gene_symbol": "[\"Vmn2r26\"]", "do": null }, { "gene_id": 56554, "description": "retinoic acid early transcript delta", "gene_symbol": "[\"Raet1d\"]", "do": null }, { "gene_id": 56619, "description": "C-type lectin domain family 4, member e", "gene_symbol": "[\"Clec4e\"]", "do": null }, { "gene_id": 56620, "description": "C-type lectin domain family 4, member n", "gene_symbol": "[\"Clec4n\"]", "do": null }, { "gene_id": 56622, "description": "a disintegrin and metallopeptidase domain 21", "gene_symbol": "[\"Adam21\"]", "do": null }, { "gene_id": 56629, "description": "deoxyribonuclease II beta", "gene_symbol": "[\"Dnase2b\"]", "do": "[{\"label\":\"cataract\",\"id\":\"DOID:83\"}]" }, { "gene_id": 56637, "description": "glycogen synthase kinase 3 beta", "gene_symbol": "[\"Gsk3b\"]", "do": null }, { "gene_id": 56640, "description": "kallikrein related-peptidase 4 (prostase, enamel matrix, prostate)", "gene_symbol": "[\"Klk4\"]", "do": null }, { "gene_id": 56643, "description": "solute carrier family 15 (oligopeptide transporter), member 1", "gene_symbol": "[\"Slc15a1\"]", "do": null }, { "gene_id": 56690, "description": "malonyl-CoA decarboxylase", "gene_symbol": "[\"Mlycd\"]", "do": null }, { "gene_id": 56693, "description": "cartilage associated protein", "gene_symbol": "[\"Crtap\"]", "do": "[{\"label\":\"osteogenesis imperfecta type 7\",\"id\":\"DOID:0110337\"}]" }, { "gene_id": 56696, "description": "G protein-coupled receptor 132", "gene_symbol": "[\"Gpr132\"]", "do": "[{\"label\":\"autoimmune disease\",\"id\":\"DOID:417\"}]" }, { "gene_id": 56697, "description": "A kinase anchor protein 10", "gene_symbol": "[\"Akap10\"]", "do": null }, { "gene_id": 56700, "description": "glycosylated lysosomal membrane protein", "gene_symbol": "[\"Glmp\"]", "do": null }, { "gene_id": 56708, "description": "cardiotrophin-like cytokine factor 1", "gene_symbol": "[\"Clcf1\"]", "do": null }, { "gene_id": 56710, "description": "bone morphogenic protein/retinoic acid inducible neural specific 1", "gene_symbol": "[\"Brinp1\"]", "do": "[{\"label\":\"attention deficit hyperactivity disorder\",\"id\":\"DOID:1094\"},{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 56717, "description": "mechanistic target of rapamycin kinase", "gene_symbol": "[\"Mtor\"]", "do": null }, { "gene_id": 56727, "description": "myo-inositol oxygenase", "gene_symbol": "[\"Miox\"]", "do": null }, { "gene_id": 56737, "description": "ALG2 alpha-1,3/1,6-mannosyltransferase", "gene_symbol": "[\"Alg2\"]", "do": null }, { "gene_id": 56741, "description": "immunoglobulin superfamily, DCC subclass, member 4", "gene_symbol": "[\"Igdcc4\"]", "do": null }, { "gene_id": 56742, "description": "proline/serine-rich coiled-coil 1", "gene_symbol": "[\"Psrc1\"]", "do": null }, { "gene_id": 56744, "description": "platelet factor 4", "gene_symbol": "[\"Pf4\"]", "do": null }, { "gene_id": 56745, "description": "C1q and tumor necrosis factor related protein 1", "gene_symbol": "[\"C1qtnf1\"]", "do": null }, { "gene_id": 56746, "description": "testis expressed gene 101", "gene_symbol": "[\"Tex101\"]", "do": null }, { "gene_id": 56747, "description": "seizure related 6 homolog like", "gene_symbol": "[\"Sez6l\"]", "do": null }, { "gene_id": 56748, "description": "NFU1 iron-sulfur cluster scaffold", "gene_symbol": "[\"Nfu1\"]", "do": null }, { "gene_id": 56752, "description": "aldehyde dehydrogenase 9, subfamily A1", "gene_symbol": "[\"Aldh9a1\"]", "do": null }, { "gene_id": 56753, "description": "tumor-associated calcium signal transducer 2", "gene_symbol": "[\"Tacstd2\"]", "do": null }, { "gene_id": 56760, "description": "C-type lectin domain family 1, member b", "gene_symbol": "[\"Clec1b\"]", "do": null }, { "gene_id": 56773, "description": "carbohydrate sulfotransferase 5", "gene_symbol": "[\"Chst5\"]", "do": null }, { "gene_id": 56774, "description": "solute carrier family 6 (neurotransmitter transporter), member 14", "gene_symbol": "[\"Slc6a14\"]", "do": null }, { "gene_id": 56786, "description": "TMEM9 domain family, member B", "gene_symbol": "[\"Tmem9b\"]", "do": null }, { "gene_id": 56788, "description": "signal peptide, CUB domain, EGF-like 2", "gene_symbol": "[\"Scube2\"]", "do": null }, { "gene_id": 56807, "description": "secretory carrier membrane protein 5", "gene_symbol": "[\"Scamp5\"]", "do": "[{\"label\":\"epilepsy\",\"id\":\"DOID:1826\"}]" }, { "gene_id": 56808, "description": "calcium channel, voltage-dependent, alpha 2/delta subunit 2", "gene_symbol": "[\"Cacna2d2\"]", "do": "[{\"label\":\"epilepsy\",\"id\":\"DOID:1826\"}]" }, { "gene_id": 56811, "description": "dickkopf WNT signaling pathway inhibitor 2", "gene_symbol": "[\"Dkk2\"]", "do": null }, { "gene_id": 56835, "description": "cathepsin R", "gene_symbol": "[\"Ctsr\"]", "do": null }, { "gene_id": 56838, "description": "C-C motif chemokine ligand 28", "gene_symbol": "[\"Ccl28\"]", "do": null }, { "gene_id": 56839, "description": "leucine-rich repeat LGI family, member 1", "gene_symbol": "[\"Lgi1\"]", "do": "[{\"label\":\"familial temporal lobe epilepsy 1\",\"id\":\"DOID:0060748\"}]" }, { "gene_id": 56844, "description": "tumor-suppressing subchromosomal transferable fragment 4", "gene_symbol": "[\"Tssc4\"]", "do": null }, { "gene_id": 56857, "description": "solute carrier family 37 (glycerol-3-phosphate transporter), member 2", "gene_symbol": "[\"Slc37a2\"]", "do": null }, { "gene_id": 56861, "description": "olfactory receptor family 5 subfamily P member 57", "gene_symbol": "[\"Or5p57\"]", "do": null }, { "gene_id": 56868, "description": "pregnancy-specific beta-1-glycoprotein 23", "gene_symbol": "[\"Psg23\"]", "do": null }, { "gene_id": 57014, "description": "5-hydroxytryptamine (serotonin) receptor 3B", "gene_symbol": "[\"Htr3b\"]", "do": null }, { "gene_id": 57138, "description": "solute carrier family 12, member 5", "gene_symbol": "[\"Slc12a5\"]", "do": "[{\"label\":\"epilepsy\",\"id\":\"DOID:1826\"}]" }, { "gene_id": 57230, "description": "SAP30 binding protein", "gene_symbol": "[\"Sap30bp\"]", "do": null }, { "gene_id": 57246, "description": "T-box 20", "gene_symbol": "[\"Tbx20\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 57248, "description": "lymphocyte antigen 6 family member I", "gene_symbol": "[\"Ly6i\"]", "do": null }, { "gene_id": 57249, "description": "gamma-aminobutyric acid type A receptor subunit theta", "gene_symbol": "[\"Gabrq\"]", "do": null }, { "gene_id": 57252, "description": "taste receptor, type 2, member 105", "gene_symbol": "[\"Tas2r105\"]", "do": null }, { "gene_id": 57253, "description": "taste receptor, type 2, member 108", "gene_symbol": "[\"Tas2r108\"]", "do": null }, { "gene_id": 57254, "description": "taste receptor, type 2, member 119", "gene_symbol": "[\"Tas2r119\"]", "do": null }, { "gene_id": 57256, "description": "serine protease 21", "gene_symbol": "[\"Prss21\"]", "do": null }, { "gene_id": 57258, "description": "exportin 4", "gene_symbol": "[\"Xpo4\"]", "do": null }, { "gene_id": 57259, "description": "transducer of ERBB2, 2", "gene_symbol": "[\"Tob2\"]", "do": null }, { "gene_id": 57260, "description": "leukotriene B4 receptor 2", "gene_symbol": "[\"Ltb4r2\"]", "do": null }, { "gene_id": 57265, "description": "frizzled class receptor 2", "gene_symbol": "[\"Fzd2\"]", "do": null }, { "gene_id": 57271, "description": "olfactory receptor family 4 subfamily E member 2", "gene_symbol": "[\"Or4e2\"]", "do": null }, { "gene_id": 57272, "description": "olfactory receptor family 4 subfamily C member 3D", "gene_symbol": "[\"Or4c3d\"]", "do": null }, { "gene_id": 57276, "description": "V-set and immunoglobulin domain containing 2", "gene_symbol": "[\"Vsig2\"]", "do": null }, { "gene_id": 57278, "description": "basal cell adhesion molecule", "gene_symbol": "[\"Bcam\"]", "do": null }, { "gene_id": 57296, "description": "proteasome (prosome, macropain) 26S subunit, non-ATPase, 8", "gene_symbol": "[\"Psmd8\"]", "do": null }, { "gene_id": 57319, "description": "sphingomyelin phosphodiesterase, acid-like 3A", "gene_symbol": "[\"Smpdl3a\"]", "do": null }, { "gene_id": 57320, "description": "Parkinson disease (autosomal recessive, early onset) 7", "gene_symbol": "[\"Park7\"]", "do": "[{\"label\":\"Parkinson's disease 7\",\"id\":\"DOID:0060370\"}]" }, { "gene_id": 57339, "description": "junctophilin 1", "gene_symbol": "[\"Jph1\"]", "do": null }, { "gene_id": 57342, "description": "parvin, alpha", "gene_symbol": "[\"Parva\"]", "do": null }, { "gene_id": 57357, "description": "steroid 5 alpha-reductase 3", "gene_symbol": "[\"Srd5a3\"]", "do": null }, { "gene_id": 57370, "description": "UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 3", "gene_symbol": "[\"B4galt3\"]", "do": null }, { "gene_id": 57377, "description": "mannosyl-oligosaccharide glucosidase", "gene_symbol": "[\"Mogs\"]", "do": null }, { "gene_id": 57385, "description": "pyrimidinergic receptor P2Y, G-protein coupled, 4", "gene_symbol": "[\"P2ry4\"]", "do": null }, { "gene_id": 57394, "description": "collectrin, amino acid transport regulator", "gene_symbol": "[\"Cltrn\"]", "do": null }, { "gene_id": 57423, "description": "ATP synthase membrane subunit f", "gene_symbol": "[\"Atp5mf\"]", "do": null }, { "gene_id": 57435, "description": "perilipin 4", "gene_symbol": "[\"Plin4\"]", "do": null }, { "gene_id": 57436, "description": "GABA type A receptor associated protein like 1", "gene_symbol": "[\"Gabarapl1\"]", "do": null }, { "gene_id": 57442, "description": "potassium voltage-gated channel, Isk-related subfamily, gene 3", "gene_symbol": "[\"Kcne3\"]", "do": null }, { "gene_id": 57738, "description": "solute carrier family 15 (H+/peptide transporter), member 2", "gene_symbol": "[\"Slc15a2\"]", "do": null }, { "gene_id": 57742, "description": "abhydrolase domain containing 1", "gene_symbol": "[\"Abhd1\"]", "do": null }, { "gene_id": 57757, "description": "peptidoglycan recognition protein 2", "gene_symbol": "[\"Pglyrp2\"]", "do": null }, { "gene_id": 57764, "description": "netrin 4", "gene_symbol": "[\"Ntn4\"]", "do": null }, { "gene_id": 57773, "description": "WD repeat domain 4", "gene_symbol": "[\"Wdr4\"]", "do": null }, { "gene_id": 57776, "description": "tweety family member 1", "gene_symbol": "[\"Ttyh1\"]", "do": null }, { "gene_id": 57780, "description": "FXYD domain-containing ion transport regulator 7", "gene_symbol": "[\"Fxyd7\"]", "do": null }, { "gene_id": 57781, "description": "CD200 receptor 1", "gene_symbol": "[\"Cd200r1\"]", "do": null }, { "gene_id": 57783, "description": "TNFAIP3 interacting protein 1", "gene_symbol": "[\"Tnip1\"]", "do": null }, { "gene_id": 57808, "description": "ribosomal protein L35A", "gene_symbol": "[\"Rpl35a\"]", "do": null }, { "gene_id": 57810, "description": "cell adhesion associated, oncogene regulated", "gene_symbol": "[\"Cdon\"]", "do": "[{\"label\":\"holoprosencephaly 11\",\"id\":\"DOID:0110877\"}]" }, { "gene_id": 57814, "description": "potassium voltage-gated channel, Isk-related subfamily, gene 4", "gene_symbol": "[\"Kcne4\"]", "do": null }, { "gene_id": 57874, "description": "3-hydroxyacyl-CoA dehydratase 3", "gene_symbol": "[\"Hacd3\"]", "do": null }, { "gene_id": 57875, "description": "angiopoietin-like 4", "gene_symbol": "[\"Angptl4\"]", "do": null }, { "gene_id": 57890, "description": "interleukin 17 receptor E", "gene_symbol": "[\"Il17re\"]", "do": null }, { "gene_id": 57895, "description": "coiled-coil domain containing 126", "gene_symbol": "[\"Ccdc126\"]", "do": null }, { "gene_id": 57908, "description": "zinc finger protein 318", "gene_symbol": "[\"Zfp318\"]", "do": null }, { "gene_id": 57914, "description": "cytokine receptor-like factor 2", "gene_symbol": "[\"Crlf2\"]", "do": null }, { "gene_id": 58170, "description": "acid-sensing ion channel family member 5", "gene_symbol": "[\"Asic5\"]", "do": null }, { "gene_id": 58176, "description": "Rhesus blood group-associated B glycoprotein", "gene_symbol": "[\"Rhbg\"]", "do": null }, { "gene_id": 58178, "description": "sortilin-related VPS10 domain containing receptor 1", "gene_symbol": "[\"Sorcs1\"]", "do": null }, { "gene_id": 58182, "description": "prokineticin receptor 1", "gene_symbol": "[\"Prokr1\"]", "do": null }, { "gene_id": 58193, "description": "exostosin-like glycosyltransferase 2", "gene_symbol": "[\"Extl2\"]", "do": null }, { "gene_id": 58200, "description": "protein phosphatase 1, regulatory inhibitor subunit 1A", "gene_symbol": "[\"Ppp1r1a\"]", "do": null }, { "gene_id": 58203, "description": "Z-DNA binding protein 1", "gene_symbol": "[\"Zbp1\"]", "do": null }, { "gene_id": 58205, "description": "programmed cell death 1 ligand 2", "gene_symbol": "[\"Pdcd1lg2\"]", "do": null }, { "gene_id": 58207, "description": "solute carrier family 43, member 3", "gene_symbol": "[\"Slc43a3\"]", "do": null }, { "gene_id": 58217, "description": "triggering receptor expressed on myeloid cells 1", "gene_symbol": "[\"Trem1\"]", "do": null }, { "gene_id": 58218, "description": "triggering receptor expressed on myeloid cells 3", "gene_symbol": "[\"Trem3\"]", "do": null }, { "gene_id": 58223, "description": "matrix metallopeptidase 19", "gene_symbol": "[\"Mmp19\"]", "do": null }, { "gene_id": 58234, "description": "SH3 and multiple ankyrin repeat domains 3", "gene_symbol": "[\"Shank3\"]", "do": "[{\"label\":\"Phelan-McDermid syndrome\",\"id\":\"DOID:0080354\"},{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 58235, "description": "nectin cell adhesion molecule 1", "gene_symbol": "[\"Nectin1\"]", "do": null }, { "gene_id": 58237, "description": "Na+/K+ transporting ATPase interacting 4", "gene_symbol": "[\"Nkain4\"]", "do": null }, { "gene_id": 58245, "description": "G protein-coupled receptor 180", "gene_symbol": "[\"Gpr180\"]", "do": null }, { "gene_id": 58250, "description": "carbohydrate sulfotransferase 11", "gene_symbol": "[\"Chst11\"]", "do": null }, { "gene_id": 58802, "description": "potassium large conductance calcium-activated channel, subfamily M, beta member 4", "gene_symbol": "[\"Kcnmb4\"]", "do": null }, { "gene_id": 58805, "description": "MLX interacting protein-like", "gene_symbol": "[\"Mlxipl\"]", "do": "[{\"label\":\"irritable bowel syndrome\",\"id\":\"DOID:9778\"}]" }, { "gene_id": 58807, "description": "solute carrier organic anion transporter family, member 1c1", "gene_symbol": "[\"Slco1c1\"]", "do": null }, { "gene_id": 58810, "description": "aldo-keto reductase family 1, member A1", "gene_symbol": "[\"Akr1a1\"]", "do": null }, { "gene_id": 58859, "description": "epidermal growth factor-containing fibulin-like extracellular matrix protein 2", "gene_symbol": "[\"Efemp2\"]", "do": "[{\"label\":\"aortic aneurysm\",\"id\":\"DOID:3627\"},{\"label\":\"cutis laxa\",\"id\":\"DOID:3144\"}]" }, { "gene_id": 58860, "description": "ADAM-like, decysin 1", "gene_symbol": "[\"Adamdec1\"]", "do": null }, { "gene_id": 58861, "description": "cysteinyl leukotriene receptor 1", "gene_symbol": "[\"Cysltr1\"]", "do": null }, { "gene_id": 58866, "description": "trehalase (brush-border membrane glycoprotein)", "gene_symbol": "[\"Treh\"]", "do": null }, { "gene_id": 58875, "description": "3-hydroxyisobutyrate dehydrogenase", "gene_symbol": "[\"Hibadh\"]", "do": null }, { "gene_id": 58911, "description": "sulfatase modifying factor 1", "gene_symbol": "[\"Sumf1\"]", "do": "[{\"label\":\"mucosulfatidosis\",\"id\":\"DOID:0050441\"}]" }, { "gene_id": 58992, "description": "coagulation factor XII (Hageman factor)", "gene_symbol": "[\"F12\"]", "do": "[{\"label\":\"factor XII deficiency\",\"id\":\"DOID:2231\"}]" }, { "gene_id": 58996, "description": "Rho GTPase activating protein 23", "gene_symbol": "[\"Arhgap23\"]", "do": null }, { "gene_id": 58998, "description": "nectin cell adhesion molecule 3", "gene_symbol": "[\"Nectin3\"]", "do": null }, { "gene_id": 59006, "description": "myozenin 2", "gene_symbol": "[\"Myoz2\"]", "do": null }, { "gene_id": 59009, "description": "SH3 domain containing ring finger 1", "gene_symbol": "[\"Sh3rf1\"]", "do": null }, { "gene_id": 59010, "description": "sulfide quinone oxidoreductase", "gene_symbol": "[\"Sqor\"]", "do": null }, { "gene_id": 59012, "description": "monooxygenase, DBH-like 1", "gene_symbol": "[\"Moxd1\"]", "do": null }, { "gene_id": 59013, "description": "heterogeneous nuclear ribonucleoprotein H1", "gene_symbol": "[\"Hnrnph1\"]", "do": null }, { "gene_id": 59021, "description": "RAB2A, member RAS oncogene family", "gene_symbol": "[\"Rab2a\"]", "do": null }, { "gene_id": 59025, "description": "ubiquitin specific peptidase 14", "gene_symbol": "[\"Usp14\"]", "do": null }, { "gene_id": 59026, "description": "HECT, UBA and WWE domain containing 1", "gene_symbol": "[\"Huwe1\"]", "do": null }, { "gene_id": 59027, "description": "nicotinamide phosphoribosyltransferase", "gene_symbol": "[\"Nampt\"]", "do": null }, { "gene_id": 59031, "description": "carbohydrate sulfotransferase 12", "gene_symbol": "[\"Chst12\"]", "do": null }, { "gene_id": 59033, "description": "solute carrier family 4 (anion exchanger), member 8", "gene_symbol": "[\"Slc4a8\"]", "do": null }, { "gene_id": 59035, "description": "coactivator-associated arginine methyltransferase 1", "gene_symbol": "[\"Carm1\"]", "do": null }, { "gene_id": 59038, "description": "peroxisomal membrane protein 4", "gene_symbol": "[\"Pxmp4\"]", "do": null }, { "gene_id": 59044, "description": "ring finger protein 130", "gene_symbol": "[\"Rnf130\"]", "do": null }, { "gene_id": 59045, "description": "StAR related lipid transfer domain containing 3", "gene_symbol": "[\"Stard3\"]", "do": null }, { "gene_id": 59048, "description": "C1GALT1-specific chaperone 1", "gene_symbol": "[\"C1galt1c1\"]", "do": null }, { "gene_id": 59052, "description": "methyltransferase like 9", "gene_symbol": "[\"Mettl9\"]", "do": null }, { "gene_id": 59056, "description": "EvC ciliary complex subunit 1", "gene_symbol": "[\"Evc\"]", "do": "[{\"label\":\"Ellis-Van Creveld syndrome\",\"id\":\"DOID:12714\"}]" }, { "gene_id": 59079, "description": "Erbb2 interacting protein", "gene_symbol": "[\"Erbin\"]", "do": null }, { "gene_id": 59083, "description": "fetuin beta", "gene_symbol": "[\"Fetub\"]", "do": null }, { "gene_id": 59090, "description": "midnolin", "gene_symbol": "[\"Midn\"]", "do": null }, { "gene_id": 59091, "description": "junctophilin 2", "gene_symbol": "[\"Jph2\"]", "do": null }, { "gene_id": 59093, "description": "poly(rC) binding protein 3", "gene_symbol": "[\"Pcbp3\"]", "do": null }, { "gene_id": 59125, "description": "NIMA (never in mitosis gene a)-related expressed kinase 7", "gene_symbol": "[\"Nek7\"]", "do": null }, { "gene_id": 59287, "description": "nicastrin", "gene_symbol": "[\"Ncstn\"]", "do": "[{\"label\":\"chronic myeloid leukemia\",\"id\":\"DOID:8552\"},{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"},{\"label\":\"urinary bladder cancer\",\"id\":\"DOID:11054\"}]" }, { "gene_id": 59289, "description": "atypical chemokine receptor 2", "gene_symbol": "[\"Ackr2\"]", "do": null }, { "gene_id": 59290, "description": "glycoprotein A33 transmembrane", "gene_symbol": "[\"Gpa33\"]", "do": null }, { "gene_id": 59308, "description": "endomucin", "gene_symbol": "[\"Emcn\"]", "do": null }, { "gene_id": 60315, "description": "melanocyte proliferating gene 1", "gene_symbol": "[\"Myg1\"]", "do": null }, { "gene_id": 60322, "description": "carbohydrate sulfotransferase 7", "gene_symbol": "[\"Chst7\"]", "do": null }, { "gene_id": 60367, "description": "interleukin 1 receptor accessory protein-like 2", "gene_symbol": "[\"Il1rapl2\"]", "do": null }, { "gene_id": 60455, "description": "post-glycosylphosphatidylinositol attachment to proteins 6", "gene_symbol": "[\"Pgap6\"]", "do": null }, { "gene_id": 60504, "description": "interleukin 21 receptor", "gene_symbol": "[\"Il21r\"]", "do": null }, { "gene_id": 60505, "description": "interleukin 21", "gene_symbol": "[\"Il21\"]", "do": null }, { "gene_id": 60507, "description": "queuine tRNA-ribosyltransferase catalytic subunit 1", "gene_symbol": "[\"Qtrt1\"]", "do": null }, { "gene_id": 60532, "description": "WT1 associating protein", "gene_symbol": "[\"Wtap\"]", "do": null }, { "gene_id": 60533, "description": "CD274 antigen", "gene_symbol": "[\"Cd274\"]", "do": null }, { "gene_id": 60595, "description": "actinin alpha 4", "gene_symbol": "[\"Actn4\"]", "do": "[{\"label\":\"focal segmental glomerulosclerosis 1\",\"id\":\"DOID:0111128\"}]" }, { "gene_id": 60596, "description": "guanylate cyclase 1, soluble, alpha 1", "gene_symbol": "[\"Gucy1a1\"]", "do": "[{\"label\":\"primary open angle glaucoma\",\"id\":\"DOID:1070\"}]" }, { "gene_id": 63859, "description": "interphotoreceptor matrix proteoglycan 1", "gene_symbol": "[\"Impg1\"]", "do": null }, { "gene_id": 63873, "description": "transient receptor potential cation channel, subfamily V, member 4", "gene_symbol": "[\"Trpv4\"]", "do": "[{\"label\":\"autosomal dominant nonsyndromic deafness 25\",\"id\":\"DOID:0110555\"}]" }, { "gene_id": 63958, "description": "ubiquitination factor E4B", "gene_symbol": "[\"Ube4b\"]", "do": null }, { "gene_id": 63959, "description": "solute carrier family 29 (nucleoside transporters), member 1", "gene_symbol": "[\"Slc29a1\"]", "do": "[{\"label\":\"alcohol dependence\",\"id\":\"DOID:0050741\"},{\"label\":\"diffuse idiopathic skeletal hyperostosis\",\"id\":\"DOID:6652\"}]" }, { "gene_id": 63993, "description": "solute carrier family 5 (choline transporter), member 7", "gene_symbol": "[\"Slc5a7\"]", "do": null }, { "gene_id": 64009, "description": "spectrin repeat containing, nuclear envelope 1", "gene_symbol": "[\"Syne1\"]", "do": "[{\"label\":\"Emery-Dreifuss muscular dystrophy\",\"id\":\"DOID:11726\"}]" }, { "gene_id": 64051, "description": "synaptic vesicle glycoprotein 2a", "gene_symbol": "[\"Sv2a\"]", "do": null }, { "gene_id": 64074, "description": "SPARC related modular calcium binding 2", "gene_symbol": "[\"Smoc2\"]", "do": null }, { "gene_id": 64075, "description": "SPARC related modular calcium binding 1", "gene_symbol": "[\"Smoc1\"]", "do": "[{\"label\":\"microphthalmia with limb anomalies\",\"id\":\"DOID:0060861\"}]" }, { "gene_id": 64082, "description": "popeye domain containing 2", "gene_symbol": "[\"Popdc2\"]", "do": null }, { "gene_id": 64085, "description": "calsyntenin 2", "gene_symbol": "[\"Clstn2\"]", "do": null }, { "gene_id": 64095, "description": "G protein-coupled receptor 35", "gene_symbol": "[\"Gpr35\"]", "do": null }, { "gene_id": 64103, "description": "tenomodulin", "gene_symbol": "[\"Tnmd\"]", "do": null }, { "gene_id": 64138, "description": "cathepsin Z", "gene_symbol": "[\"Ctsz\"]", "do": null }, { "gene_id": 64139, "description": "cathepsin M", "gene_symbol": "[\"Ctsm\"]", "do": null }, { "gene_id": 64176, "description": "synaptic vesicle glycoprotein 2b", "gene_symbol": "[\"Sv2b\"]", "do": null }, { "gene_id": 64177, "description": "transient receptor potential cation channel, subfamily V, member 6", "gene_symbol": "[\"Trpv6\"]", "do": null }, { "gene_id": 64213, "description": "suppression of tumorigenicity 7", "gene_symbol": "[\"St7\"]", "do": null }, { "gene_id": 64294, "description": "integral membrane protein 2C", "gene_symbol": "[\"Itm2c\"]", "do": null }, { "gene_id": 64297, "description": "G protein-coupled receptor, family C, group 5, member B", "gene_symbol": "[\"Gprc5b\"]", "do": null }, { "gene_id": 64339, "description": "fibronectin type III domain containing 4", "gene_symbol": "[\"Fndc4\"]", "do": null }, { "gene_id": 64378, "description": "G-protein coupled receptor 88", "gene_symbol": "[\"Gpr88\"]", "do": null }, { "gene_id": 64379, "description": "Iroquois homeobox 6", "gene_symbol": "[\"Irx6\"]", "do": null }, { "gene_id": 64383, "description": "sirtuin 2", "gene_symbol": "[\"Sirt2\"]", "do": null }, { "gene_id": 64435, "description": "Fc receptor, IgA, IgM, high affinity", "gene_symbol": "[\"Fcamr\"]", "do": null }, { "gene_id": 64450, "description": "G protein-coupled receptor 85", "gene_symbol": "[\"Gpr85\"]", "do": null }, { "gene_id": 64451, "description": "disco interacting protein 2 homolog A", "gene_symbol": "[\"Dip2a\"]", "do": null }, { "gene_id": 64452, "description": "solute carrier family 5, member 4a", "gene_symbol": "[\"Slc5a4a\"]", "do": null }, { "gene_id": 64540, "description": "tetraspanin 4", "gene_symbol": "[\"Tspan4\"]", "do": null }, { "gene_id": 64580, "description": "N-deacetylase/N-sulfotransferase (heparin glucosaminyl) 4", "gene_symbol": "[\"Ndst4\"]", "do": null }, { "gene_id": 64652, "description": "nischarin", "gene_symbol": "[\"Nisch\"]", "do": null }, { "gene_id": 64654, "description": "fibroblast growth factor 23", "gene_symbol": "[\"Fgf23\"]", "do": "[{\"label\":\"autosomal dominant hypophosphatemic rickets\",\"id\":\"DOID:0050948\"}]" }, { "gene_id": 64705, "description": "dihydropyrimidinase", "gene_symbol": "[\"Dpys\"]", "do": null }, { "gene_id": 64706, "description": "signal peptide, CUB domain, EGF-like 1", "gene_symbol": "[\"Scube1\"]", "do": null }, { "gene_id": 64817, "description": "sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1", "gene_symbol": "[\"Svep1\"]", "do": null }, { "gene_id": 64930, "description": "TSC complex subunit 1", "gene_symbol": "[\"Tsc1\"]", "do": "[{\"label\":\"anterior segment dysgenesis\",\"id\":\"DOID:0060648\"},{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"autosomal recessive polycystic kidney disease\",\"id\":\"DOID:0110861\"},{\"label\":\"spinal disease\",\"id\":\"DOID:0060564\"},{\"label\":\"tuberous sclerosis\",\"id\":\"DOID:13515\"}]" }, { "gene_id": 64931, "description": "IZUMO1 receptor, JUNO", "gene_symbol": "[\"Izumo1r\"]", "do": null }, { "gene_id": 64945, "description": "claudin 12", "gene_symbol": "[\"Cldn12\"]", "do": null }, { "gene_id": 65020, "description": "zinc finger protein 110", "gene_symbol": "[\"Zfp110\"]", "do": null }, { "gene_id": 65079, "description": "reticulon 4 receptor", "gene_symbol": "[\"Rtn4r\"]", "do": null }, { "gene_id": 65086, "description": "lysophosphatidic acid receptor 3", "gene_symbol": "[\"Lpar3\"]", "do": null }, { "gene_id": 65100, "description": "zinc finger protein of the cerebellum 5", "gene_symbol": "[\"Zic5\"]", "do": null }, { "gene_id": 65107, "description": "low-density lipoprotein receptor-related protein 10", "gene_symbol": "[\"Lrp10\"]", "do": null }, { "gene_id": 65112, "description": "prostate transmembrane protein, androgen induced 1", "gene_symbol": "[\"Pmepa1\"]", "do": null }, { "gene_id": 65221, "description": "solute carrier family 15, member 3", "gene_symbol": "[\"Slc15a3\"]", "do": null }, { "gene_id": 65246, "description": "exportin 7", "gene_symbol": "[\"Xpo7\"]", "do": null }, { "gene_id": 65254, "description": "dihydropyrimidinase-like 5", "gene_symbol": "[\"Dpysl5\"]", "do": null }, { "gene_id": 65945, "description": "calsyntenin 1", "gene_symbol": "[\"Clstn1\"]", "do": null }, { "gene_id": 65960, "description": "twisted gastrulation BMP signaling modulator 1", "gene_symbol": "[\"Twsg1\"]", "do": null }, { "gene_id": 65969, "description": "cubilin", "gene_symbol": "[\"Cubn\"]", "do": null }, { "gene_id": 65970, "description": "LIM domain and actin binding 1", "gene_symbol": "[\"Lima1\"]", "do": null }, { "gene_id": 65972, "description": "interferon gamma inducible protein 30", "gene_symbol": "[\"Ifi30\"]", "do": null }, { "gene_id": 65973, "description": "aspartate-beta-hydroxylase", "gene_symbol": "[\"Asph\"]", "do": null }, { "gene_id": 66042, "description": "sclerostin domain containing 1", "gene_symbol": "[\"Sostdc1\"]", "do": null }, { "gene_id": 66052, "description": "succinate dehydrogenase complex, subunit C, integral membrane protein", "gene_symbol": "[\"Sdhc\"]", "do": "[{\"label\":\"Leigh disease\",\"id\":\"DOID:3652\"}]" }, { "gene_id": 66065, "description": "hydroxysteroid (17-beta) dehydrogenase 14", "gene_symbol": "[\"Hsd17b14\"]", "do": null }, { "gene_id": 66073, "description": "thioredoxin domain containing 12 (endoplasmic reticulum)", "gene_symbol": "[\"Txndc12\"]", "do": null }, { "gene_id": 66074, "description": "transmembrane protein 167", "gene_symbol": "[\"Tmem167\"]", "do": null }, { "gene_id": 66075, "description": "coiled-coil-helix-coiled-coil-helix domain containing 3", "gene_symbol": "[\"Chchd3\"]", "do": null }, { "gene_id": 66078, "description": "tRNA splicing endonuclease subunit 34", "gene_symbol": "[\"Tsen34\"]", "do": null }, { "gene_id": 66085, "description": "eukaryotic translation initiation factor 3, subunit F", "gene_symbol": "[\"Eif3f\"]", "do": null }, { "gene_id": 66098, "description": "coiled-coil-helix-coiled-coil-helix domain containing 6", "gene_symbol": "[\"Chchd6\"]", "do": null }, { "gene_id": 66104, "description": "transcription elongation factor A (SII)-like 6", "gene_symbol": "[\"Tceal6\"]", "do": null }, { "gene_id": 66108, "description": "NADH:ubiquinone oxidoreductase subunit A9", "gene_symbol": "[\"Ndufa9\"]", "do": null }, { "gene_id": 66109, "description": "tetraspanin 13", "gene_symbol": "[\"Tspan13\"]", "do": null }, { "gene_id": 66112, "description": "mitochondrial amidoxime reducing component 1", "gene_symbol": "[\"Mtarc1\"]", "do": null }, { "gene_id": 66118, "description": "SAP domain containing ribonucleoprotein", "gene_symbol": "[\"Sarnp\"]", "do": null }, { "gene_id": 66146, "description": "macoilin 1", "gene_symbol": "[\"Maco1\"]", "do": null }, { "gene_id": 66171, "description": "6-phosphogluconolactonase", "gene_symbol": "[\"Pgls\"]", "do": null }, { "gene_id": 66179, "description": "2-oxoglutarate and iron-dependent oxygenase domain containing 3", "gene_symbol": "[\"Ogfod3\"]", "do": null }, { "gene_id": 66180, "description": "prolyl 3-hydroxylase family member 4 (non-enzymatic)", "gene_symbol": "[\"P3h4\"]", "do": null }, { "gene_id": 66185, "description": "vir like m6A methyltransferase associated", "gene_symbol": "[\"Virma\"]", "do": null }, { "gene_id": 66205, "description": "CD302 antigen", "gene_symbol": "[\"Cd302\"]", "do": null }, { "gene_id": 66212, "description": "SEC61 translocon subunit beta", "gene_symbol": "[\"Sec61b\"]", "do": null }, { "gene_id": 66240, "description": "potassium voltage-gated channel subfamily E regulatory subunit 5", "gene_symbol": "[\"Kcne5\"]", "do": null }, { "gene_id": 66241, "description": "transmembrane protein 9", "gene_symbol": "[\"Tmem9\"]", "do": null }, { "gene_id": 66245, "description": "HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1", "gene_symbol": "[\"Hspbp1\"]", "do": null }, { "gene_id": 66248, "description": "ALG5 dolichyl-phosphate beta-glucosyltransferase", "gene_symbol": "[\"Alg5\"]", "do": null }, { "gene_id": 66254, "description": "DIM1 rRNA methyltransferase and ribosome maturation factor", "gene_symbol": "[\"Dimt1\"]", "do": null }, { "gene_id": 66256, "description": "signal sequence receptor, beta", "gene_symbol": "[\"Ssr2\"]", "do": null }, { "gene_id": 66269, "description": "transmembrane p24 trafficking protein 6", "gene_symbol": "[\"Tmed6\"]", "do": null }, { "gene_id": 66289, "description": "mucosal pentraxin 1", "gene_symbol": "[\"Mptx1\"]", "do": null }, { "gene_id": 66294, "description": "FAM3 metabolism regulating signaling molecule A", "gene_symbol": "[\"Fam3a\"]", "do": null }, { "gene_id": 66314, "description": "tumor protein D52-like 2", "gene_symbol": "[\"Tpd52l2\"]", "do": null }, { "gene_id": 66315, "description": "SUMO1/sentrin specific peptidase 7", "gene_symbol": "[\"Senp7\"]", "do": null }, { "gene_id": 66335, "description": "ATPase, H+ transporting, lysosomal V1 subunit C1", "gene_symbol": "[\"Atp6v1c1\"]", "do": null }, { "gene_id": 66354, "description": "SNW domain containing 1", "gene_symbol": "[\"Snw1\"]", "do": null }, { "gene_id": 66358, "description": "ADP-ribose/CDP-alcohol diphosphatase, manganese dependent", "gene_symbol": "[\"Adprm\"]", "do": null }, { "gene_id": 66366, "description": "ERGIC and golgi 3", "gene_symbol": "[\"Ergic3\"]", "do": null }, { "gene_id": 66367, "description": "RIKEN cDNA 2310022A10 gene", "gene_symbol": "[\"2310022A10Rik\"]", "do": null }, { "gene_id": 66368, "description": "RNA 3'-terminal phosphate cyclase", "gene_symbol": "[\"Rtca\"]", "do": null }, { "gene_id": 66374, "description": "RIKEN cDNA 2310011J03 gene", "gene_symbol": "[\"2310011J03Rik\"]", "do": null }, { "gene_id": 66375, "description": "dehydrogenase/reductase 7", "gene_symbol": "[\"Dhrs7\"]", "do": null }, { "gene_id": 66385, "description": "protein phosphatase 1, regulatory subunit 7", "gene_symbol": "[\"Ppp1r7\"]", "do": null }, { "gene_id": 66395, "description": "AHNAK nucleoprotein", "gene_symbol": "[\"Ahnak\"]", "do": null }, { "gene_id": 66407, "description": "mitochondrial ribosomal protein S15", "gene_symbol": "[\"Mrps15\"]", "do": null }, { "gene_id": 66409, "description": "ribosomal L1 domain containing 1", "gene_symbol": "[\"Rsl1d1\"]", "do": null }, { "gene_id": 66416, "description": "NADH:ubiquinone oxidoreductase subunit A7", "gene_symbol": "[\"Ndufa7\"]", "do": null }, { "gene_id": 66435, "description": "UDP-glucose glycoprotein glucosyltransferase 2", "gene_symbol": "[\"Uggt2\"]", "do": null }, { "gene_id": 66445, "description": "cytochrome c-1", "gene_symbol": "[\"Cyc1\"]", "do": null }, { "gene_id": 66451, "description": "RIKEN cDNA 2610528J11 gene", "gene_symbol": "[\"2610528J11Rik\"]", "do": null }, { "gene_id": 66494, "description": "PRELI domain containing 1", "gene_symbol": "[\"Prelid1\"]", "do": null }, { "gene_id": 66513, "description": "TGF-beta activated kinase 1/MAP3K7 binding protein 1", "gene_symbol": "[\"Tab1\"]", "do": null }, { "gene_id": 66552, "description": "signal peptide peptidase like 2A", "gene_symbol": "[\"Sppl2a\"]", "do": null }, { "gene_id": 66557, "description": "BPI fold containing family B, member 2", "gene_symbol": "[\"Bpifb2\"]", "do": null }, { "gene_id": 66596, "description": "general transcription factor III A", "gene_symbol": "[\"Gtf3a\"]", "do": null }, { "gene_id": 66601, "description": "transmembrane and immunoglobulin domain containing 1", "gene_symbol": "[\"Tmigd1\"]", "do": null }, { "gene_id": 66615, "description": "autophagy related 4B, cysteine peptidase", "gene_symbol": "[\"Atg4b\"]", "do": null }, { "gene_id": 66631, "description": "solute carrier family 71 member 2", "gene_symbol": "[\"Slc71a2\"]", "do": null }, { "gene_id": 66646, "description": "ribulose-5-phosphate-3-epimerase", "gene_symbol": "[\"Rpe\"]", "do": null }, { "gene_id": 66647, "description": "NSE3 homolog, SMC5-SMC6 complex component", "gene_symbol": "[\"Nsmce3\"]", "do": null }, { "gene_id": 66650, "description": "nephrocan", "gene_symbol": "[\"Nepn\"]", "do": null }, { "gene_id": 66660, "description": "SAFB-like, transcription modulator", "gene_symbol": "[\"Sltm\"]", "do": null }, { "gene_id": 66667, "description": "Hspb associated protein 1", "gene_symbol": "[\"Hspbap1\"]", "do": null }, { "gene_id": 66673, "description": "sortilin-related VPS10 domain containing receptor 3", "gene_symbol": "[\"Sorcs3\"]", "do": null }, { "gene_id": 66676, "description": "transmembrane p24 trafficking protein 7", "gene_symbol": "[\"Tmed7\"]", "do": null }, { "gene_id": 66681, "description": "phosphoglucomutase 2", "gene_symbol": "[\"Pgm2\"]", "do": null }, { "gene_id": 66686, "description": "discoidin, CUB and LCCL domain containing 1", "gene_symbol": "[\"Dcbld1\"]", "do": null }, { "gene_id": 66687, "description": "TBC1 domain family, member 15", "gene_symbol": "[\"Tbc1d15\"]", "do": null }, { "gene_id": 66691, "description": "GTPase activating protein and VPS9 domains 1", "gene_symbol": "[\"Gapvd1\"]", "do": null }, { "gene_id": 66695, "description": "asporin", "gene_symbol": "[\"Aspn\"]", "do": null }, { "gene_id": 66712, "description": "sperm equatorial segment protein 1", "gene_symbol": "[\"Spesp1\"]", "do": null }, { "gene_id": 66713, "description": "actin related protein 2", "gene_symbol": "[\"Actr2\"]", "do": null }, { "gene_id": 66724, "description": "TGF-beta activated kinase 1/MAP3K7 binding protein 3", "gene_symbol": "[\"Tab3\"]", "do": null }, { "gene_id": 66725, "description": "leucine-rich repeat kinase 2", "gene_symbol": "[\"Lrrk2\"]", "do": null }, { "gene_id": 66743, "description": "ring finger protein 220", "gene_symbol": "[\"Rnf220\"]", "do": null }, { "gene_id": 66753, "description": "endoplasmic reticulum lectin 1", "gene_symbol": "[\"Erlec1\"]", "do": null }, { "gene_id": 66784, "description": "family with sequence similarity 187, member A", "gene_symbol": "[\"Fam187a\"]", "do": null }, { "gene_id": 66789, "description": "asparagine-linked glycosylation 14", "gene_symbol": "[\"Alg14\"]", "do": null }, { "gene_id": 66797, "description": "contactin associated protein-like 2", "gene_symbol": "[\"Cntnap2\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"cortical dysplasia-focal epilepsy syndrome\",\"id\":\"DOID:0090130\"}]" }, { "gene_id": 66805, "description": "tetraspanin 1", "gene_symbol": "[\"Tspan1\"]", "do": null }, { "gene_id": 66811, "description": "dual oxidase maturation factor 2", "gene_symbol": "[\"Duoxa2\"]", "do": null }, { "gene_id": 66817, "description": "transmembrane protein 170", "gene_symbol": "[\"Tmem170\"]", "do": null }, { "gene_id": 66834, "description": "acyl-CoA thioesterase 13", "gene_symbol": "[\"Acot13\"]", "do": null }, { "gene_id": 66836, "description": "transmembrane protein 223", "gene_symbol": "[\"Tmem223\"]", "do": null }, { "gene_id": 66840, "description": "WD repeat domain 45B", "gene_symbol": "[\"Wdr45b\"]", "do": null }, { "gene_id": 66841, "description": "electron transferring flavoprotein, dehydrogenase", "gene_symbol": "[\"Etfdh\"]", "do": null }, { "gene_id": 66848, "description": "fucosidase, alpha-L- 2, plasma", "gene_symbol": "[\"Fuca2\"]", "do": null }, { "gene_id": 66849, "description": "protein phosphatase 1, regulatory inhibitor subunit 2", "gene_symbol": "[\"Ppp1r2\"]", "do": null }, { "gene_id": 66853, "description": "patatin-like phospholipase domain containing 2", "gene_symbol": "[\"Pnpla2\"]", "do": null }, { "gene_id": 66857, "description": "phospholipase B domain containing 1", "gene_symbol": "[\"Plbd1\"]", "do": null }, { "gene_id": 66860, "description": "tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1", "gene_symbol": "[\"Tanc1\"]", "do": null }, { "gene_id": 66861, "description": "DnaJ heat shock protein family (Hsp40) member C10", "gene_symbol": "[\"Dnajc10\"]", "do": null }, { "gene_id": 66864, "description": "C-type lectin domain family 14, member a", "gene_symbol": "[\"Clec14a\"]", "do": null }, { "gene_id": 66865, "description": "peptidase (mitochondrial processing) alpha", "gene_symbol": "[\"Pmpca\"]", "do": null }, { "gene_id": 66873, "description": "TLR4 interactor with leucine-rich repeats", "gene_symbol": "[\"Tril\"]", "do": null }, { "gene_id": 66874, "description": "nuclear cap binding subunit 3", "gene_symbol": "[\"Ncbp3\"]", "do": null }, { "gene_id": 66881, "description": "prenylcysteine oxidase 1", "gene_symbol": "[\"Pcyox1\"]", "do": null }, { "gene_id": 66889, "description": "ring finger protein 128", "gene_symbol": "[\"Rnf128\"]", "do": null }, { "gene_id": 66890, "description": "lectin, mannose-binding 2", "gene_symbol": "[\"Lman2\"]", "do": null }, { "gene_id": 66894, "description": "WW domain containing E3 ubiquitin protein ligase 2", "gene_symbol": "[\"Wwp2\"]", "do": null }, { "gene_id": 66898, "description": "BAI1-associated protein 2-like 1", "gene_symbol": "[\"Baiap2l1\"]", "do": null }, { "gene_id": 66899, "description": "factor interacting with PAPOLA and CPSF1", "gene_symbol": "[\"Fip1l1\"]", "do": null }, { "gene_id": 66901, "description": "protein Z, vitamin K-dependent plasma glycoprotein", "gene_symbol": "[\"Proz\"]", "do": null }, { "gene_id": 66902, "description": "methylthioadenosine phosphorylase", "gene_symbol": "[\"Mtap\"]", "do": null }, { "gene_id": 66904, "description": "propionyl Coenzyme A carboxylase, beta polypeptide", "gene_symbol": "[\"Pccb\"]", "do": null }, { "gene_id": 66905, "description": "perilipin 3", "gene_symbol": "[\"Plin3\"]", "do": null }, { "gene_id": 66910, "description": "transmembrane protein 107", "gene_symbol": "[\"Tmem107\"]", "do": null }, { "gene_id": 66938, "description": "manchette microtubule inner protein 1", "gene_symbol": "[\"Mnmip1\"]", "do": null }, { "gene_id": 66940, "description": "shisa family member 5", "gene_symbol": "[\"Shisa5\"]", "do": null }, { "gene_id": 66942, "description": "DEAD box helicase 18", "gene_symbol": "[\"Ddx18\"]", "do": null }, { "gene_id": 66950, "description": "proton activated chloride channel 1", "gene_symbol": "[\"Pacc1\"]", "do": null }, { "gene_id": 66967, "description": "ER degradation enhancer, mannosidase alpha-like 3", "gene_symbol": "[\"Edem3\"]", "do": null }, { "gene_id": 66970, "description": "single-stranded DNA binding protein 2", "gene_symbol": "[\"Ssbp2\"]", "do": null }, { "gene_id": 67003, "description": "ubiquinol cytochrome c reductase core protein 2", "gene_symbol": "[\"Uqcrc2\"]", "do": null }, { "gene_id": 67010, "description": "RNA binding motif protein 7", "gene_symbol": "[\"Rbm7\"]", "do": null }, { "gene_id": 67013, "description": "OMA1 zinc metallopeptidase", "gene_symbol": "[\"Oma1\"]", "do": null }, { "gene_id": 67027, "description": "makorin, ring finger protein, 2", "gene_symbol": "[\"Mkrn2\"]", "do": null }, { "gene_id": 67039, "description": "RNA binding motif protein 25", "gene_symbol": "[\"Rbm25\"]", "do": null }, { "gene_id": 67052, "description": "NDC80 kinetochore complex component", "gene_symbol": "[\"Ndc80\"]", "do": null }, { "gene_id": 67054, "description": "phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoribosylaminoimidazole, succinocarboxamide synthetase", "gene_symbol": "[\"Paics\"]", "do": null }, { "gene_id": 67063, "description": "post-GPI attachment to proteins GalNAc transferase 4", "gene_symbol": "[\"Pgap4\"]", "do": null }, { "gene_id": 67070, "description": "LSM14A mRNA processing body assembly factor", "gene_symbol": "[\"Lsm14a\"]", "do": null }, { "gene_id": 67072, "description": "cell division cycle 37-like 1", "gene_symbol": "[\"Cdc37l1\"]", "do": null }, { "gene_id": 67075, "description": "magnesium transporter 1", "gene_symbol": "[\"Magt1\"]", "do": "[{\"label\":\"primary immunodeficiency disease\",\"id\":\"DOID:612\"}]" }, { "gene_id": 67078, "description": "phosphoglycolate phosphatase", "gene_symbol": "[\"Pgp\"]", "do": null }, { "gene_id": 67095, "description": "trafficking protein, kinesin binding 1", "gene_symbol": "[\"Trak1\"]", "do": "[{\"label\":\"Stiff-Person syndrome\",\"id\":\"DOID:13366\"}]" }, { "gene_id": 67101, "description": "peroxisomal biogenesis factor 39", "gene_symbol": "[\"Pex39\"]", "do": null }, { "gene_id": 67111, "description": "N-acylethanolamine acid amidase", "gene_symbol": "[\"Naaa\"]", "do": null }, { "gene_id": 67118, "description": "bifunctional apoptosis regulator", "gene_symbol": "[\"Bfar\"]", "do": null }, { "gene_id": 67125, "description": "tetraspanin 31", "gene_symbol": "[\"Tspan31\"]", "do": null }, { "gene_id": 67133, "description": "glycoprotein 2 zymogen granule membrane", "gene_symbol": "[\"Gp2\"]", "do": null }, { "gene_id": 67134, "description": "NOP56 ribonucleoprotein", "gene_symbol": "[\"Nop56\"]", "do": null }, { "gene_id": 67141, "description": "F-box protein 5", "gene_symbol": "[\"Fbxo5\"]", "do": null }, { "gene_id": 67143, "description": "IKAROS family zinc finger 5", "gene_symbol": "[\"Ikzf5\"]", "do": null }, { "gene_id": 67144, "description": "leucine rich repeat containing 40", "gene_symbol": "[\"Lrrc40\"]", "do": null }, { "gene_id": 67149, "description": "Na+/K+ transporting ATPase interacting 1", "gene_symbol": "[\"Nkain1\"]", "do": null }, { "gene_id": 67151, "description": "proteasome (prosome, macropain) 26S subunit, non-ATPase, 9", "gene_symbol": "[\"Psmd9\"]", "do": null }, { "gene_id": 67154, "description": "metadherin", "gene_symbol": "[\"Mtdh\"]", "do": null }, { "gene_id": 67160, "description": "eukaryotic translation elongation factor 1 gamma", "gene_symbol": "[\"Eef1g\"]", "do": null }, { "gene_id": 67163, "description": "coiled-coil domain containing 47", "gene_symbol": "[\"Ccdc47\"]", "do": null }, { "gene_id": 67166, "description": "ADP-ribosylation factor-like 8B", "gene_symbol": "[\"Arl8b\"]", "do": null }, { "gene_id": 67168, "description": "lysophosphatidic acid receptor 6", "gene_symbol": "[\"Lpar6\"]", "do": null }, { "gene_id": 67169, "description": "neurotrophin receptor associated death domain", "gene_symbol": "[\"Nradd\"]", "do": null }, { "gene_id": 67186, "description": "ribosomal protein lateral stalk subunit P2", "gene_symbol": "[\"Rplp2\"]", "do": null }, { "gene_id": 67198, "description": "spermatogenesis associated, serine-rich 2-like", "gene_symbol": "[\"Spats2l\"]", "do": null }, { "gene_id": 67242, "description": "gem nuclear organelle associated protein 6", "gene_symbol": "[\"Gemin6\"]", "do": null }, { "gene_id": 67246, "description": "retroelement silencing factor 1", "gene_symbol": "[\"Resf1\"]", "do": null }, { "gene_id": 67252, "description": "cyclase associated actin cytoskeleton regulatory protein 2", "gene_symbol": "[\"Cap2\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 67260, "description": "ceramide synthase 4", "gene_symbol": "[\"Cers4\"]", "do": null }, { "gene_id": 67264, "description": "NADH:ubiquinone oxidoreductase subunit B8", "gene_symbol": "[\"Ndufb8\"]", "do": null }, { "gene_id": 67266, "description": "divergent protein kinase domain 1A", "gene_symbol": "[\"Dipk1a\"]", "do": null }, { "gene_id": 67287, "description": "poly (ADP-ribose) polymerase family, member 6", "gene_symbol": "[\"Parp6\"]", "do": null }, { "gene_id": 67300, "description": "clathrin heavy chain", "gene_symbol": "[\"Cltc\"]", "do": null }, { "gene_id": 67302, "description": "zinc finger CCCH type containing 13", "gene_symbol": "[\"Zc3h13\"]", "do": null }, { "gene_id": 67306, "description": "zinc finger, C2HC-type containing 1A", "gene_symbol": "[\"Zc2hc1a\"]", "do": null }, { "gene_id": 67310, "description": "prolactin family8, subfamily a, member 9", "gene_symbol": "[\"Prl8a9\"]", "do": null }, { "gene_id": 67311, "description": "N-acetylneuraminic acid phosphatase", "gene_symbol": "[\"Nanp\"]", "do": null }, { "gene_id": 67315, "description": "CEA cell adhesion molecule 12", "gene_symbol": "[\"Ceacam12\"]", "do": null }, { "gene_id": 67328, "description": "lysozyme-like 1", "gene_symbol": "[\"Lyzl1\"]", "do": null }, { "gene_id": 67332, "description": "small nuclear ribonucleoprotein D3", "gene_symbol": "[\"Snrpd3\"]", "do": null }, { "gene_id": 67366, "description": "transmembrane p24 trafficking protein 11", "gene_symbol": "[\"Tmed11\"]", "do": null }, { "gene_id": 67374, "description": "junction adhesion molecule 2", "gene_symbol": "[\"Jam2\"]", "do": null }, { "gene_id": 67375, "description": "quinolinate phosphoribosyltransferase", "gene_symbol": "[\"Qprt\"]", "do": null }, { "gene_id": 67382, "description": "bromodomain containing 3", "gene_symbol": "[\"Brd3\"]", "do": null }, { "gene_id": 67389, "description": "C1q and tumor necrosis factor related 12", "gene_symbol": "[\"C1qtnf12\"]", "do": null }, { "gene_id": 67391, "description": "FUN14 domain containing 2", "gene_symbol": "[\"Fundc2\"]", "do": null }, { "gene_id": 67393, "description": "CXXC finger 5", "gene_symbol": "[\"Cxxc5\"]", "do": null }, { "gene_id": 67399, "description": "PDZ and LIM domain 7", "gene_symbol": "[\"Pdlim7\"]", "do": null }, { "gene_id": 67416, "description": "armadillo repeat containing, X-linked 2", "gene_symbol": "[\"Armcx2\"]", "do": null }, { "gene_id": 67419, "description": "armadillo-like helical domain containing 4", "gene_symbol": "[\"Armh4\"]", "do": null }, { "gene_id": 67429, "description": "NudC domain containing 1", "gene_symbol": "[\"Nudcd1\"]", "do": null }, { "gene_id": 67448, "description": "plexin domain containing 2", "gene_symbol": "[\"Plxdc2\"]", "do": null }, { "gene_id": 67451, "description": "plakophilin 2", "gene_symbol": "[\"Pkp2\"]", "do": null }, { "gene_id": 67452, "description": "patatin-like phospholipase domain containing 8", "gene_symbol": "[\"Pnpla8\"]", "do": null }, { "gene_id": 67454, "description": "IKBKB interacting protein", "gene_symbol": "[\"Ikbip\"]", "do": null }, { "gene_id": 67456, "description": "ERGIC and golgi 2", "gene_symbol": "[\"Ergic2\"]", "do": null }, { "gene_id": 67458, "description": "endoplasmic reticulum-golgi intermediate compartment 1", "gene_symbol": "[\"Ergic1\"]", "do": null }, { "gene_id": 67464, "description": "ectonucleoside triphosphate diphosphohydrolase 4", "gene_symbol": "[\"Entpd4\"]", "do": null }, { "gene_id": 67465, "description": "splicing factor 3a, subunit 1", "gene_symbol": "[\"Sf3a1\"]", "do": null }, { "gene_id": 67470, "description": "ATP binding cassette subfamily G member 8", "gene_symbol": "[\"Abcg8\"]", "do": "[{\"label\":\"sitosterolemia\",\"id\":\"DOID:0090019\"}]" }, { "gene_id": 67474, "description": "synaptosomal-associated protein 29", "gene_symbol": "[\"Snap29\"]", "do": "[{\"label\":\"CEDNIK syndrome\",\"id\":\"DOID:0060337\"}]" }, { "gene_id": 67475, "description": "endoplasmic reticulum oxidoreductase 1 beta", "gene_symbol": "[\"Ero1b\"]", "do": null }, { "gene_id": 67490, "description": "UFM1 specific ligase 1", "gene_symbol": "[\"Ufl1\"]", "do": null }, { "gene_id": 67500, "description": "cell division cycle and apoptosis regulator 1", "gene_symbol": "[\"Ccar1\"]", "do": null }, { "gene_id": 67505, "description": "prolactin family 7, subfamily c, member 1", "gene_symbol": "[\"Prl7c1\"]", "do": null }, { "gene_id": 67511, "description": "transmembrane p24 trafficking protein 9", "gene_symbol": "[\"Tmed9\"]", "do": null }, { "gene_id": 67526, "description": "autophagy related 12", "gene_symbol": "[\"Atg12\"]", "do": null }, { "gene_id": 67533, "description": "PTPRF interacting protein, binding protein 1 (liprin beta 1)", "gene_symbol": "[\"Ppfibp1\"]", "do": null }, { "gene_id": 67537, "description": "GLI pathogenesis-related 1 like 2", "gene_symbol": "[\"Glipr1l2\"]", "do": null }, { "gene_id": 67542, "description": "component of oligomeric golgi complex 6", "gene_symbol": "[\"Cog6\"]", "do": null }, { "gene_id": 67547, "description": "solute carrier family 39 (metal ion transporter), member 8", "gene_symbol": "[\"Slc39a8\"]", "do": "[{\"label\":\"left ventricular noncompaction\",\"id\":\"DOID:0060480\"}]" }, { "gene_id": 67549, "description": "golgi pH regulator", "gene_symbol": "[\"Gphr\"]", "do": null }, { "gene_id": 67553, "description": "glutathione S-transferase, C-terminal domain containing", "gene_symbol": "[\"Gstcd\"]", "do": null }, { "gene_id": 67555, "description": "MGAT4 family, member D", "gene_symbol": "[\"Mgat4d\"]", "do": null }, { "gene_id": 67556, "description": "phosphatidylinositol glycan anchor biosynthesis, class M", "gene_symbol": "[\"Pigm\"]", "do": null }, { "gene_id": 67561, "description": "WD repeat domain 48", "gene_symbol": "[\"Wdr48\"]", "do": null }, { "gene_id": 67569, "description": "MGAT4 family, member C", "gene_symbol": "[\"Mgat4c\"]", "do": null }, { "gene_id": 67573, "description": "lysyl oxidase-like 4", "gene_symbol": "[\"Loxl4\"]", "do": null }, { "gene_id": 67574, "description": "asparagine-linked glycosylation 13", "gene_symbol": "[\"Alg13\"]", "do": null }, { "gene_id": 67590, "description": "tectonic family member 3", "gene_symbol": "[\"Tctn3\"]", "do": null }, { "gene_id": 67602, "description": "NECAP endocytosis associated 1", "gene_symbol": "[\"Necap1\"]", "do": null }, { "gene_id": 67605, "description": "AKT1 substrate 1", "gene_symbol": "[\"Akt1s1\"]", "do": null }, { "gene_id": 67606, "description": "fin bud initiation factor homolog (zebrafish)", "gene_symbol": "[\"Fibin\"]", "do": null }, { "gene_id": 67608, "description": "nuclear prelamin A recognition factor", "gene_symbol": "[\"Narf\"]", "do": null }, { "gene_id": 67610, "description": "ring finger and SPRY domain containing 1", "gene_symbol": "[\"Rspry1\"]", "do": null }, { "gene_id": 67615, "description": "ubiquitin-conjugating enzyme E2R 2", "gene_symbol": "[\"Ube2r2\"]", "do": null }, { "gene_id": 67623, "description": "transmembrane 7 superfamily member 3", "gene_symbol": "[\"Tm7sf3\"]", "do": null }, { "gene_id": 67646, "description": "RIKEN cDNA 4930522H14 gene", "gene_symbol": "[\"4930522H14Rik\"]", "do": null }, { "gene_id": 67647, "description": "RIKEN cDNA 4930523C07 gene", "gene_symbol": "[\"4930523C07Rik\"]", "do": null }, { "gene_id": 67652, "description": "sperm acrosome associated 1", "gene_symbol": "[\"Spaca1\"]", "do": null }, { "gene_id": 67665, "description": "dynactin 4", "gene_symbol": "[\"Dctn4\"]", "do": null }, { "gene_id": 67698, "description": "family with sequence similarity 174, member A", "gene_symbol": "[\"Fam174a\"]", "do": null }, { "gene_id": 67702, "description": "ring finger protein 149", "gene_symbol": "[\"Rnf149\"]", "do": null }, { "gene_id": 67703, "description": "kirre like nephrin family adhesion molecule 3", "gene_symbol": "[\"Kirrel3\"]", "do": null }, { "gene_id": 67708, "description": "pecanex homolog 4", "gene_symbol": "[\"Pcnx4\"]", "do": null }, { "gene_id": 67709, "description": "regenerating islet-derived family, member 4", "gene_symbol": "[\"Reg4\"]", "do": null }, { "gene_id": 67717, "description": "lipase F, gastric type", "gene_symbol": "[\"Lipf\"]", "do": null }, { "gene_id": 67719, "description": "RIKEN cDNA 2310057J18 gene", "gene_symbol": "[\"2310057J18Rik\"]", "do": null }, { "gene_id": 67726, "description": "family with sequence similarity 114, member A2", "gene_symbol": "[\"Fam114a2\"]", "do": null }, { "gene_id": 67728, "description": "DPH2 homolog", "gene_symbol": "[\"Dph2\"]", "do": null }, { "gene_id": 67729, "description": "MANSC domain containing 1", "gene_symbol": "[\"Mansc1\"]", "do": null }, { "gene_id": 67732, "description": "isoamyl acetate-hydrolyzing esterase 1 homolog", "gene_symbol": "[\"Iah1\"]", "do": null }, { "gene_id": 67753, "description": "equatorin, sperm acrosome associated", "gene_symbol": "[\"Eqtn\"]", "do": null }, { "gene_id": 67758, "description": "arylacetamide deacetylase", "gene_symbol": "[\"Aadac\"]", "do": null }, { "gene_id": 67760, "description": "solute carrier family 38, member 2", "gene_symbol": "[\"Slc38a2\"]", "do": null }, { "gene_id": 67763, "description": "phosphoribosyl pyrophosphate synthetase-associated protein 1", "gene_symbol": "[\"Prpsap1\"]", "do": null }, { "gene_id": 67772, "description": "chromodomain helicase DNA binding protein 8", "gene_symbol": "[\"Chd8\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 67776, "description": "von Willebrand factor A domain containing 5A", "gene_symbol": "[\"Vwa5a\"]", "do": null }, { "gene_id": 67784, "description": "plexin D1", "gene_symbol": "[\"Plxnd1\"]", "do": "[{\"label\":\"DiGeorge syndrome\",\"id\":\"DOID:11198\"}]" }, { "gene_id": 67800, "description": "diacylglycerol O-acyltransferase 2", "gene_symbol": "[\"Dgat2\"]", "do": null }, { "gene_id": 67804, "description": "sorting nexin 2", "gene_symbol": "[\"Snx2\"]", "do": null }, { "gene_id": 67812, "description": "UBX domain protein 4", "gene_symbol": "[\"Ubxn4\"]", "do": null }, { "gene_id": 67826, "description": "synaptosomal-associated protein, 47", "gene_symbol": "[\"Snap47\"]", "do": null }, { "gene_id": 67834, "description": "isocitrate dehydrogenase 3 (NAD+) alpha", "gene_symbol": "[\"Idh3a\"]", "do": null }, { "gene_id": 67838, "description": "DnaJ heat shock protein family (Hsp40) member B11", "gene_symbol": "[\"Dnajb11\"]", "do": null }, { "gene_id": 67839, "description": "G-protein signalling modulator 1 (AGS3-like, C. elegans)", "gene_symbol": "[\"Gpsm1\"]", "do": null }, { "gene_id": 67841, "description": "autophagy related 3", "gene_symbol": "[\"Atg3\"]", "do": null }, { "gene_id": 67846, "description": "transmembrane protein 39a", "gene_symbol": "[\"Tmem39a\"]", "do": null }, { "gene_id": 67847, "description": "synuclein, alpha interacting protein (synphilin)", "gene_symbol": "[\"Sncaip\"]", "do": null }, { "gene_id": 67848, "description": "DEAD box helicase 55", "gene_symbol": "[\"Ddx55\"]", "do": null }, { "gene_id": 67855, "description": "aspartic peptidase, retroviral-like 1", "gene_symbol": "[\"Asprv1\"]", "do": null }, { "gene_id": 67856, "description": "enoyl Coenzyme A hydratase domain containing 3", "gene_symbol": "[\"Echdc3\"]", "do": null }, { "gene_id": 67857, "description": "protein phosphatase 6, catalytic subunit", "gene_symbol": "[\"Ppp6c\"]", "do": null }, { "gene_id": 67863, "description": "solute carrier family 25 (mitochondrial carrier oxoglutarate carrier), member 11", "gene_symbol": "[\"Slc25a11\"]", "do": null }, { "gene_id": 67874, "description": "reprimo, TP53 dependent G2 arrest mediator candidate", "gene_symbol": "[\"Rprm\"]", "do": null }, { "gene_id": 67880, "description": "dicarbonyl L-xylulose reductase", "gene_symbol": "[\"Dcxr\"]", "do": null }, { "gene_id": 67883, "description": "UDP-glucuronate decarboxylase 1", "gene_symbol": "[\"Uxs1\"]", "do": null }, { "gene_id": 67891, "description": "ribosomal protein L4", "gene_symbol": "[\"Rpl4\"]", "do": null }, { "gene_id": 67896, "description": "coiled-coil domain containing 80", "gene_symbol": "[\"Ccdc80\"]", "do": null }, { "gene_id": 67897, "description": "RNA (guanine-7-) methyltransferase", "gene_symbol": "[\"Rnmt\"]", "do": null }, { "gene_id": 67898, "description": "penta-EF hand domain containing 1", "gene_symbol": "[\"Pef1\"]", "do": null }, { "gene_id": 67902, "description": "sulfatase modifying factor 2", "gene_symbol": "[\"Sumf2\"]", "do": null }, { "gene_id": 67909, "description": "UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5", "gene_symbol": "[\"Galntl5\"]", "do": null }, { "gene_id": 67912, "description": "RIKEN cDNA 1600012H06 gene", "gene_symbol": "[\"1600012H06Rik\"]", "do": null }, { "gene_id": 67914, "description": "coenzyme Q9", "gene_symbol": "[\"Coq9\"]", "do": "[{\"label\":\"coenzyme Q10 deficiency disease\",\"id\":\"DOID:0050730\"}]" }, { "gene_id": 67916, "description": "phospholipid phosphatase 3", "gene_symbol": "[\"Plpp3\"]", "do": null }, { "gene_id": 67931, "description": "serine (or cysteine) peptidase inhibitor, clade I, member 2", "gene_symbol": "[\"Serpini2\"]", "do": "[{\"label\":\"Shwachman-Diamond syndrome\",\"id\":\"DOID:0060479\"}]" }, { "gene_id": 67933, "description": "host cell factor C2", "gene_symbol": "[\"Hcfc2\"]", "do": null }, { "gene_id": 67935, "description": "carboxylesterase 5A", "gene_symbol": "[\"Ces5a\"]", "do": null }, { "gene_id": 67937, "description": "transmembrane protein 59-like", "gene_symbol": "[\"Tmem59l\"]", "do": null }, { "gene_id": 67943, "description": "mesoderm development LRP chaperone", "gene_symbol": "[\"Mesd\"]", "do": null }, { "gene_id": 67949, "description": "nucleolar protein interacting with the FHA domain of MKI67", "gene_symbol": "[\"Nifk\"]", "do": null }, { "gene_id": 67951, "description": "tubulin, beta 6 class V", "gene_symbol": "[\"Tubb6\"]", "do": null }, { "gene_id": 67958, "description": "U2 snRNP-associated SURP domain containing", "gene_symbol": "[\"U2surp\"]", "do": null }, { "gene_id": 67959, "description": "poly-U binding splicing factor 60", "gene_symbol": "[\"Puf60\"]", "do": null }, { "gene_id": 67963, "description": "NPC intracellular cholesterol transporter 2", "gene_symbol": "[\"Npc2\"]", "do": "[{\"label\":\"Niemann-Pick disease\",\"id\":\"DOID:14504\"}]" }, { "gene_id": 67971, "description": "tubulin polymerization-promoting protein family member 3", "gene_symbol": "[\"Tppp3\"]", "do": null }, { "gene_id": 67972, "description": "ATPase, Ca++ transporting, plasma membrane 1", "gene_symbol": "[\"Atp2b1\"]", "do": null }, { "gene_id": 67978, "description": "tectonic family member 2", "gene_symbol": "[\"Tctn2\"]", "do": null }, { "gene_id": 67979, "description": "ATPase family, AAA domain containing 1", "gene_symbol": "[\"Atad1\"]", "do": null }, { "gene_id": 67980, "description": "glucosamine-6-phosphate deaminase 2", "gene_symbol": "[\"Gnpda2\"]", "do": null }, { "gene_id": 67988, "description": "thioredoxin-related transmembrane protein 3", "gene_symbol": "[\"Tmx3\"]", "do": null }, { "gene_id": 67996, "description": "serine and arginine-rich splicing factor 6", "gene_symbol": "[\"Srsf6\"]", "do": null }, { "gene_id": 68010, "description": "BMP and activin membrane-bound inhibitor", "gene_symbol": "[\"Bambi\"]", "do": null }, { "gene_id": 68015, "description": "TNF receptor-associated protein 1", "gene_symbol": "[\"Trap1\"]", "do": null }, { "gene_id": 68016, "description": "caveolae associated 4", "gene_symbol": "[\"Cavin4\"]", "do": null }, { "gene_id": 68024, "description": "H2B clustered histone 4", "gene_symbol": "[\"H2bc4\"]", "do": null }, { "gene_id": 68027, "description": "transmembrane protein 178", "gene_symbol": "[\"Tmem178\"]", "do": null }, { "gene_id": 68031, "description": "ring finger protein 146", "gene_symbol": "[\"Rnf146\"]", "do": "[{\"label\":\"osteochondrodysplasia\",\"id\":\"DOID:2256\"}]" }, { "gene_id": 68038, "description": "chitinase domain containing 1", "gene_symbol": "[\"Chid1\"]", "do": null }, { "gene_id": 68054, "description": "serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12", "gene_symbol": "[\"Serpina12\"]", "do": null }, { "gene_id": 68070, "description": "PDZ domain containing 2", "gene_symbol": "[\"Pdzd2\"]", "do": null }, { "gene_id": 68094, "description": "SWI/SNF related BAF chromatin remodeling complex subunit C2", "gene_symbol": "[\"Smarcc2\"]", "do": null }, { "gene_id": 68095, "description": "OCIA domain containing 1", "gene_symbol": "[\"Ociad1\"]", "do": null }, { "gene_id": 68117, "description": "apolipoprotein O-like", "gene_symbol": "[\"Apool\"]", "do": null }, { "gene_id": 68146, "description": "ADP-ribosylation factor-like 13B", "gene_symbol": "[\"Arl13b\"]", "do": null }, { "gene_id": 68152, "description": "family with sequence similarity 133, member B", "gene_symbol": "[\"Fam133b\"]", "do": null }, { "gene_id": 68169, "description": "neuron-derived neurotrophic factor", "gene_symbol": "[\"Ndnf\"]", "do": null }, { "gene_id": 68183, "description": "BCAS2 pre-mRNA processing factor", "gene_symbol": "[\"Bcas2\"]", "do": null }, { "gene_id": 68187, "description": "family with sequence similarity 135, member A", "gene_symbol": "[\"Fam135a\"]", "do": null }, { "gene_id": 68195, "description": "ribonuclease T2B", "gene_symbol": "[\"Rnaset2b\"]", "do": null }, { "gene_id": 68214, "description": "glutathione S-transferase omega 2", "gene_symbol": "[\"Gsto2\"]", "do": null }, { "gene_id": 68251, "description": "BRISC and BRCA1 A complex member 1", "gene_symbol": "[\"Babam1\"]", "do": null }, { "gene_id": 68263, "description": "pyruvate dehydrogenase (lipoamide) beta", "gene_symbol": "[\"Pdhb\"]", "do": null }, { "gene_id": 68267, "description": "solute carrier family 25 (mitochondrial carrier, glutamate), member 22", "gene_symbol": "[\"Slc25a22\"]", "do": null }, { "gene_id": 68273, "description": "protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase", "gene_symbol": "[\"Pomgnt1\"]", "do": "[{\"label\":\"Walker-Warburg syndrome\",\"id\":\"DOID:0050560\"},{\"label\":\"muscular dystrophy-dystroglycanopathy type B1\",\"id\":\"DOID:0050588\"}]" }, { "gene_id": 68275, "description": "replication protein A1", "gene_symbol": "[\"Rpa1\"]", "do": null }, { "gene_id": 68276, "description": "target of EGR1, member 1 (nuclear)", "gene_symbol": "[\"Toe1\"]", "do": null }, { "gene_id": 68291, "description": "mitochondrial tRNA translation optimization 1", "gene_symbol": "[\"Mto1\"]", "do": "[{\"label\":\"combined oxidative phosphorylation deficiency\",\"id\":\"DOID:0060286\"}]" }, { "gene_id": 68292, "description": "STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)", "gene_symbol": "[\"Stt3b\"]", "do": null }, { "gene_id": 68294, "description": "solute carrier family 75 member 1", "gene_symbol": "[\"Slc75a1\"]", "do": null }, { "gene_id": 68303, "description": "family with sequence similarity 114, member A1", "gene_symbol": "[\"Fam114a1\"]", "do": null }, { "gene_id": 68304, "description": "protein O-glucosyltransferase 3", "gene_symbol": "[\"Poglut3\"]", "do": null }, { "gene_id": 68311, "description": "Ly6/Plaur domain containing 2", "gene_symbol": "[\"Lypd2\"]", "do": null }, { "gene_id": 68316, "description": "apolipoprotein O", "gene_symbol": "[\"Apoo\"]", "do": null }, { "gene_id": 68337, "description": "cysteine rich protein 2", "gene_symbol": "[\"Crip2\"]", "do": null }, { "gene_id": 68342, "description": "NADH:ubiquinone oxidoreductase subunit B10", "gene_symbol": "[\"Ndufb10\"]", "do": null }, { "gene_id": 68348, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 1F", "gene_symbol": "[\"Serpina1f\"]", "do": null }, { "gene_id": 68365, "description": "RAB14, member RAS oncogene family", "gene_symbol": "[\"Rab14\"]", "do": null }, { "gene_id": 68393, "description": "monoacylglycerol O-acyltransferase 1", "gene_symbol": "[\"Mogat1\"]", "do": null }, { "gene_id": 68395, "description": "histocompatibility 2, Q region locus 8", "gene_symbol": "[\"H2-Q8\"]", "do": null }, { "gene_id": 68401, "description": "glucose 6 phosphatase, catalytic, 3", "gene_symbol": "[\"G6pc3\"]", "do": null }, { "gene_id": 68421, "description": "LMBR1 domain containing 1", "gene_symbol": "[\"Lmbrd1\"]", "do": null }, { "gene_id": 68428, "description": "STEAP family member 3", "gene_symbol": "[\"Steap3\"]", "do": null }, { "gene_id": 68449, "description": "TBC1 domain family, member 10b", "gene_symbol": "[\"Tbc1d10b\"]", "do": null }, { "gene_id": 68453, "description": "GPI-anchored HDL-binding protein 1", "gene_symbol": "[\"Gpihbp1\"]", "do": null }, { "gene_id": 68468, "description": "lymphocyte antigen 6 family member G6C", "gene_symbol": "[\"Ly6g6c\"]", "do": null }, { "gene_id": 68481, "description": "myelin protein zero-like 1", "gene_symbol": "[\"Mpzl1\"]", "do": null }, { "gene_id": 68498, "description": "tetraspanin 11", "gene_symbol": "[\"Tspan11\"]", "do": null }, { "gene_id": 68505, "description": "VPS51 GARP complex subunit", "gene_symbol": "[\"Vps51\"]", "do": null }, { "gene_id": 68510, "description": "integrator complex subunit 1", "gene_symbol": "[\"Ints1\"]", "do": null }, { "gene_id": 68519, "description": "echinoderm microtubule associated protein like 1", "gene_symbol": "[\"Eml1\"]", "do": "[{\"label\":\"congenital nervous system abnormality\",\"id\":\"DOID:2490\"},{\"label\":\"subcortical band heterotopia\",\"id\":\"DOID:0111169\"}]" }, { "gene_id": 68521, "description": "endosomal transmembrane epsin interactor 3", "gene_symbol": "[\"Entrep3\"]", "do": null }, { "gene_id": 68524, "description": "WAS/WASL interacting protein family, member 2", "gene_symbol": "[\"Wipf2\"]", "do": null }, { "gene_id": 68525, "description": "EvC ciliary complex subunit 2", "gene_symbol": "[\"Evc2\"]", "do": "[{\"label\":\"Ellis-Van Creveld syndrome\",\"id\":\"DOID:12714\"}]" }, { "gene_id": 68526, "description": "G protein-coupled receptor 155", "gene_symbol": "[\"Gpr155\"]", "do": null }, { "gene_id": 68544, "description": "telomerase RNA component interacting RNase", "gene_symbol": "[\"Trir\"]", "do": null }, { "gene_id": 68549, "description": "shugoshin 2A", "gene_symbol": "[\"Sgo2a\"]", "do": null }, { "gene_id": 68553, "description": "collagen, type VI, alpha 4", "gene_symbol": "[\"Col6a4\"]", "do": null }, { "gene_id": 68564, "description": "nuclear FMR1 interacting protein 2", "gene_symbol": "[\"Nufip2\"]", "do": null }, { "gene_id": 68581, "description": "transmembrane p24 trafficking protein 10", "gene_symbol": "[\"Tmed10\"]", "do": null }, { "gene_id": 68585, "description": "reticulon 4", "gene_symbol": "[\"Rtn4\"]", "do": null }, { "gene_id": 68588, "description": "collagen triple helix repeat containing 1", "gene_symbol": "[\"Cthrc1\"]", "do": null }, { "gene_id": 68617, "description": "microtubule crosslinking factor 1", "gene_symbol": "[\"Mtcl1\"]", "do": null }, { "gene_id": 68634, "description": "TM2 domain containing 3", "gene_symbol": "[\"Tm2d3\"]", "do": null }, { "gene_id": 68644, "description": "abhydrolase domain containing 14A", "gene_symbol": "[\"Abhd14a\"]", "do": null }, { "gene_id": 68646, "description": "NAD kinase 2, mitochondrial", "gene_symbol": "[\"Nadk2\"]", "do": null }, { "gene_id": 68652, "description": "TGF-beta activated kinase 1/MAP3K7 binding protein 2", "gene_symbol": "[\"Tab2\"]", "do": null }, { "gene_id": 68659, "description": "golgi associated kinase 1B", "gene_symbol": "[\"Gask1b\"]", "do": null }, { "gene_id": 68667, "description": "transient receptor potential cation channel, subfamily M, member 4", "gene_symbol": "[\"Trpm4\"]", "do": null }, { "gene_id": 68668, "description": "kallikrein related-peptidase 5", "gene_symbol": "[\"Klk5\"]", "do": null }, { "gene_id": 68675, "description": "ARB2 cotranscriptional regulator A", "gene_symbol": "[\"Arb2a\"]", "do": null }, { "gene_id": 68682, "description": "solute carrier family 44, member 2", "gene_symbol": "[\"Slc44a2\"]", "do": null }, { "gene_id": 68703, "description": "arginine glutamic acid dipeptide (RE) repeats", "gene_symbol": "[\"Rere\"]", "do": null }, { "gene_id": 68705, "description": "general transcription factor IIF, polypeptide 2", "gene_symbol": "[\"Gtf2f2\"]", "do": null }, { "gene_id": 68709, "description": "cartilage intermediate layer protein 2", "gene_symbol": "[\"Cilp2\"]", "do": null }, { "gene_id": 68729, "description": "tripartite motif-containing 37", "gene_symbol": "[\"Trim37\"]", "do": "[{\"label\":\"mulibrey nanism\",\"id\":\"DOID:0050436\"}]" }, { "gene_id": 68734, "description": "protein phosphatase 4 regulatory subunit 3A", "gene_symbol": "[\"Ppp4r3a\"]", "do": null }, { "gene_id": 68742, "description": "transmembrane protein 219", "gene_symbol": "[\"Tmem219\"]", "do": null }, { "gene_id": 68743, "description": "anillin, actin binding protein", "gene_symbol": "[\"Anln\"]", "do": null }, { "gene_id": 68750, "description": "ras responsive element binding protein 1", "gene_symbol": "[\"Rreb1\"]", "do": "[{\"label\":\"RASopathy\",\"id\":\"DOID:0080690\"}]" }, { "gene_id": 68760, "description": "synaptopodin 2-like", "gene_symbol": "[\"Synpo2l\"]", "do": null }, { "gene_id": 68764, "description": "cadherin-related family member 3", "gene_symbol": "[\"Cdhr3\"]", "do": null }, { "gene_id": 68770, "description": "putative homeodomain transcription factor 2", "gene_symbol": "[\"Phtf2\"]", "do": null }, { "gene_id": 68794, "description": "filamin C, gamma", "gene_symbol": "[\"Flnc\"]", "do": "[{\"label\":\"myofibrillar myopathy 5\",\"id\":\"DOID:0080096\"}]" }, { "gene_id": 68796, "description": "transmembrane protein 214", "gene_symbol": "[\"Tmem214\"]", "do": null }, { "gene_id": 68797, "description": "platelet-derived growth factor receptor-like", "gene_symbol": "[\"Pdgfrl\"]", "do": null }, { "gene_id": 68799, "description": "repulsive guidance molecule family member B", "gene_symbol": "[\"Rgmb\"]", "do": null }, { "gene_id": 68802, "description": "myopalladin", "gene_symbol": "[\"Mypn\"]", "do": "[{\"label\":\"nemaline myopathy 11\",\"id\":\"DOID:0110933\"},{\"label\":\"restrictive cardiomyopathy\",\"id\":\"DOID:397\"}]" }, { "gene_id": 68818, "description": "zinc finger, AN1 type domain 2B", "gene_symbol": "[\"Zfand2b\"]", "do": null }, { "gene_id": 68828, "description": "syncoilin", "gene_symbol": "[\"Sync\"]", "do": null }, { "gene_id": 68837, "description": "forkhead box K2", "gene_symbol": "[\"Foxk2\"]", "do": null }, { "gene_id": 68842, "description": "TUB like protein 4", "gene_symbol": "[\"Tulp4\"]", "do": null }, { "gene_id": 68852, "description": "LRRN4 C-terminal like", "gene_symbol": "[\"Lrrn4cl\"]", "do": null }, { "gene_id": 68875, "description": "transmembrane and coiled-coil domains 2", "gene_symbol": "[\"Tmcc2\"]", "do": null }, { "gene_id": 68888, "description": "gastrokine 3", "gene_symbol": "[\"Gkn3\"]", "do": null }, { "gene_id": 68889, "description": "ubiquitin associated domain containing 2", "gene_symbol": "[\"Ubac2\"]", "do": null }, { "gene_id": 68891, "description": "CD177 antigen", "gene_symbol": "[\"Cd177\"]", "do": null }, { "gene_id": 68897, "description": "dispatched RND transporter family member 1", "gene_symbol": "[\"Disp1\"]", "do": null }, { "gene_id": 68904, "description": "abhydrolase domain containing 13", "gene_symbol": "[\"Abhd13\"]", "do": null }, { "gene_id": 68916, "description": "CDK5 regulatory subunit associated protein 1-like 1", "gene_symbol": "[\"Cdkal1\"]", "do": "[{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 68922, "description": "dynein axonemal intermediate chain 1", "gene_symbol": "[\"Dnai1\"]", "do": "[{\"label\":\"Kartagener syndrome\",\"id\":\"DOID:0050144\"},{\"label\":\"primary ciliary dyskinesia 1\",\"id\":\"DOID:0110594\"},{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 68926, "description": "ubiquitin-associated protein 2", "gene_symbol": "[\"Ubap2\"]", "do": null }, { "gene_id": 68943, "description": "PTEN induced putative kinase 1", "gene_symbol": "[\"Pink1\"]", "do": null }, { "gene_id": 68947, "description": "carbohydrate sulfotransferase 8", "gene_symbol": "[\"Chst8\"]", "do": null }, { "gene_id": 68961, "description": "phosphorylase kinase, gamma 2 (testis)", "gene_symbol": "[\"Phkg2\"]", "do": null }, { "gene_id": 68968, "description": "codanin 1", "gene_symbol": "[\"Cdan1\"]", "do": null }, { "gene_id": 68981, "description": "small nuclear ribonucleoprotein polypeptide A'", "gene_symbol": "[\"Snrpa1\"]", "do": null }, { "gene_id": 69017, "description": "proline-rich transmembrane protein 2", "gene_symbol": "[\"Prrt2\"]", "do": "[{\"label\":\"episodic kinesigenic dyskinesia 1\",\"id\":\"DOID:0090053\"}]" }, { "gene_id": 69024, "description": "sorting nexin 15", "gene_symbol": "[\"Snx15\"]", "do": null }, { "gene_id": 69032, "description": "lysozyme-like 4", "gene_symbol": "[\"Lyzl4\"]", "do": null }, { "gene_id": 69064, "description": "fucose mutarotase", "gene_symbol": "[\"Fuom\"]", "do": null }, { "gene_id": 69072, "description": "EBNA1 binding protein 2", "gene_symbol": "[\"Ebna1bp2\"]", "do": null }, { "gene_id": 69077, "description": "proteasome (prosome, macropain) 26S subunit, non-ATPase, 11", "gene_symbol": "[\"Psmd11\"]", "do": null }, { "gene_id": 69083, "description": "sulfotransferase family, cytosolic, 1C, member 2", "gene_symbol": "[\"Sult1c2\"]", "do": null }, { "gene_id": 69101, "description": "YdjC homolog (bacterial)", "gene_symbol": "[\"Ydjc\"]", "do": null }, { "gene_id": 69116, "description": "ubiquitin protein ligase E3 component n-recognin 4", "gene_symbol": "[\"Ubr4\"]", "do": null }, { "gene_id": 69121, "description": "chordin-like 2", "gene_symbol": "[\"Chrdl2\"]", "do": null }, { "gene_id": 69131, "description": "cyclin dependent kinase 12", "gene_symbol": "[\"Cdk12\"]", "do": null }, { "gene_id": 69137, "description": "V-set and transmembrane domain containing 5", "gene_symbol": "[\"Vstm5\"]", "do": null }, { "gene_id": 69151, "description": "leucine zipper and CTNNBIP1 domain containing", "gene_symbol": "[\"Lzic\"]", "do": null }, { "gene_id": 69162, "description": "SEC31 homolog A, COPII coat complex component", "gene_symbol": "[\"Sec31a\"]", "do": null }, { "gene_id": 69165, "description": "CD209b antigen", "gene_symbol": "[\"Cd209b\"]", "do": null }, { "gene_id": 69168, "description": "bolA family member 1", "gene_symbol": "[\"Bola1\"]", "do": null }, { "gene_id": 69179, "description": "STIM activating enhancer", "gene_symbol": "[\"Stimate\"]", "do": null }, { "gene_id": 69183, "description": "C1q and tumor necrosis factor related protein 2", "gene_symbol": "[\"C1qtnf2\"]", "do": null }, { "gene_id": 69187, "description": "endoplasmic reticulum protein 27", "gene_symbol": "[\"Erp27\"]", "do": null }, { "gene_id": 69188, "description": "lysine (K)-specific methyltransferase 2E", "gene_symbol": "[\"Kmt2e\"]", "do": null }, { "gene_id": 69189, "description": "mast cell expressed membrane protein 1", "gene_symbol": "[\"Mcemp1\"]", "do": null }, { "gene_id": 69191, "description": "protein disulfide isomerase associated 2", "gene_symbol": "[\"Pdia2\"]", "do": null }, { "gene_id": 69207, "description": "serine and arginine-rich splicing factor 11", "gene_symbol": "[\"Srsf11\"]", "do": null }, { "gene_id": 69219, "description": "dimethylarginine dimethylaminohydrolase 1", "gene_symbol": "[\"Ddah1\"]", "do": null }, { "gene_id": 69225, "description": "NAD(P)HX dehydratase", "gene_symbol": "[\"Naxd\"]", "do": null }, { "gene_id": 69232, "description": "glutamine-rich 1", "gene_symbol": "[\"Qrich1\"]", "do": null }, { "gene_id": 69257, "description": "E74-like factor 2", "gene_symbol": "[\"Elf2\"]", "do": null }, { "gene_id": 69269, "description": "sodium channel modifier 1", "gene_symbol": "[\"Scnm1\"]", "do": null }, { "gene_id": 69286, "description": "GLI pathogenesis-related 1 like 1", "gene_symbol": "[\"Glipr1l1\"]", "do": null }, { "gene_id": 69296, "description": "transmembrane and immunoglobulin domain containing 3", "gene_symbol": "[\"Tmigd3\"]", "do": null }, { "gene_id": 69312, "description": "protein phosphatase 1, regulatory subunit 42", "gene_symbol": "[\"Ppp1r42\"]", "do": null }, { "gene_id": 69314, "description": "IZUMO family member 3", "gene_symbol": "[\"Izumo3\"]", "do": null }, { "gene_id": 69354, "description": "solute carrier family 38, member 4", "gene_symbol": "[\"Slc38a4\"]", "do": null }, { "gene_id": 69362, "description": "cystatin 12", "gene_symbol": "[\"Cst12\"]", "do": null }, { "gene_id": 69376, "description": "zona pellucida binding protein 2", "gene_symbol": "[\"Zpbp2\"]", "do": null }, { "gene_id": 69379, "description": "complement component 8, gamma polypeptide", "gene_symbol": "[\"C8g\"]", "do": null }, { "gene_id": 69386, "description": "H4 clustered histone 8", "gene_symbol": "[\"H4c8\"]", "do": null }, { "gene_id": 69444, "description": "lysozyme-like 6", "gene_symbol": "[\"Lyzl6\"]", "do": null }, { "gene_id": 69453, "description": "serine protease 56", "gene_symbol": "[\"Prss56\"]", "do": "[{\"label\":\"isolated microphthalmia 6\",\"id\":\"DOID:0060835\"}]" }, { "gene_id": 69482, "description": "nucleoporin 35", "gene_symbol": "[\"Nup35\"]", "do": "[{\"label\":\"intestinal pseudo-obstruction\",\"id\":\"DOID:0080072\"}]" }, { "gene_id": 69524, "description": "endothelial cell-specific adhesion molecule", "gene_symbol": "[\"Esam\"]", "do": null }, { "gene_id": 69537, "description": "deoxyribonuclease 1-like 1", "gene_symbol": "[\"Dnase1l1\"]", "do": null }, { "gene_id": 69538, "description": "anthrax toxin receptor 1", "gene_symbol": "[\"Antxr1\"]", "do": null }, { "gene_id": 69541, "description": "lysozyme G-like 1", "gene_symbol": "[\"Lyg1\"]", "do": null }, { "gene_id": 69550, "description": "bone marrow stromal cell antigen 2", "gene_symbol": "[\"Bst2\"]", "do": null }, { "gene_id": 69562, "description": "cyclin dependent kinase 13", "gene_symbol": "[\"Cdk13\"]", "do": "[{\"label\":\"congenital heart defects, dysmorphic facial features, and intellectual developmental disorder\",\"id\":\"DOID:0112247\"}]" }, { "gene_id": 69583, "description": "tumor necrosis factor (ligand) superfamily, member 13", "gene_symbol": "[\"Tnfsf13\"]", "do": null }, { "gene_id": 69585, "description": "hemojuvelin BMP co-receptor", "gene_symbol": "[\"Hjv\"]", "do": "[{\"label\":\"hemochromatosis type 2A\",\"id\":\"DOID:0111027\"}]" }, { "gene_id": 69592, "description": "odontogenic, ameloblast asssociated", "gene_symbol": "[\"Odam\"]", "do": null }, { "gene_id": 69597, "description": "AFG3-like AAA ATPase 2", "gene_symbol": "[\"Afg3l2\"]", "do": "[{\"label\":\"spinocerebellar ataxia 28\",\"id\":\"DOID:0050977\"}]" }, { "gene_id": 69601, "description": "disabled 2 interacting protein", "gene_symbol": "[\"Dab2ip\"]", "do": null }, { "gene_id": 69605, "description": "lunapark, ER junction formation factor", "gene_symbol": "[\"Lnpk\"]", "do": null }, { "gene_id": 69608, "description": "SEC24 homolog D, COPII coat complex component", "gene_symbol": "[\"Sec24d\"]", "do": null }, { "gene_id": 69617, "description": "pitrilysin metallepetidase 1", "gene_symbol": "[\"Pitrm1\"]", "do": null }, { "gene_id": 69632, "description": "Rho guanine nucleotide exchange factor 12", "gene_symbol": "[\"Arhgef12\"]", "do": null }, { "gene_id": 69634, "description": "citrate lyase beta like", "gene_symbol": "[\"Clybl\"]", "do": null }, { "gene_id": 69635, "description": "death associated protein kinase 1", "gene_symbol": "[\"Dapk1\"]", "do": null }, { "gene_id": 69642, "description": "muscular LMNA-interacting protein", "gene_symbol": "[\"Mlip\"]", "do": null }, { "gene_id": 69655, "description": "CD164 sialomucin-like 2", "gene_symbol": "[\"Cd164l2\"]", "do": null }, { "gene_id": 69665, "description": "uroplakin 3B-like", "gene_symbol": "[\"Upk3bl\"]", "do": null }, { "gene_id": 69672, "description": "thioredoxin domain containing 15", "gene_symbol": "[\"Txndc15\"]", "do": null }, { "gene_id": 69675, "description": "peroxidasin", "gene_symbol": "[\"Pxdn\"]", "do": null }, { "gene_id": 69683, "description": "ER membrane protein complex subunit 10", "gene_symbol": "[\"Emc10\"]", "do": null }, { "gene_id": 69697, "description": "calmodulin regulated spectrin-associated protein family, member 3", "gene_symbol": "[\"Camsap3\"]", "do": null }, { "gene_id": 69698, "description": "solute carrier protein family 52, member 3", "gene_symbol": "[\"Slc52a3\"]", "do": null }, { "gene_id": 69714, "description": "TCF3 (E2A) fusion partner", "gene_symbol": "[\"Tfpt\"]", "do": null }, { "gene_id": 69719, "description": "carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase", "gene_symbol": "[\"Cad\"]", "do": null }, { "gene_id": 69742, "description": "TM2 domain containing 2", "gene_symbol": "[\"Tm2d2\"]", "do": null }, { "gene_id": 69743, "description": "castor zinc finger 1", "gene_symbol": "[\"Casz1\"]", "do": "[{\"label\":\"chromosome 1p36 deletion syndrome\",\"id\":\"DOID:0060410\"}]" }, { "gene_id": 69770, "description": "family with sequence similarity 174, member C", "gene_symbol": "[\"Fam174c\"]", "do": null }, { "gene_id": 69780, "description": "small ArfGAP 2", "gene_symbol": "[\"Smap2\"]", "do": null }, { "gene_id": 69787, "description": "annexin A13", "gene_symbol": "[\"Anxa13\"]", "do": null }, { "gene_id": 69847, "description": "WNK lysine deficient protein kinase 4", "gene_symbol": "[\"Wnk4\"]", "do": "[{\"label\":\"Gitelman syndrome\",\"id\":\"DOID:0050450\"},{\"label\":\"pseudohypoaldosteronism\",\"id\":\"DOID:4479\"}]" }, { "gene_id": 69865, "description": "APOBEC1 complementation factor", "gene_symbol": "[\"A1cf\"]", "do": null }, { "gene_id": 69900, "description": "major facilitator superfamily domain containing 11", "gene_symbol": "[\"Mfsd11\"]", "do": null }, { "gene_id": 69940, "description": "exocyst complex component 1", "gene_symbol": "[\"Exoc1\"]", "do": null }, { "gene_id": 69944, "description": "RIKEN cDNA 2810021J22 gene", "gene_symbol": "[\"2810021J22Rik\"]", "do": null }, { "gene_id": 69961, "description": "ribonuclease P/MRP 25 subunit-like", "gene_symbol": "[\"Rpp25l\"]", "do": null }, { "gene_id": 69976, "description": "galactokinase 2", "gene_symbol": "[\"Galk2\"]", "do": null }, { "gene_id": 69981, "description": "cell division cycle 50 P4-ATPase accessory subunit A", "gene_symbol": "[\"Cdc50a\"]", "do": null }, { "gene_id": 69983, "description": "sucrase isomaltase", "gene_symbol": "[\"Sis\"]", "do": null }, { "gene_id": 70008, "description": "angiotensin converting enzyme 2", "gene_symbol": "[\"Ace2\"]", "do": "[{\"label\":\"COVID-19\",\"id\":\"DOID:0080600\"},{\"label\":\"congestive heart failure\",\"id\":\"DOID:6000\"}]" }, { "gene_id": 70028, "description": "DOP1 leucine zipper like protein B", "gene_symbol": "[\"Dop1b\"]", "do": null }, { "gene_id": 70086, "description": "cysteinyl leukotriene receptor 2", "gene_symbol": "[\"Cysltr2\"]", "do": null }, { "gene_id": 70097, "description": "SAM and SH3 domain containing 1", "gene_symbol": "[\"Sash1\"]", "do": null }, { "gene_id": 70129, "description": "solute carrier family 44, member 4", "gene_symbol": "[\"Slc44a4\"]", "do": null }, { "gene_id": 70144, "description": "leucine-rich repeats and calponin homology (CH) domain containing 3", "gene_symbol": "[\"Lrch3\"]", "do": null }, { "gene_id": 70155, "description": "opioid growth factor receptor-like 1", "gene_symbol": "[\"Ogfrl1\"]", "do": null }, { "gene_id": 70160, "description": "vacuolar protein sorting 36", "gene_symbol": "[\"Vps36\"]", "do": null }, { "gene_id": 70163, "description": "LY6/PLAUR domain containing 8", "gene_symbol": "[\"Lypd8\"]", "do": null }, { "gene_id": 70166, "description": "lipase family member N", "gene_symbol": "[\"Lipn\"]", "do": null }, { "gene_id": 70186, "description": "family with sequence similarity 162, member A", "gene_symbol": "[\"Fam162a\"]", "do": null }, { "gene_id": 70231, "description": "golgi reassembly stacking protein 2", "gene_symbol": "[\"Gorasp2\"]", "do": null }, { "gene_id": 70247, "description": "proteasome (prosome, macropain) 26S subunit, non-ATPase, 1", "gene_symbol": "[\"Psmd1\"]", "do": null }, { "gene_id": 70325, "description": "phosphatidylinositol glycan anchor biosynthesis, class W", "gene_symbol": "[\"Pigw\"]", "do": null }, { "gene_id": 70335, "description": "receptor accessory protein 6", "gene_symbol": "[\"Reep6\"]", "do": "[{\"label\":\"retinitis pigmentosa 77\",\"id\":\"DOID:0080350\"}]" }, { "gene_id": 70349, "description": "coatomer protein complex, subunit beta 1", "gene_symbol": "[\"Copb1\"]", "do": null }, { "gene_id": 70350, "description": "brain abundant, membrane attached signal protein 1", "gene_symbol": "[\"Basp1\"]", "do": null }, { "gene_id": 70351, "description": "protein phosphatase 4, regulatory subunit 1", "gene_symbol": "[\"Ppp4r1\"]", "do": null }, { "gene_id": 70355, "description": "G protein-coupled receptor, family C, group 5, member C", "gene_symbol": "[\"Gprc5c\"]", "do": null }, { "gene_id": 70361, "description": "lectin, mannose-binding, 1", "gene_symbol": "[\"Lman1\"]", "do": null }, { "gene_id": 70363, "description": "family with sequence similarity 135, member B", "gene_symbol": "[\"Fam135b\"]", "do": null }, { "gene_id": 70370, "description": "fibulin 7", "gene_symbol": "[\"Fbln7\"]", "do": null }, { "gene_id": 70381, "description": "tectonin beta-propeller repeat containing 1", "gene_symbol": "[\"Tecpr1\"]", "do": null }, { "gene_id": 70417, "description": "multiple EGF-like-domains 10", "gene_symbol": "[\"Megf10\"]", "do": null }, { "gene_id": 70422, "description": "integrator complex subunit 2", "gene_symbol": "[\"Ints2\"]", "do": null }, { "gene_id": 70423, "description": "tetraspanin 15", "gene_symbol": "[\"Tspan15\"]", "do": null }, { "gene_id": 70433, "description": "dorsal inhibitory axon guidance protein", "gene_symbol": "[\"Draxin\"]", "do": null }, { "gene_id": 70435, "description": "inverted formin, FH2 and WH2 domain containing", "gene_symbol": "[\"Inf2\"]", "do": null }, { "gene_id": 70445, "description": "CD248 antigen, endosialin", "gene_symbol": "[\"Cd248\"]", "do": null }, { "gene_id": 70456, "description": "mitochondrial pyruvate carrier 2", "gene_symbol": "[\"Mpc2\"]", "do": null }, { "gene_id": 70465, "description": "WD repeat domain 77", "gene_symbol": "[\"Wdr77\"]", "do": null }, { "gene_id": 70466, "description": "cytoskeleton associated protein 2-like", "gene_symbol": "[\"Ckap2l\"]", "do": null }, { "gene_id": 70472, "description": "ATPase family, AAA domain containing 2", "gene_symbol": "[\"Atad2\"]", "do": null }, { "gene_id": 70497, "description": "Rho GTPase activating protein 17", "gene_symbol": "[\"Arhgap17\"]", "do": null }, { "gene_id": 70510, "description": "ring finger protein 167", "gene_symbol": "[\"Rnf167\"]", "do": null }, { "gene_id": 70530, "description": "leucine rich repeat and fibronectin type III domain containing 2", "gene_symbol": "[\"Lrfn2\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 70536, "description": "glutaminyl-peptide cyclotransferase (glutaminyl cyclase)", "gene_symbol": "[\"Qpct\"]", "do": null }, { "gene_id": 70549, "description": "talin 2", "gene_symbol": "[\"Tln2\"]", "do": null }, { "gene_id": 70551, "description": "transmembrane and tetratricopeptide repeat containing 4", "gene_symbol": "[\"Tmtc4\"]", "do": null }, { "gene_id": 70561, "description": "thioredoxin domain containing 16", "gene_symbol": "[\"Txndc16\"]", "do": null }, { "gene_id": 70574, "description": "carboxypeptidase M", "gene_symbol": "[\"Cpm\"]", "do": null }, { "gene_id": 70575, "description": "glucose-fructose oxidoreductase domain containing 2", "gene_symbol": "[\"Gfod2\"]", "do": null }, { "gene_id": 70598, "description": "filamin A interacting protein 1", "gene_symbol": "[\"Filip1\"]", "do": null }, { "gene_id": 70601, "description": "ecdysoneless cell cycle regulator", "gene_symbol": "[\"Ecd\"]", "do": null }, { "gene_id": 70603, "description": "mutY DNA glycosylase", "gene_symbol": "[\"Mutyh\"]", "do": null }, { "gene_id": 70616, "description": "SURP and G patch domain containing 1", "gene_symbol": "[\"Sugp1\"]", "do": null }, { "gene_id": 70620, "description": "ubiquitin-conjugating enzyme E2 variant 2", "gene_symbol": "[\"Ube2v2\"]", "do": null }, { "gene_id": 70650, "description": "zinc finger, CCHC domain containing 8", "gene_symbol": "[\"Zcchc8\"]", "do": null }, { "gene_id": 70661, "description": "SIK family kinase 3", "gene_symbol": "[\"Sik3\"]", "do": null }, { "gene_id": 70675, "description": "valosin containing protein (p97)/p47 complex interacting protein 1", "gene_symbol": "[\"Vcpip1\"]", "do": "[{\"label\":\"progeria\",\"id\":\"DOID:3911\"}]" }, { "gene_id": 70693, "description": "adhesion G protein-coupled receptor A3", "gene_symbol": "[\"Adgra3\"]", "do": null }, { "gene_id": 70701, "description": "NIPA-like domain containing 1", "gene_symbol": "[\"Nipal1\"]", "do": null }, { "gene_id": 70719, "description": "Rho GTPase activating protein 45", "gene_symbol": "[\"Arhgap45\"]", "do": null }, { "gene_id": 70726, "description": "angiopoietin-like 6", "gene_symbol": "[\"Angptl6\"]", "do": "[{\"label\":\"obesity\",\"id\":\"DOID:9970\"}]" }, { "gene_id": 70737, "description": "cingulin", "gene_symbol": "[\"Cgn\"]", "do": null }, { "gene_id": 70747, "description": "tetraspanin 2", "gene_symbol": "[\"Tspan2\"]", "do": null }, { "gene_id": 70757, "description": "3-hydroxyacyl-CoA dehydratase 2", "gene_symbol": "[\"Hacd2\"]", "do": null }, { "gene_id": 70771, "description": "G-protein coupled receptor 173", "gene_symbol": "[\"Gpr173\"]", "do": null }, { "gene_id": 70797, "description": "ankyrin repeat and IBR domain containing 1", "gene_symbol": "[\"Ankib1\"]", "do": null }, { "gene_id": 70804, "description": "progesterone receptor membrane component 2", "gene_symbol": "[\"Pgrmc2\"]", "do": null }, { "gene_id": 70809, "description": "C-type lectin domain family 2, member g", "gene_symbol": "[\"Clec2g\"]", "do": null }, { "gene_id": 70827, "description": "trafficking protein, kinesin binding 2", "gene_symbol": "[\"Trak2\"]", "do": null }, { "gene_id": 70834, "description": "sperm associated antigen 9", "gene_symbol": "[\"Spag9\"]", "do": null }, { "gene_id": 70835, "description": "serine protease 22", "gene_symbol": "[\"Prss22\"]", "do": null }, { "gene_id": 70839, "description": "purinergic receptor P2Y, G-protein coupled 12", "gene_symbol": "[\"P2ry12\"]", "do": "[{\"label\":\"platelet-type bleeding disorder 8\",\"id\":\"DOID:0060692\"}]" }, { "gene_id": 70840, "description": "solute carrier family 22 (organic cation transporter), member 16", "gene_symbol": "[\"Slc22a16\"]", "do": null }, { "gene_id": 70866, "description": "solute carrier organic anion transporter family, member 6d1", "gene_symbol": "[\"Slco6d1\"]", "do": null }, { "gene_id": 70884, "description": "coiled-coil domain containing 81", "gene_symbol": "[\"Ccdc81\"]", "do": null }, { "gene_id": 70893, "description": "galactosidase, beta 1 like 3", "gene_symbol": "[\"Glb1l3\"]", "do": null }, { "gene_id": 70902, "description": "lysophosphatidylcholine acyltransferase 2B", "gene_symbol": "[\"Lpcat2b\"]", "do": null }, { "gene_id": 70911, "description": "phytanoyl-CoA hydroxylase interacting protein-like", "gene_symbol": "[\"Phyhipl\"]", "do": null }, { "gene_id": 70918, "description": "NOL1/NOP2/Sun domain family, member 7", "gene_symbol": "[\"Nsun7\"]", "do": null }, { "gene_id": 70925, "description": "CDKN2A interacting protein", "gene_symbol": "[\"Cdkn2aip\"]", "do": null }, { "gene_id": 70945, "description": "multimerin 1", "gene_symbol": "[\"Mmrn1\"]", "do": null }, { "gene_id": 70967, "description": "eva-1 homolog C", "gene_symbol": "[\"Eva1c\"]", "do": null }, { "gene_id": 70974, "description": "phosphoglucomutase 2-like 1", "gene_symbol": "[\"Pgm2l1\"]", "do": null }, { "gene_id": 70977, "description": "calcium binding protein, spermatid specific 1", "gene_symbol": "[\"Cabs1\"]", "do": null }, { "gene_id": 71001, "description": "MGAT4 family, member E", "gene_symbol": "[\"Mgat4e\"]", "do": null }, { "gene_id": 71003, "description": "serine protease 41", "gene_symbol": "[\"Prss41\"]", "do": null }, { "gene_id": 71020, "description": "spermatogenesis associated, serine-rich 1", "gene_symbol": "[\"Spats1\"]", "do": null }, { "gene_id": 71027, "description": "Cdc50 family member C", "gene_symbol": "[\"Cdc50c\"]", "do": null }, { "gene_id": 71037, "description": "serine protease 55", "gene_symbol": "[\"Prss55\"]", "do": null }, { "gene_id": 71062, "description": "tektin 3", "gene_symbol": "[\"Tekt3\"]", "do": null }, { "gene_id": 71069, "description": "storkhead box 2", "gene_symbol": "[\"Stox2\"]", "do": null }, { "gene_id": 71088, "description": "RIKEN cDNA 4933412E24 gene", "gene_symbol": "[\"4933412E24Rik\"]", "do": null }, { "gene_id": 71103, "description": "glycosyltransferase 6 domain containing 1", "gene_symbol": "[\"Glt6d1\"]", "do": null }, { "gene_id": 71111, "description": "G protein-coupled receptor 39", "gene_symbol": "[\"Gpr39\"]", "do": null }, { "gene_id": 71145, "description": "scavenger receptor class A, member 5", "gene_symbol": "[\"Scara5\"]", "do": null }, { "gene_id": 71175, "description": "NIPBL cohesin loading factor", "gene_symbol": "[\"Nipbl\"]", "do": "[{\"label\":\"Cornelia de Lange syndrome 1\",\"id\":\"DOID:0080505\"}]" }, { "gene_id": 71183, "description": "C-type lectin domain family 12, member B", "gene_symbol": "[\"Clec12b\"]", "do": null }, { "gene_id": 71279, "description": "solute carrier family 29 (nucleoside transporters), member 3", "gene_symbol": "[\"Slc29a3\"]", "do": null }, { "gene_id": 71287, "description": "carboxypeptidase, vitellogenic-like", "gene_symbol": "[\"Cpvl\"]", "do": null }, { "gene_id": 71300, "description": "ring finger protein 148", "gene_symbol": "[\"Rnf148\"]", "do": null }, { "gene_id": 71302, "description": "Rho GTPase activating protein 26", "gene_symbol": "[\"Arhgap26\"]", "do": null }, { "gene_id": 71306, "description": "microfibrillar-associated protein 3-like", "gene_symbol": "[\"Mfap3l\"]", "do": null }, { "gene_id": 71310, "description": "TBC1 domain family, member 9", "gene_symbol": "[\"Tbc1d9\"]", "do": null }, { "gene_id": 71336, "description": "ribokinase", "gene_symbol": "[\"Rbks\"]", "do": null }, { "gene_id": 71345, "description": "anoctamin 9", "gene_symbol": "[\"Ano9\"]", "do": null }, { "gene_id": 71355, "description": "collagen, type XXIV, alpha 1", "gene_symbol": "[\"Col24a1\"]", "do": null }, { "gene_id": 71367, "description": "carbohydrate sulfotransferase 9", "gene_symbol": "[\"Chst9\"]", "do": null }, { "gene_id": 71371, "description": "AT-rich interaction domain 5B", "gene_symbol": "[\"Arid5b\"]", "do": null }, { "gene_id": 71389, "description": "chromodomain helicase DNA binding protein 6", "gene_symbol": "[\"Chd6\"]", "do": null }, { "gene_id": 71395, "description": "CUB domain containing protein 3", "gene_symbol": "[\"Cdcp3\"]", "do": null }, { "gene_id": 71425, "description": "BPI fold containing family B, member 9A", "gene_symbol": "[\"Bpifb9a\"]", "do": null }, { "gene_id": 71435, "description": "Rho GTPase activating protein 21", "gene_symbol": "[\"Arhgap21\"]", "do": null }, { "gene_id": 71436, "description": "fibronectin leucine rich transmembrane protein 3", "gene_symbol": "[\"Flrt3\"]", "do": null }, { "gene_id": 71452, "description": "ankyrin repeat domain 40", "gene_symbol": "[\"Ankrd40\"]", "do": null }, { "gene_id": 71458, "description": "BCL6 interacting corepressor", "gene_symbol": "[\"Bcor\"]", "do": "[{\"label\":\"syndromic microphthalmia 2\",\"id\":\"DOID:0111809\"}]" }, { "gene_id": 71461, "description": "PTK7 protein tyrosine kinase 7", "gene_symbol": "[\"Ptk7\"]", "do": null }, { "gene_id": 71514, "description": "splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)", "gene_symbol": "[\"Sfpq\"]", "do": null }, { "gene_id": 71517, "description": "VPS35 endosomal protein sorting factor like", "gene_symbol": "[\"Vps35l\"]", "do": null }, { "gene_id": 71522, "description": "gamma-glutamyltransferase 6", "gene_symbol": "[\"Ggt6\"]", "do": null }, { "gene_id": 71529, "description": "kazrin, periplakin interacting protein", "gene_symbol": "[\"Kazn\"]", "do": null }, { "gene_id": 71544, "description": "Rho GTPase activating protein 42", "gene_symbol": "[\"Arhgap42\"]", "do": null }, { "gene_id": 71564, "description": "IZUMO family member 4", "gene_symbol": "[\"Izumo4\"]", "do": null }, { "gene_id": 71566, "description": "CXADR-like membrane protein", "gene_symbol": "[\"Clmp\"]", "do": null }, { "gene_id": 71584, "description": "glycerophosphodiester phosphodiesterase domain containing 2", "gene_symbol": "[\"Gdpd2\"]", "do": null }, { "gene_id": 71601, "description": "CEA cell adhesion molecule 20", "gene_symbol": "[\"Ceacam20\"]", "do": null }, { "gene_id": 71609, "description": "TNFRSF1A-associated via death domain", "gene_symbol": "[\"Tradd\"]", "do": null }, { "gene_id": 71640, "description": "zinc finger protein 949", "gene_symbol": "[\"Zfp949\"]", "do": null }, { "gene_id": 71665, "description": "fucosidase, alpha-L- 1, tissue", "gene_symbol": "[\"Fuca1\"]", "do": "[{\"label\":\"fucosidosis\",\"id\":\"DOID:14500\"}]" }, { "gene_id": 71667, "description": "transmembrane protein 248", "gene_symbol": "[\"Tmem248\"]", "do": null }, { "gene_id": 71673, "description": "ring finger protein 215", "gene_symbol": "[\"Rnf215\"]", "do": null }, { "gene_id": 71685, "description": "polypeptide N-acetylgalactosaminyltransferase 14", "gene_symbol": "[\"Galnt14\"]", "do": null }, { "gene_id": 71687, "description": "transmembrane protein 25", "gene_symbol": "[\"Tmem25\"]", "do": null }, { "gene_id": 71690, "description": "endothelial cell-specific molecule 1", "gene_symbol": "[\"Esm1\"]", "do": null }, { "gene_id": 71701, "description": "polyribonucleotide nucleotidyltransferase 1", "gene_symbol": "[\"Pnpt1\"]", "do": null }, { "gene_id": 71702, "description": "cell division cycle 5-like", "gene_symbol": "[\"Cdc5l\"]", "do": null }, { "gene_id": 71706, "description": "solute carrier family 46, member 3", "gene_symbol": "[\"Slc46a3\"]", "do": null }, { "gene_id": 71718, "description": "telomere maintenance 2", "gene_symbol": "[\"Telo2\"]", "do": null }, { "gene_id": 71722, "description": "capicua transcriptional repressor", "gene_symbol": "[\"Cic\"]", "do": "[{\"label\":\"disease of mental health\",\"id\":\"DOID:150\"}]" }, { "gene_id": 71726, "description": "single-strand selective monofunctional uracil DNA glycosylase", "gene_symbol": "[\"Smug1\"]", "do": null }, { "gene_id": 71729, "description": "regulator of G-protein signaling 12", "gene_symbol": "[\"Rgs12\"]", "do": null }, { "gene_id": 71733, "description": "sushi domain containing 2", "gene_symbol": "[\"Susd2\"]", "do": null }, { "gene_id": 71738, "description": "MAM domain containing 2", "gene_symbol": "[\"Mamdc2\"]", "do": null }, { "gene_id": 71740, "description": "nectin cell adhesion molecule 4", "gene_symbol": "[\"Nectin4\"]", "do": null }, { "gene_id": 71745, "description": "cullin 2", "gene_symbol": "[\"Cul2\"]", "do": null }, { "gene_id": 71750, "description": "R3H domain containing 2", "gene_symbol": "[\"R3hdm2\"]", "do": null }, { "gene_id": 71751, "description": "mitogen-activated protein kinase kinase kinase 13", "gene_symbol": "[\"Map3k13\"]", "do": null }, { "gene_id": 71753, "description": "transmembrane serine protease 6", "gene_symbol": "[\"Tmprss6\"]", "do": null }, { "gene_id": 71755, "description": "dihydrodiol dehydrogenase", "gene_symbol": "[\"Dhdh\"]", "do": null }, { "gene_id": 71756, "description": "carboxypeptidase N, polypeptide 2", "gene_symbol": "[\"Cpn2\"]", "do": null }, { "gene_id": 71764, "description": "C2 calcium-dependent domain containing 2-like", "gene_symbol": "[\"C2cd2l\"]", "do": null }, { "gene_id": 71768, "description": "von Willebrand factor C and EGF domains", "gene_symbol": "[\"Vwce\"]", "do": null }, { "gene_id": 71770, "description": "adaptor-related protein complex 2, beta 1 subunit", "gene_symbol": "[\"Ap2b1\"]", "do": null }, { "gene_id": 71772, "description": "phospholipase B domain containing 2", "gene_symbol": "[\"Plbd2\"]", "do": null }, { "gene_id": 71773, "description": "UDP glucuronosyltransferase 2 family, polypeptide B1", "gene_symbol": "[\"Ugt2b1\"]", "do": null }, { "gene_id": 71774, "description": "shroom family member 1", "gene_symbol": "[\"Shroom1\"]", "do": null }, { "gene_id": 71775, "description": "inhibitor of carbonic anhydrase", "gene_symbol": "[\"Inhca\"]", "do": null }, { "gene_id": 71785, "description": "platelet-derived growth factor, D polypeptide", "gene_symbol": "[\"Pdgfd\"]", "do": null }, { "gene_id": 71791, "description": "carboxypeptidase A4", "gene_symbol": "[\"Cpa4\"]", "do": null }, { "gene_id": 71797, "description": "carbohydrate sulfotransferase 13", "gene_symbol": "[\"Chst13\"]", "do": null }, { "gene_id": 71819, "description": "kinesin family member 23", "gene_symbol": "[\"Kif23\"]", "do": null }, { "gene_id": 71830, "description": "protein disulfide isomerase-like, testis expressed", "gene_symbol": "[\"Pdilt\"]", "do": null }, { "gene_id": 71832, "description": "citrate synthase like", "gene_symbol": "[\"Csl\"]", "do": null }, { "gene_id": 71833, "description": "DDB1 and CUL4 associated factor 7", "gene_symbol": "[\"Dcaf7\"]", "do": null }, { "gene_id": 71835, "description": "LanC (bacterial lantibiotic synthetase component C)-like 2", "gene_symbol": "[\"Lancl2\"]", "do": null }, { "gene_id": 71844, "description": "nucleoporin 58", "gene_symbol": "[\"Nup58\"]", "do": null }, { "gene_id": 71853, "description": "protein disulfide isomerase associated 6", "gene_symbol": "[\"Pdia6\"]", "do": null }, { "gene_id": 71854, "description": "dipeptidase 3", "gene_symbol": "[\"Dpep3\"]", "do": null }, { "gene_id": 71856, "description": "WAP four-disulfide core domain 3", "gene_symbol": "[\"Wfdc3\"]", "do": null }, { "gene_id": 71862, "description": "G protein-coupled receptor 160", "gene_symbol": "[\"Gpr160\"]", "do": null }, { "gene_id": 71865, "description": "F-box protein 30", "gene_symbol": "[\"Fbxo30\"]", "do": null }, { "gene_id": 71874, "description": "mab-21-like 4", "gene_symbol": "[\"Mab21l4\"]", "do": null }, { "gene_id": 71881, "description": "adipocyte plasma membrane associated protein", "gene_symbol": "[\"Apmap\"]", "do": null }, { "gene_id": 71883, "description": "coenzyme Q2 4-hydroxybenzoate polyprenyltransferase", "gene_symbol": "[\"Coq2\"]", "do": null }, { "gene_id": 71884, "description": "chitinase 1", "gene_symbol": "[\"Chit1\"]", "do": null }, { "gene_id": 71886, "description": "RIKEN cDNA 2310002L09 gene", "gene_symbol": "[\"2310002L09Rik\"]", "do": null }, { "gene_id": 71900, "description": "transmembrane protein 106B", "gene_symbol": "[\"Tmem106b\"]", "do": null }, { "gene_id": 71902, "description": "cullin associated and neddylation disassociated 1", "gene_symbol": "[\"Cand1\"]", "do": null }, { "gene_id": 71907, "description": "serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 9", "gene_symbol": "[\"Serpina9\"]", "do": null }, { "gene_id": 71911, "description": "3-hydroxybutyrate dehydrogenase, type 1", "gene_symbol": "[\"Bdh1\"]", "do": null }, { "gene_id": 71914, "description": "anthrax toxin receptor 2", "gene_symbol": "[\"Antxr2\"]", "do": null }, { "gene_id": 71918, "description": "zinc finger, CCHC domain containing 24", "gene_symbol": "[\"Zcchc24\"]", "do": null }, { "gene_id": 71920, "description": "epithelial mitogen", "gene_symbol": "[\"Epgn\"]", "do": null }, { "gene_id": 71927, "description": "integrin alpha FG-GAP repeat containing 1", "gene_symbol": "[\"Itfg1\"]", "do": null }, { "gene_id": 71929, "description": "transmembrane protein 123", "gene_symbol": "[\"Tmem123\"]", "do": null }, { "gene_id": 71943, "description": "target of myb1-like 1 (chicken)", "gene_symbol": "[\"Tom1l1\"]", "do": null }, { "gene_id": 71947, "description": "transmembrane protein 94", "gene_symbol": "[\"Tmem94\"]", "do": null }, { "gene_id": 71949, "description": "ceramide synthase 5", "gene_symbol": "[\"Cers5\"]", "do": null }, { "gene_id": 71950, "description": "Nanog homeobox", "gene_symbol": "[\"Nanog\"]", "do": null }, { "gene_id": 71951, "description": "glypican 2 cerebroglycan", "gene_symbol": "[\"Gpc2\"]", "do": null }, { "gene_id": 71972, "description": "dynamin binding protein", "gene_symbol": "[\"Dnmbp\"]", "do": null }, { "gene_id": 71984, "description": "seryl-aminoacyl-tRNA synthetase 2", "gene_symbol": "[\"Sars2\"]", "do": null }, { "gene_id": 71994, "description": "calponin 3, acidic", "gene_symbol": "[\"Cnn3\"]", "do": null }, { "gene_id": 72002, "description": "solute carrier family 39 (metal ion transporter), member 5", "gene_symbol": "[\"Slc39a5\"]", "do": null }, { "gene_id": 72003, "description": "synaptoporin", "gene_symbol": "[\"Synpr\"]", "do": null }, { "gene_id": 72014, "description": "BTB domain containing 17", "gene_symbol": "[\"Btbd17\"]", "do": null }, { "gene_id": 72027, "description": "solute carrier family 39 (zinc transporter), member 4", "gene_symbol": "[\"Slc39a4\"]", "do": "[{\"label\":\"acrodermatitis enteropathica\",\"id\":\"DOID:0050605\"}]" }, { "gene_id": 72029, "description": "canopy FGF signaling regulator 3", "gene_symbol": "[\"Cnpy3\"]", "do": null }, { "gene_id": 72033, "description": "TSC22 domain family, member 2", "gene_symbol": "[\"Tsc22d2\"]", "do": null }, { "gene_id": 72039, "description": "methylcrotonoyl-Coenzyme A carboxylase 1 (alpha)", "gene_symbol": "[\"Mccc1\"]", "do": null }, { "gene_id": 72040, "description": "cadherin-related family member 5", "gene_symbol": "[\"Cdhr5\"]", "do": null }, { "gene_id": 72043, "description": "sulfatase 2", "gene_symbol": "[\"Sulf2\"]", "do": null }, { "gene_id": 72047, "description": "DEAD box helicase 42", "gene_symbol": "[\"Ddx42\"]", "do": null }, { "gene_id": 72049, "description": "tumor necrosis factor receptor superfamily, member 13c", "gene_symbol": "[\"Tnfrsf13c\"]", "do": null }, { "gene_id": 72050, "description": "protein O-glucosyltransferase 2", "gene_symbol": "[\"Poglut2\"]", "do": null }, { "gene_id": 72056, "description": "RIKEN cDNA 1810055G02 gene", "gene_symbol": "[\"1810055G02Rik\"]", "do": null }, { "gene_id": 72057, "description": "PHD finger protein 10", "gene_symbol": "[\"Phf10\"]", "do": null }, { "gene_id": 72058, "description": "immunoglobulin superfamily, member 5", "gene_symbol": "[\"Igsf5\"]", "do": null }, { "gene_id": 72068, "description": "CCR4-NOT transcription complex, subunit 2", "gene_symbol": "[\"Cnot2\"]", "do": null }, { "gene_id": 72075, "description": "opioid growth factor receptor", "gene_symbol": "[\"Ogfr\"]", "do": null }, { "gene_id": 72077, "description": "glucosaminyl (N-acetyl) transferase 3, mucin type", "gene_symbol": "[\"Gcnt3\"]", "do": null }, { "gene_id": 72083, "description": "mitotic spindle organizing protein 2", "gene_symbol": "[\"Mzt2\"]", "do": null }, { "gene_id": 72084, "description": "phosphatidylinositol glycan anchor biosynthesis, class X", "gene_symbol": "[\"Pigx\"]", "do": null }, { "gene_id": 72090, "description": "ectonucleoside triphosphate diphosphohydrolase 8", "gene_symbol": "[\"Entpd8\"]", "do": null }, { "gene_id": 72094, "description": "UDP glucuronosyltransferase 2 family, polypeptide A3", "gene_symbol": "[\"Ugt2a3\"]", "do": null }, { "gene_id": 72097, "description": "capping protein inhibiting regulator of actin like", "gene_symbol": "[\"Cracdl\"]", "do": null }, { "gene_id": 72098, "description": "transmembrane protein 68", "gene_symbol": "[\"Tmem68\"]", "do": null }, { "gene_id": 72106, "description": "jumonji domain containing 8", "gene_symbol": "[\"Jmjd8\"]", "do": null }, { "gene_id": 72113, "description": "aarF domain containing kinase 1", "gene_symbol": "[\"Adck1\"]", "do": null }, { "gene_id": 72136, "description": "carbohydrate sulfotransferase 14", "gene_symbol": "[\"Chst14\"]", "do": null }, { "gene_id": 72141, "description": "ADP-dependent glucokinase", "gene_symbol": "[\"Adpgk\"]", "do": null }, { "gene_id": 72144, "description": "solute carrier family 37 (glycerol-3-phosphate transporter), member 3", "gene_symbol": "[\"Slc37a3\"]", "do": null }, { "gene_id": 72145, "description": "WD repeat and FYVE domain containing 3", "gene_symbol": "[\"Wdfy3\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 72157, "description": "phosphoglucomutase 1", "gene_symbol": "[\"Pgm1\"]", "do": null }, { "gene_id": 72160, "description": "transmembrane protein 163", "gene_symbol": "[\"Tmem163\"]", "do": null }, { "gene_id": 72162, "description": "DEAH-box helicase 36", "gene_symbol": "[\"Dhx36\"]", "do": null }, { "gene_id": 72175, "description": "major facilitator superfamily domain containing 8", "gene_symbol": "[\"Mfsd8\"]", "do": "[{\"label\":\"neuronal ceroid lipofuscinosis 7\",\"id\":\"DOID:0110722\"}]" }, { "gene_id": 72183, "description": "sorting nexin 6", "gene_symbol": "[\"Snx6\"]", "do": null }, { "gene_id": 72184, "description": "kelch-like 35", "gene_symbol": "[\"Klhl35\"]", "do": null }, { "gene_id": 72238, "description": "TBC1 domain family, member 5", "gene_symbol": "[\"Tbc1d5\"]", "do": null }, { "gene_id": 72242, "description": "pregnancy-specific beta-1-glycoprotein 21", "gene_symbol": "[\"Psg21\"]", "do": null }, { "gene_id": 72265, "description": "translocating chain-associating membrane protein 1", "gene_symbol": "[\"Tram1\"]", "do": null }, { "gene_id": 72267, "description": "leucine rich repeat containing 8 family, member E", "gene_symbol": "[\"Lrrc8e\"]", "do": null }, { "gene_id": 72275, "description": "RIKEN cDNA 2200002D01 gene", "gene_symbol": "[\"2200002D01Rik\"]", "do": null }, { "gene_id": 72278, "description": "cell cycle progression 1", "gene_symbol": "[\"Ccpg1\"]", "do": null }, { "gene_id": 72281, "description": "SH2 domain containing 4A", "gene_symbol": "[\"Sh2d4a\"]", "do": null }, { "gene_id": 72297, "description": "UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3", "gene_symbol": "[\"B3gnt3\"]", "do": null }, { "gene_id": 72301, "description": "shisa like 1", "gene_symbol": "[\"Shisal1\"]", "do": null }, { "gene_id": 72324, "description": "plexin domain containing 1", "gene_symbol": "[\"Plxdc1\"]", "do": null }, { "gene_id": 72333, "description": "palladin, cytoskeletal associated protein", "gene_symbol": "[\"Palld\"]", "do": null }, { "gene_id": 72344, "description": "ubiquitin specific peptidase 36", "gene_symbol": "[\"Usp36\"]", "do": null }, { "gene_id": 72357, "description": "RIKEN cDNA 2210016L21 gene", "gene_symbol": "[\"2210016L21Rik\"]", "do": null }, { "gene_id": 72361, "description": "carboxylesterase 2G", "gene_symbol": "[\"Ces2g\"]", "do": null }, { "gene_id": 72373, "description": "prostate stem cell antigen", "gene_symbol": "[\"Psca\"]", "do": null }, { "gene_id": 72393, "description": "Fas apoptotic inhibitory molecule 2", "gene_symbol": "[\"Faim2\"]", "do": null }, { "gene_id": 72401, "description": "solute carrier family 43, member 1", "gene_symbol": "[\"Slc43a1\"]", "do": null }, { "gene_id": 72413, "description": "potassium large conductance calcium-activated channel, subfamily M, beta member 2", "gene_symbol": "[\"Kcnmb2\"]", "do": null }, { "gene_id": 72416, "description": "leucine-rich PPR-motif containing", "gene_symbol": "[\"Lrpprc\"]", "do": null }, { "gene_id": 72431, "description": "CEA cell adhesion molecule 18", "gene_symbol": "[\"Ceacam18\"]", "do": null }, { "gene_id": 72432, "description": "serine peptidase inhibitor, Kazal type 5", "gene_symbol": "[\"Spink5\"]", "do": "[{\"label\":\"Netherton syndrome\",\"id\":\"DOID:0050474\"}]" }, { "gene_id": 72434, "description": "Ly6/Plaur domain containing 3", "gene_symbol": "[\"Lypd3\"]", "do": null }, { "gene_id": 72461, "description": "prolylcarboxypeptidase (angiotensinase C)", "gene_symbol": "[\"Prcp\"]", "do": null }, { "gene_id": 72475, "description": "single-stranded DNA binding protein 3", "gene_symbol": "[\"Ssbp3\"]", "do": null }, { "gene_id": 72477, "description": "transmembrane protein 87B", "gene_symbol": "[\"Tmem87b\"]", "do": null }, { "gene_id": 72504, "description": "TATA-box binding protein associated factor 4b", "gene_symbol": "[\"Taf4b\"]", "do": null }, { "gene_id": 72508, "description": "ribosomal protein S6 kinase B1", "gene_symbol": "[\"Rps6kb1\"]", "do": null }, { "gene_id": 72535, "description": "aldehyde dehydrogenase 1 family, member B1", "gene_symbol": "[\"Aldh1b1\"]", "do": null }, { "gene_id": 72536, "description": "T cell activation Rho GTPase activating protein", "gene_symbol": "[\"Tagap\"]", "do": null }, { "gene_id": 72555, "description": "shisa family member 9", "gene_symbol": "[\"Shisa9\"]", "do": null }, { "gene_id": 72560, "description": "N-acetylated alpha-linked acidic dipeptidase 2", "gene_symbol": "[\"Naalad2\"]", "do": null }, { "gene_id": 72565, "description": "uveal autoantigen with coiled-coil domains and ankyrin repeats", "gene_symbol": "[\"Uaca\"]", "do": "[{\"label\":\"hepatocellular carcinoma\",\"id\":\"DOID:684\"}]" }, { "gene_id": 72584, "description": "cullin 4B", "gene_symbol": "[\"Cul4b\"]", "do": "[{\"label\":\"intellectual disability\",\"id\":\"DOID:1059\"}]" }, { "gene_id": 72585, "description": "Ly6/Plaur domain containing 1", "gene_symbol": "[\"Lypd1\"]", "do": null }, { "gene_id": 72587, "description": "PAN3 poly(A) specific ribonuclease subunit", "gene_symbol": "[\"Pan3\"]", "do": null }, { "gene_id": 72605, "description": "carbonic anhydrase 10", "gene_symbol": "[\"Car10\"]", "do": null }, { "gene_id": 72634, "description": "tudor and KH domain containing protein", "gene_symbol": "[\"Tdrkh\"]", "do": null }, { "gene_id": 72649, "description": "transmembrane protein 209", "gene_symbol": "[\"Tmem209\"]", "do": null }, { "gene_id": 72662, "description": "DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease", "gene_symbol": "[\"Dis3\"]", "do": null }, { "gene_id": 72685, "description": "DnaJ heat shock protein family (Hsp40) member C6", "gene_symbol": "[\"Dnajc6\"]", "do": null }, { "gene_id": 72691, "description": "calcium homeostasis modulator family member 2", "gene_symbol": "[\"Calhm2\"]", "do": null }, { "gene_id": 72692, "description": "heterogeneous nuclear ribonucleoprotein L-like", "gene_symbol": "[\"Hnrnpll\"]", "do": null }, { "gene_id": 72709, "description": "C1q and tumor necrosis factor related protein 6", "gene_symbol": "[\"C1qtnf6\"]", "do": null }, { "gene_id": 72713, "description": "angiopoietin-like 1", "gene_symbol": "[\"Angptl1\"]", "do": null }, { "gene_id": 72722, "description": "family with sequence similarity 98, member A", "gene_symbol": "[\"Fam98a\"]", "do": null }, { "gene_id": 72727, "description": "beta-1,3-glucuronyltransferase 3", "gene_symbol": "[\"B3gat3\"]", "do": null }, { "gene_id": 72729, "description": "CDC42 small effector 2", "gene_symbol": "[\"Cdc42se2\"]", "do": null }, { "gene_id": 72745, "description": "transmembrane protein 161B", "gene_symbol": "[\"Tmem161b\"]", "do": null }, { "gene_id": 72750, "description": "family with sequence similarity 117, member B", "gene_symbol": "[\"Fam117b\"]", "do": null }, { "gene_id": 72754, "description": "Rho guanine nucleotide exchange factor 10-like", "gene_symbol": "[\"Arhgef10l\"]", "do": null }, { "gene_id": 72774, "description": "nei endonuclease VIII-like 1 (E. coli)", "gene_symbol": "[\"Neil1\"]", "do": "[{\"label\":\"abdominal obesity-metabolic syndrome\",\"id\":\"DOID:0060611\"},{\"label\":\"obesity\",\"id\":\"DOID:9970\"}]" }, { "gene_id": 72776, "description": "SAS-6 centriolar assembly protein", "gene_symbol": "[\"Sass6\"]", "do": null }, { "gene_id": 72780, "description": "R-spondin 3", "gene_symbol": "[\"Rspo3\"]", "do": null }, { "gene_id": 72787, "description": "NDC1 transmembrane nucleoporin", "gene_symbol": "[\"Ndc1\"]", "do": null }, { "gene_id": 72821, "description": "sodium channel, voltage-gated, type II, beta", "gene_symbol": "[\"Scn2b\"]", "do": null }, { "gene_id": 72825, "description": "MON1 homolog A, secretory traffciking associated", "gene_symbol": "[\"Mon1a\"]", "do": null }, { "gene_id": 72831, "description": "DExH-box helicase 30", "gene_symbol": "[\"Dhx30\"]", "do": null }, { "gene_id": 72898, "description": "aspartate beta-hydroxylase domain containing 2", "gene_symbol": "[\"Asphd2\"]", "do": null }, { "gene_id": 72899, "description": "mono-ADP ribosylhydrolase 2", "gene_symbol": "[\"Macrod2\"]", "do": null }, { "gene_id": 72900, "description": "NADH:ubiquinone oxidoreductase core subunit V2", "gene_symbol": "[\"Ndufv2\"]", "do": null }, { "gene_id": 72902, "description": "sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3", "gene_symbol": "[\"Spock3\"]", "do": null }, { "gene_id": 72927, "description": "hepatocyte cell adhesion molecule", "gene_symbol": "[\"Hepacam\"]", "do": "[{\"label\":\"megalencephalic leukoencephalopathy with subcortical cysts\",\"id\":\"DOID:0080315\"}]" }, { "gene_id": 72930, "description": "protein phosphatase 2, regulatory subunit B, beta", "gene_symbol": "[\"Ppp2r2b\"]", "do": null }, { "gene_id": 72946, "description": "leucine rich repeat containing 47", "gene_symbol": "[\"Lrrc47\"]", "do": null }, { "gene_id": 72948, "description": "tubulin polymerization promoting protein", "gene_symbol": "[\"Tppp\"]", "do": null }, { "gene_id": 72949, "description": "cyclin T2", "gene_symbol": "[\"Ccnt2\"]", "do": null }, { "gene_id": 72961, "description": "solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7", "gene_symbol": "[\"Slc17a7\"]", "do": null }, { "gene_id": 72962, "description": "thymidine phosphorylase", "gene_symbol": "[\"Tymp\"]", "do": null }, { "gene_id": 72982, "description": "transmembrane protein 138", "gene_symbol": "[\"Tmem138\"]", "do": null }, { "gene_id": 73010, "description": "G protein-coupled receptor 22", "gene_symbol": "[\"Gpr22\"]", "do": null }, { "gene_id": 73016, "description": "kringle containing transmembrane protein 2", "gene_symbol": "[\"Kremen2\"]", "do": null }, { "gene_id": 73068, "description": "protein O-fucosyltransferase 4", "gene_symbol": "[\"Pofut4\"]", "do": null }, { "gene_id": 73072, "description": "proline rich 36", "gene_symbol": "[\"Prr36\"]", "do": null }, { "gene_id": 73078, "description": "peptidase (mitochondrial processing) beta", "gene_symbol": "[\"Pmpcb\"]", "do": null }, { "gene_id": 73094, "description": "SH3-domain GRB2-like (endophilin) interacting protein 1", "gene_symbol": "[\"Sgip1\"]", "do": null }, { "gene_id": 73095, "description": "solute carrier family 25, member 42", "gene_symbol": "[\"Slc25a42\"]", "do": null }, { "gene_id": 73102, "description": "solute carrier family 22, member 23", "gene_symbol": "[\"Slc22a23\"]", "do": null }, { "gene_id": 73106, "description": "serine protease 57", "gene_symbol": "[\"Prss57\"]", "do": null }, { "gene_id": 73124, "description": "golgi integral membrane protein 4", "gene_symbol": "[\"Golim4\"]", "do": null }, { "gene_id": 73137, "description": "proline-rich coiled-coil 1", "gene_symbol": "[\"Prrc1\"]", "do": null }, { "gene_id": 73139, "description": "centromere protein V", "gene_symbol": "[\"Cenpv\"]", "do": null }, { "gene_id": 73149, "description": "C-type lectin domain family 4, member a3", "gene_symbol": "[\"Clec4a3\"]", "do": null }, { "gene_id": 73158, "description": "La ribonucleoprotein 1, translational regulator", "gene_symbol": "[\"Larp1\"]", "do": null }, { "gene_id": 73173, "description": "protocadherin 18", "gene_symbol": "[\"Pcdh18\"]", "do": null }, { "gene_id": 73182, "description": "platelet endothelial aggregation receptor 1", "gene_symbol": "[\"Pear1\"]", "do": null }, { "gene_id": 73218, "description": "signal peptide peptidase like 2B", "gene_symbol": "[\"Sppl2b\"]", "do": null }, { "gene_id": 73230, "description": "BMP-binding endothelial regulator", "gene_symbol": "[\"Bmper\"]", "do": null }, { "gene_id": 73250, "description": "CEA cell adhesion molecule 5", "gene_symbol": "[\"Ceacam5\"]", "do": null }, { "gene_id": 73316, "description": "calreticulin 3", "gene_symbol": "[\"Calr3\"]", "do": null }, { "gene_id": 73327, "description": "protease-associated domain containing 1", "gene_symbol": "[\"Pradc1\"]", "do": null }, { "gene_id": 73336, "description": "serine protease 44", "gene_symbol": "[\"Prss44\"]", "do": null }, { "gene_id": 73340, "description": "neuronal pentraxin receptor", "gene_symbol": "[\"Nptxr\"]", "do": null }, { "gene_id": 73341, "description": "Rac/Cdc42 guanine nucleotide exchange factor 6", "gene_symbol": "[\"Arhgef6\"]", "do": null }, { "gene_id": 73368, "description": "collagen, type XX, alpha 1", "gene_symbol": "[\"Col20a1\"]", "do": null }, { "gene_id": 73379, "description": "discoidin, CUB and LCCL domain containing 2", "gene_symbol": "[\"Dcbld2\"]", "do": null }, { "gene_id": 73382, "description": "serine protease 52", "gene_symbol": "[\"Prss52\"]", "do": null }, { "gene_id": 73388, "description": "BPI fold containing family A, member 3", "gene_symbol": "[\"Bpifa3\"]", "do": null }, { "gene_id": 73389, "description": "high mobility group box transcription factor 1", "gene_symbol": "[\"Hbp1\"]", "do": null }, { "gene_id": 73442, "description": "heat shock protein family A (Hsp70) member 12A", "gene_symbol": "[\"Hspa12a\"]", "do": null }, { "gene_id": 73447, "description": "WD repeat domain 13", "gene_symbol": "[\"Wdr13\"]", "do": null }, { "gene_id": 73449, "description": "small integral membrane protein 33", "gene_symbol": "[\"Smim33\"]", "do": null }, { "gene_id": 73456, "description": "izumo sperm-egg fusion 1", "gene_symbol": "[\"Izumo1\"]", "do": null }, { "gene_id": 73470, "description": "kinesin family member 2B", "gene_symbol": "[\"Kif2b\"]", "do": null }, { "gene_id": 73481, "description": "serine protease 59", "gene_symbol": "[\"Prss59\"]", "do": null }, { "gene_id": 73523, "description": "phosphatidylethanolamine binding protein 4", "gene_symbol": "[\"Pebp4\"]", "do": null }, { "gene_id": 73569, "description": "vestigial like family member 3", "gene_symbol": "[\"Vgll3\"]", "do": null }, { "gene_id": 73658, "description": "SPNS lysolipid transporter 1, lysophospholipid", "gene_symbol": "[\"Spns1\"]", "do": null }, { "gene_id": 73668, "description": "tetratricopeptide repeat domain 21B", "gene_symbol": "[\"Ttc21b\"]", "do": "[{\"label\":\"cystic kidney disease\",\"id\":\"DOID:2975\"}]" }, { "gene_id": 73694, "description": "NADH:ubiquinone oxidoreductase complex assembly factor 7", "gene_symbol": "[\"Ndufaf7\"]", "do": null }, { "gene_id": 73707, "description": "guanylate cyclase 2g", "gene_symbol": "[\"Gucy2g\"]", "do": null }, { "gene_id": 73710, "description": "tubulin, beta 2B class IIB", "gene_symbol": "[\"Tubb2b\"]", "do": "[{\"label\":\"complex cortical dysplasia with other brain malformations 7\",\"id\":\"DOID:0090132\"}]" }, { "gene_id": 73720, "description": "cystatin E/M", "gene_symbol": "[\"Cst6\"]", "do": "[{\"label\":\"autosomal recessive congenital ichthyosis 4B\",\"id\":\"DOID:0060713\"}]" }, { "gene_id": 73723, "description": "SH3 domain binding glutamic acid-rich protein-like 3", "gene_symbol": "[\"Sh3bgrl3\"]", "do": null }, { "gene_id": 73744, "description": "mannosidase, alpha, class 2C, member 1", "gene_symbol": "[\"Man2c1\"]", "do": null }, { "gene_id": 73884, "description": "zinc finger, DBF-type containing 2", "gene_symbol": "[\"Zdbf2\"]", "do": null }, { "gene_id": 74006, "description": "dynamin 1-like", "gene_symbol": "[\"Dnm1l\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 74008, "description": "arylsulfatase G", "gene_symbol": "[\"Arsg\"]", "do": "[{\"label\":\"mucopolysaccharidosis\",\"id\":\"DOID:12798\"}]" }, { "gene_id": 74011, "description": "solute carrier family 25, member 27", "gene_symbol": "[\"Slc25a27\"]", "do": null }, { "gene_id": 74018, "description": "alsin Rho guanine nucleotide exchange factor", "gene_symbol": "[\"Als2\"]", "do": null }, { "gene_id": 74022, "description": "glyoxylate reductase 1 homolog (Arabidopsis)", "gene_symbol": "[\"Glyr1\"]", "do": "[{\"label\":\"atrioventricular septal defect\",\"id\":\"DOID:0050651\"}]" }, { "gene_id": 74026, "description": "male specific lethal 1", "gene_symbol": "[\"Msl1\"]", "do": null }, { "gene_id": 74035, "description": "nucleolar protein 9", "gene_symbol": "[\"Nol9\"]", "do": null }, { "gene_id": 74039, "description": "Nfat activating molecule with ITAM motif 1", "gene_symbol": "[\"Nfam1\"]", "do": null }, { "gene_id": 74048, "description": "V-set immunoregulatory receptor", "gene_symbol": "[\"Vsir\"]", "do": null }, { "gene_id": 74052, "description": "tetratricopeptide repeat domain 21A", "gene_symbol": "[\"Ttc21a\"]", "do": null }, { "gene_id": 74053, "description": "glutamate receptor interacting protein 1", "gene_symbol": "[\"Grip1\"]", "do": "[{\"label\":\"Fraser syndrome\",\"id\":\"DOID:0090001\"},{\"label\":\"clubfoot\",\"id\":\"DOID:11836\"},{\"label\":\"recessive dystrophic epidermolysis bullosa\",\"id\":\"DOID:0060642\"}]" }, { "gene_id": 74054, "description": "Siglec family like 2", "gene_symbol": "[\"Siglecl2\"]", "do": null }, { "gene_id": 74055, "description": "phospholipase C, epsilon 1", "gene_symbol": "[\"Plce1\"]", "do": null }, { "gene_id": 74069, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 3A", "gene_symbol": "[\"Serpina3a\"]", "do": null }, { "gene_id": 74081, "description": "centrosomal protein 350", "gene_symbol": "[\"Cep350\"]", "do": null }, { "gene_id": 74102, "description": "solute carrier family 35, member A5", "gene_symbol": "[\"Slc35a5\"]", "do": null }, { "gene_id": 74103, "description": "nebulette", "gene_symbol": "[\"Nebl\"]", "do": null }, { "gene_id": 74106, "description": "DDB1 and CUL4 associated factor 6", "gene_symbol": "[\"Dcaf6\"]", "do": null }, { "gene_id": 74112, "description": "ubiquitin specific peptidase 16", "gene_symbol": "[\"Usp16\"]", "do": null }, { "gene_id": 74116, "description": "peptidase inhibitor 16", "gene_symbol": "[\"Pi16\"]", "do": null }, { "gene_id": 74136, "description": "SEC14-like lipid binding 1", "gene_symbol": "[\"Sec14l1\"]", "do": null }, { "gene_id": 74140, "description": "transmembrane 9 superfamily member 1", "gene_symbol": "[\"Tm9sf1\"]", "do": null }, { "gene_id": 74142, "description": "lon peptidase 1, mitochondrial", "gene_symbol": "[\"Lonp1\"]", "do": null }, { "gene_id": 74144, "description": "roundabout guidance receptor 4", "gene_symbol": "[\"Robo4\"]", "do": null }, { "gene_id": 74145, "description": "coagulation factor XIII, A1 subunit", "gene_symbol": "[\"F13a1\"]", "do": "[{\"label\":\"factor XIII deficiency\",\"id\":\"DOID:2211\"}]" }, { "gene_id": 74152, "description": "STRA6-like", "gene_symbol": "[\"Stra6l\"]", "do": null }, { "gene_id": 74154, "description": "unkempt family like zinc finger", "gene_symbol": "[\"Unkl\"]", "do": null }, { "gene_id": 74155, "description": "ERBB receptor feedback inhibitor 1", "gene_symbol": "[\"Errfi1\"]", "do": "[{\"label\":\"endometrial cancer\",\"id\":\"DOID:1380\"},{\"label\":\"osteoarthritis\",\"id\":\"DOID:8398\"}]" }, { "gene_id": 74157, "description": "cap methyltransferase 1", "gene_symbol": "[\"Cmtr1\"]", "do": null }, { "gene_id": 74159, "description": "acyl-Coenzyme A binding domain containing 5", "gene_symbol": "[\"Acbd5\"]", "do": "[{\"label\":\"peroxisomal disease\",\"id\":\"DOID:906\"}]" }, { "gene_id": 74174, "description": "gametocyte specific factor 1", "gene_symbol": "[\"Gtsf1\"]", "do": null }, { "gene_id": 74178, "description": "serine/threonine kinase 40", "gene_symbol": "[\"Stk40\"]", "do": null }, { "gene_id": 74180, "description": "mucin 5, subtype B, tracheobronchial", "gene_symbol": "[\"Muc5b\"]", "do": null }, { "gene_id": 74183, "description": "PPARGC1 and ESRR induced regulator, muscle 1", "gene_symbol": "[\"Perm1\"]", "do": null }, { "gene_id": 74185, "description": "1,4-alpha-glucan branching enzyme 1", "gene_symbol": "[\"Gbe1\"]", "do": "[{\"label\":\"glycogen storage disease IV\",\"id\":\"DOID:2750\"}]" }, { "gene_id": 74186, "description": "coiled-coil domain containing 3", "gene_symbol": "[\"Ccdc3\"]", "do": null }, { "gene_id": 74188, "description": "prolactin family 8, subfamily a, member 81", "gene_symbol": "[\"Prl8a8\"]", "do": null }, { "gene_id": 74191, "description": "purinergic receptor P2Y, G-protein coupled 13", "gene_symbol": "[\"P2ry13\"]", "do": null }, { "gene_id": 74199, "description": "vitrin", "gene_symbol": "[\"Vit\"]", "do": null }, { "gene_id": 74201, "description": "centrosomal protein 97", "gene_symbol": "[\"Cep97\"]", "do": null }, { "gene_id": 74203, "description": "eukaryotic translation initiation factor 4E nuclear import factor 1", "gene_symbol": "[\"Eif4enif1\"]", "do": null }, { "gene_id": 74205, "description": "acyl-CoA synthetase long-chain family member 3", "gene_symbol": "[\"Acsl3\"]", "do": null }, { "gene_id": 74206, "description": "signal-induced proliferation-associated 1 like 3", "gene_symbol": "[\"Sipa1l3\"]", "do": null }, { "gene_id": 74211, "description": "PRMT2 interacting protein", "gene_symbol": "[\"Prmt2ip\"]", "do": null }, { "gene_id": 74213, "description": "RNA binding motif protein 26", "gene_symbol": "[\"Rbm26\"]", "do": null }, { "gene_id": 74239, "description": "IQ motif containing E", "gene_symbol": "[\"Iqce\"]", "do": null }, { "gene_id": 74241, "description": "chondroitin polymerizing factor", "gene_symbol": "[\"Chpf\"]", "do": null }, { "gene_id": 74244, "description": "autophagy related 7", "gene_symbol": "[\"Atg7\"]", "do": "[{\"label\":\"Parkinson's disease\",\"id\":\"DOID:14330\"},{\"label\":\"myelodysplastic syndrome\",\"id\":\"DOID:0050908\"},{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 74245, "description": "chitobiase", "gene_symbol": "[\"Ctbs\"]", "do": null }, { "gene_id": 74246, "description": "galactose-4-epimerase, UDP", "gene_symbol": "[\"Gale\"]", "do": null }, { "gene_id": 74256, "description": "CYLD lysine 63 deubiquitinase", "gene_symbol": "[\"Cyld\"]", "do": null }, { "gene_id": 74257, "description": "tetraspanin 17", "gene_symbol": "[\"Tspan17\"]", "do": null }, { "gene_id": 74287, "description": "potassium channel modulatory factor 1", "gene_symbol": "[\"Kcmf1\"]", "do": null }, { "gene_id": 74306, "description": "serine protease 46", "gene_symbol": "[\"Prss46\"]", "do": null }, { "gene_id": 74309, "description": "oxysterol binding protein 2", "gene_symbol": "[\"Osbp2\"]", "do": null }, { "gene_id": 74322, "description": "CXXC finger protein 1", "gene_symbol": "[\"Cxxc1\"]", "do": null }, { "gene_id": 74326, "description": "heterogeneous nuclear ribonucleoprotein R", "gene_symbol": "[\"Hnrnpr\"]", "do": null }, { "gene_id": 74338, "description": "solute carrier family 6 (neurotransmitter transporter), member 19", "gene_symbol": "[\"Slc6a19\"]", "do": "[{\"label\":\"Hartnup disease\",\"id\":\"DOID:1060\"}]" }, { "gene_id": 74340, "description": "S-adenosylhomocysteine hydrolase-like 2", "gene_symbol": "[\"Ahcyl2\"]", "do": null }, { "gene_id": 74342, "description": "leucine rich repeat transmembrane neuronal 1", "gene_symbol": "[\"Lrrtm1\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 74343, "description": "CREB regulated transcription coactivator 2", "gene_symbol": "[\"Crtc2\"]", "do": null }, { "gene_id": 74355, "description": "SMC hinge domain containing 1", "gene_symbol": "[\"Smchd1\"]", "do": null }, { "gene_id": 74356, "description": "microtubule associated tyrosine carboxypeptidase 1", "gene_symbol": "[\"Matcap1\"]", "do": null }, { "gene_id": 74362, "description": "sperm associated antigen 17", "gene_symbol": "[\"Spag17\"]", "do": null }, { "gene_id": 74376, "description": "myosin XVIIIb", "gene_symbol": "[\"Myo18b\"]", "do": null }, { "gene_id": 74383, "description": "ubiquitin-associated protein 2-like", "gene_symbol": "[\"Ubap2l\"]", "do": null }, { "gene_id": 74387, "description": "exosomal polycystin 1 interacting protein", "gene_symbol": "[\"Epcip\"]", "do": null }, { "gene_id": 74392, "description": "sperm antigen with calponin homology and coiled-coil domains 1-like", "gene_symbol": "[\"Specc1l\"]", "do": "[{\"label\":\"Teebi hypertelorism syndrome 1\",\"id\":\"DOID:0080698\"},{\"label\":\"cleft palate\",\"id\":\"DOID:674\"}]" }, { "gene_id": 74393, "description": "microtubule-associated protein 10", "gene_symbol": "[\"Map10\"]", "do": null }, { "gene_id": 74409, "description": "hyaluronoglucosaminidase 6", "gene_symbol": "[\"Hyal6\"]", "do": null }, { "gene_id": 74440, "description": "c-Maf inducing protein", "gene_symbol": "[\"Cmip\"]", "do": null }, { "gene_id": 74441, "description": "solute carrier organic anion transporter family, member 6c1", "gene_symbol": "[\"Slco6c1\"]", "do": null }, { "gene_id": 74443, "description": "prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum)", "gene_symbol": "[\"P4htm\"]", "do": null }, { "gene_id": 74468, "description": "hyaluronoglucosaminidase 5", "gene_symbol": "[\"Hyal5\"]", "do": null }, { "gene_id": 74472, "description": "sperm tail PG rich repeat containing 3", "gene_symbol": "[\"Stpg3\"]", "do": null }, { "gene_id": 74477, "description": "RIKEN cDNA 4933427D14 gene", "gene_symbol": "[\"4933427D14Rik\"]", "do": null }, { "gene_id": 74480, "description": "sterile alpha motif domain containing 4", "gene_symbol": "[\"Samd4\"]", "do": null }, { "gene_id": 74486, "description": "oxysterol binding protein-like 10", "gene_symbol": "[\"Osbpl10\"]", "do": null }, { "gene_id": 74488, "description": "leucine rich repeat containing 15", "gene_symbol": "[\"Lrrc15\"]", "do": null }, { "gene_id": 74493, "description": "tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2", "gene_symbol": "[\"Tnks2\"]", "do": null }, { "gene_id": 74499, "description": "sclerostin", "gene_symbol": "[\"Sost\"]", "do": "[{\"label\":\"SOST-related sclerosing bone dysplasia\",\"id\":\"DOID:0080036\"},{\"label\":\"sclerosteosis 1\",\"id\":\"DOID:0060756\"}]" }, { "gene_id": 74513, "description": "neuropilin (NRP) and tolloid (TLL)-like 2", "gene_symbol": "[\"Neto2\"]", "do": null }, { "gene_id": 74522, "description": "microrchidia 2A", "gene_symbol": "[\"Morc2a\"]", "do": null }, { "gene_id": 74525, "description": "family with sequence similarity 234, member B", "gene_symbol": "[\"Fam234b\"]", "do": null }, { "gene_id": 74551, "description": "phosphoenolpyruvate carboxykinase 2 (mitochondrial)", "gene_symbol": "[\"Pck2\"]", "do": null }, { "gene_id": 74568, "description": "mixed lineage kinase domain-like", "gene_symbol": "[\"Mlkl\"]", "do": null }, { "gene_id": 74569, "description": "tetratricopeptide repeat domain 17", "gene_symbol": "[\"Ttc17\"]", "do": null }, { "gene_id": 74574, "description": "laeverin", "gene_symbol": "[\"Lvrn\"]", "do": null }, { "gene_id": 74577, "description": "galactosidase, beta 1-like", "gene_symbol": "[\"Glb1l\"]", "do": null }, { "gene_id": 74591, "description": "ATP-binding cassette, sub-family A member 12", "gene_symbol": "[\"Abca12\"]", "do": "[{\"label\":\"autosomal recessive congenital ichthyosis 4B\",\"id\":\"DOID:0060713\"}]" }, { "gene_id": 74603, "description": "CD200 receptor 3", "gene_symbol": "[\"Cd200r3\"]", "do": null }, { "gene_id": 74610, "description": "ATP-binding cassette, sub-family B member 8", "gene_symbol": "[\"Abcb8\"]", "do": null }, { "gene_id": 74616, "description": "secernin 3", "gene_symbol": "[\"Scrn3\"]", "do": null }, { "gene_id": 74617, "description": "serine carboxypeptidase 1", "gene_symbol": "[\"Scpep1\"]", "do": null }, { "gene_id": 74626, "description": "transmembrane protein 81", "gene_symbol": "[\"Tmem81\"]", "do": null }, { "gene_id": 74637, "description": "sedoheptulokinase", "gene_symbol": "[\"Shpk\"]", "do": null }, { "gene_id": 74649, "description": "carboxypeptidase A5", "gene_symbol": "[\"Cpa5\"]", "do": null }, { "gene_id": 74653, "description": "protein-O-mannose kinase", "gene_symbol": "[\"Pomk\"]", "do": "[{\"label\":\"hydrocephalus\",\"id\":\"DOID:10908\"}]" }, { "gene_id": 74675, "description": "patched domain containing 3", "gene_symbol": "[\"Ptchd3\"]", "do": null }, { "gene_id": 74720, "description": "transmembrane protein 114", "gene_symbol": "[\"Tmem114\"]", "do": null }, { "gene_id": 74741, "description": "C2 calcium-dependent domain containing 5", "gene_symbol": "[\"C2cd5\"]", "do": null }, { "gene_id": 74748, "description": "SLAM family member 8", "gene_symbol": "[\"Slamf8\"]", "do": null }, { "gene_id": 74761, "description": "matrix-remodelling associated 8", "gene_symbol": "[\"Mxra8\"]", "do": null }, { "gene_id": 74762, "description": "MAM domain containing glycosylphosphatidylinositol anchor 1", "gene_symbol": "[\"Mdga1\"]", "do": null }, { "gene_id": 74769, "description": "phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta", "gene_symbol": "[\"Pik3cb\"]", "do": null }, { "gene_id": 74772, "description": "ATPase type 13A2", "gene_symbol": "[\"Atp13a2\"]", "do": "[{\"label\":\"Kufor-Rakeb syndrome\",\"id\":\"DOID:0060556\"}]" }, { "gene_id": 74776, "description": "pyrophosphatase (inorganic) 2", "gene_symbol": "[\"Ppa2\"]", "do": null }, { "gene_id": 74777, "description": "selenoprotein N", "gene_symbol": "[\"Selenon\"]", "do": "[{\"label\":\"rigid spine muscular dystrophy 1\",\"id\":\"DOID:0110633\"}]" }, { "gene_id": 74781, "description": "WD repeat domain, phosphoinositide interacting 2", "gene_symbol": "[\"Wipi2\"]", "do": null }, { "gene_id": 74782, "description": "glycosyltransferase 8 domain containing 2", "gene_symbol": "[\"Glt8d2\"]", "do": null }, { "gene_id": 74919, "description": "solute carrier family 35, member F6", "gene_symbol": "[\"Slc35f6\"]", "do": null }, { "gene_id": 74987, "description": "claudin 34D", "gene_symbol": "[\"Cldn34d\"]", "do": null }, { "gene_id": 74996, "description": "ubiquitin specific peptidase 47", "gene_symbol": "[\"Usp47\"]", "do": null }, { "gene_id": 74998, "description": "RAB11 family interacting protein 2 (class I)", "gene_symbol": "[\"Rab11fip2\"]", "do": null }, { "gene_id": 75002, "description": "transmembrane (C-terminal) protease, serine 12", "gene_symbol": "[\"Tmprss12\"]", "do": null }, { "gene_id": 75019, "description": "ribonuclease, RNase A family, 10 (non-active)", "gene_symbol": "[\"Rnase10\"]", "do": null }, { "gene_id": 75099, "description": "LysM, putative peptidoglycan-binding, domain containing 4", "gene_symbol": "[\"Lysmd4\"]", "do": null }, { "gene_id": 75137, "description": "regulation of nuclear pre-mRNA domain containing 2", "gene_symbol": "[\"Rprd2\"]", "do": null }, { "gene_id": 75146, "description": "solute carrier family 68 member 1", "gene_symbol": "[\"Slc68a1\"]", "do": null }, { "gene_id": 75202, "description": "sperm acrosome associated 6", "gene_symbol": "[\"Spaca6\"]", "do": null }, { "gene_id": 75209, "description": "synaptic vesicle glycoprotein 2c", "gene_symbol": "[\"Sv2c\"]", "do": null }, { "gene_id": 75221, "description": "dipeptidylpeptidase 3", "gene_symbol": "[\"Dpp3\"]", "do": null }, { "gene_id": 75275, "description": "transmembrane and coiled-coil domains 5B", "gene_symbol": "[\"Tmco5b\"]", "do": null }, { "gene_id": 75302, "description": "ASXL transcriptional regulator 2", "gene_symbol": "[\"Asxl2\"]", "do": null }, { "gene_id": 75345, "description": "SLAM family member 7", "gene_symbol": "[\"Slamf7\"]", "do": null }, { "gene_id": 75387, "description": "sirtuin 4", "gene_symbol": "[\"Sirt4\"]", "do": null }, { "gene_id": 75409, "description": "SLIT and NTRK-like family, member 5", "gene_symbol": "[\"Slitrk5\"]", "do": null }, { "gene_id": 75410, "description": "lysine (K)-specific methyltransferase 2B", "gene_symbol": "[\"Kmt2b\"]", "do": null }, { "gene_id": 75426, "description": "insulin-like growth factor binding protein-like 1", "gene_symbol": "[\"Igfbpl1\"]", "do": null }, { "gene_id": 75482, "description": "heat shock protein family B (small) member 9", "gene_symbol": "[\"Hspb9\"]", "do": null }, { "gene_id": 75528, "description": "testis expressed 29", "gene_symbol": "[\"Tex29\"]", "do": null }, { "gene_id": 75540, "description": "fucose-1-phosphate guanylyltransferase", "gene_symbol": "[\"Fpgt\"]", "do": null }, { "gene_id": 75547, "description": "A kinase anchor protein 13", "gene_symbol": "[\"Akap13\"]", "do": null }, { "gene_id": 75553, "description": "zinc finger CCCH type containing 14", "gene_symbol": "[\"Zc3h14\"]", "do": null }, { "gene_id": 75560, "description": "E1A binding protein p400", "gene_symbol": "[\"Ep400\"]", "do": null }, { "gene_id": 75572, "description": "acylphosphatase 2, muscle type", "gene_symbol": "[\"Acyp2\"]", "do": null }, { "gene_id": 75578, "description": "FGGY carbohydrate kinase domain containing", "gene_symbol": "[\"Fggy\"]", "do": null }, { "gene_id": 75580, "description": "zinc finger and BTB domain containing 4", "gene_symbol": "[\"Zbtb4\"]", "do": null }, { "gene_id": 75596, "description": "prolactin family 7, subfamily b, member 1", "gene_symbol": "[\"Prl7b1\"]", "do": null }, { "gene_id": 75597, "description": "NADH:ubiquinone oxidoreductase complex assembly factor 2", "gene_symbol": "[\"Ndufaf2\"]", "do": null }, { "gene_id": 75599, "description": "protocadherin 1", "gene_symbol": "[\"Pcdh1\"]", "do": null }, { "gene_id": 75607, "description": "WNK lysine deficient protein kinase 2", "gene_symbol": "[\"Wnk2\"]", "do": null }, { "gene_id": 75612, "description": "glucosamine (N-acetyl)-6-sulfatase", "gene_symbol": "[\"Gns\"]", "do": "[{\"label\":\"mucopolysaccharidosis III\",\"id\":\"DOID:12801\"}]" }, { "gene_id": 75622, "description": "sperm acrosome associated 3", "gene_symbol": "[\"Spaca3\"]", "do": null }, { "gene_id": 75669, "description": "phosphoinositide-3-kinase regulatory subunit 4", "gene_symbol": "[\"Pik3r4\"]", "do": null }, { "gene_id": 75687, "description": "RHO family interacting cell polarization regulator 1", "gene_symbol": "[\"Ripor1\"]", "do": null }, { "gene_id": 75690, "description": "V-set and immunoglobulin domain containing 10 like", "gene_symbol": "[\"Vsig10l\"]", "do": null }, { "gene_id": 75698, "description": "shieldin complex subunit 2", "gene_symbol": "[\"Shld2\"]", "do": null }, { "gene_id": 75705, "description": "eukaryotic translation initiation factor 4B", "gene_symbol": "[\"Eif4b\"]", "do": null }, { "gene_id": 75710, "description": "RNA binding motif protein 12", "gene_symbol": "[\"Rbm12\"]", "do": null }, { "gene_id": 75718, "description": "von Willebrand factor A domain containing 5B1", "gene_symbol": "[\"Vwa5b1\"]", "do": null }, { "gene_id": 75731, "description": "idnK gluconokinase homolog (E. coli)", "gene_symbol": "[\"Idnk\"]", "do": null }, { "gene_id": 75734, "description": "mitochondrial fission factor", "gene_symbol": "[\"Mff\"]", "do": null }, { "gene_id": 75750, "description": "solute carrier family 10 (sodium/bile acid cotransporter family), member 6", "gene_symbol": "[\"Slc10a6\"]", "do": null }, { "gene_id": 75751, "description": "importin 4", "gene_symbol": "[\"Ipo4\"]", "do": null }, { "gene_id": 75778, "description": "thioesterase superfamily member 4", "gene_symbol": "[\"Them4\"]", "do": null }, { "gene_id": 75786, "description": "cytoskeleton associated protein 5", "gene_symbol": "[\"Ckap5\"]", "do": null }, { "gene_id": 75805, "description": "neurolysin (metallopeptidase M3 family)", "gene_symbol": "[\"Nln\"]", "do": null }, { "gene_id": 75847, "description": "CDP-L-ribitol pyrophosphorylase A", "gene_symbol": "[\"Crppa\"]", "do": "[{\"label\":\"autosomal recessive limb-girdle muscular dystrophy type 2U\",\"id\":\"DOID:0110295\"}]" }, { "gene_id": 75859, "description": "RIKEN cDNA 4930568D16 gene", "gene_symbol": "[\"4930568D16Rik\"]", "do": null }, { "gene_id": 75863, "description": "C-type lectin domain family 4, member g", "gene_symbol": "[\"Clec4g\"]", "do": null }, { "gene_id": 75870, "description": "testicular cell adhesion molecule 1", "gene_symbol": "[\"Tcam1\"]", "do": null }, { "gene_id": 75901, "description": "decapping mRNA 1A", "gene_symbol": "[\"Dcp1a\"]", "do": null }, { "gene_id": 75905, "description": "divergent protein kinase domain 2B", "gene_symbol": "[\"Dipk2b\"]", "do": null }, { "gene_id": 75956, "description": "serine/arginine repetitive matrix 2", "gene_symbol": "[\"Srrm2\"]", "do": null }, { "gene_id": 75991, "description": "SLAIN motif family, member 2", "gene_symbol": "[\"Slain2\"]", "do": null }, { "gene_id": 76014, "description": "zinc finger CCCH-type containing 18", "gene_symbol": "[\"Zc3h18\"]", "do": null }, { "gene_id": 76022, "description": "gon-4 like", "gene_symbol": "[\"Gon4l\"]", "do": null }, { "gene_id": 76025, "description": "calcium activated nucleotidase 1", "gene_symbol": "[\"Cant1\"]", "do": "[{\"label\":\"Desbuquois dysplasia\",\"id\":\"DOID:0060462\"}]" }, { "gene_id": 76044, "description": "non-SMC condensin II complex, subunit G2", "gene_symbol": "[\"Ncapg2\"]", "do": null }, { "gene_id": 76051, "description": "glucosidase, alpha; neutral C", "gene_symbol": "[\"Ganc\"]", "do": null }, { "gene_id": 76055, "description": "O-GlcNAcase", "gene_symbol": "[\"Oga\"]", "do": null }, { "gene_id": 76089, "description": "Rap guanine nucleotide exchange factor (GEF) 2", "gene_symbol": "[\"Rapgef2\"]", "do": null }, { "gene_id": 76130, "description": "LAS1-like (S. cerevisiae)", "gene_symbol": "[\"Las1l\"]", "do": null }, { "gene_id": 76142, "description": "protein phosphatase 1, regulatory inhibitor subunit 14C", "gene_symbol": "[\"Ppp1r14c\"]", "do": "[{\"label\":\"Coronavirus infectious disease\",\"id\":\"DOID:0080599\"}]" }, { "gene_id": 76161, "description": "lysosomal-associated membrane protein family, member 5", "gene_symbol": "[\"Lamp5\"]", "do": null }, { "gene_id": 76179, "description": "ubiquitin specific peptidase 31", "gene_symbol": "[\"Usp31\"]", "do": null }, { "gene_id": 76184, "description": "ATP-binding cassette, sub-family A member 6", "gene_symbol": "[\"Abca6\"]", "do": null }, { "gene_id": 76192, "description": "abhydrolase domain containing 12", "gene_symbol": "[\"Abhd12\"]", "do": "[{\"label\":\"PHARC syndrome\",\"id\":\"DOID:0080181\"}]" }, { "gene_id": 76219, "description": "adipocyte-related X-chromosome expressed sequence 1", "gene_symbol": "[\"Arxes1\"]", "do": null }, { "gene_id": 76238, "description": "glyoxylate reductase/hydroxypyruvate reductase", "gene_symbol": "[\"Grhpr\"]", "do": "[{\"label\":\"primary hyperoxaluria type 2\",\"id\":\"DOID:0111671\"}]" }, { "gene_id": 76246, "description": "RTF1, Paf1/RNA polymerase II complex component", "gene_symbol": "[\"Rtf1\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 76252, "description": "ATPase, H+ transporting, lysosomal V0 subunit E2", "gene_symbol": "[\"Atp6v0e2\"]", "do": null }, { "gene_id": 76257, "description": "solute carrier family 38, member 3", "gene_symbol": "[\"Slc38a3\"]", "do": null }, { "gene_id": 76267, "description": "fatty acid desaturase 1", "gene_symbol": "[\"Fads1\"]", "do": null }, { "gene_id": 76281, "description": "Tax1 (human T cell leukemia virus type I) binding protein 3", "gene_symbol": "[\"Tax1bp3\"]", "do": null }, { "gene_id": 76282, "description": "glutamic pyruvic transaminase, soluble", "gene_symbol": "[\"Gpt\"]", "do": null }, { "gene_id": 76293, "description": "microfibrillar-associated protein 4", "gene_symbol": "[\"Mfap4\"]", "do": null }, { "gene_id": 76299, "description": "endoplasmic reticulum protein 44", "gene_symbol": "[\"Erp44\"]", "do": null }, { "gene_id": 76302, "description": "PEST proteolytic signal containing nuclear protein", "gene_symbol": "[\"Pcnp\"]", "do": null }, { "gene_id": 76308, "description": "RAB1B, member RAS oncogene family", "gene_symbol": "[\"Rab1b\"]", "do": null }, { "gene_id": 76376, "description": "solute carrier family 24 (sodium/potassium/calcium exchanger), member 2", "gene_symbol": "[\"Slc24a2\"]", "do": null }, { "gene_id": 76399, "description": "interleukin 31", "gene_symbol": "[\"Il31\"]", "do": null }, { "gene_id": 76407, "description": "Sad1 and UNC84 domain containing 5", "gene_symbol": "[\"Sun5\"]", "do": null }, { "gene_id": 76408, "description": "ATP-binding cassette, sub-family C member 3", "gene_symbol": "[\"Abcc3\"]", "do": null }, { "gene_id": 76415, "description": "family with sequence similarity 187, member B", "gene_symbol": "[\"Fam187b\"]", "do": null }, { "gene_id": 76438, "description": "raftlin lipid raft linker 1", "gene_symbol": "[\"Rftn1\"]", "do": null }, { "gene_id": 76441, "description": "dishevelled associated activator of morphogenesis 2", "gene_symbol": "[\"Daam2\"]", "do": null }, { "gene_id": 76448, "description": "protein phosphatase 1, regulatory subunit 18", "gene_symbol": "[\"Ppp1r18\"]", "do": null }, { "gene_id": 76453, "description": "serine protease 23", "gene_symbol": "[\"Prss23\"]", "do": null }, { "gene_id": 76457, "description": "coiled-coil domain containing 134", "gene_symbol": "[\"Ccdc134\"]", "do": null }, { "gene_id": 76459, "description": "carbonic anhydrase 12", "gene_symbol": "[\"Car12\"]", "do": null }, { "gene_id": 76464, "description": "kinetochore scaffold 1", "gene_symbol": "[\"Knl1\"]", "do": null }, { "gene_id": 76469, "description": "cardiomyopathy associated 5", "gene_symbol": "[\"Cmya5\"]", "do": null }, { "gene_id": 76477, "description": "procollagen C-endopeptidase enhancer 2", "gene_symbol": "[\"Pcolce2\"]", "do": null }, { "gene_id": 76482, "description": "regulator of MON1-CCZ1", "gene_symbol": "[\"Rmc1\"]", "do": null }, { "gene_id": 76485, "description": "glycosyltransferase 8 domain containing 1", "gene_symbol": "[\"Glt8d1\"]", "do": null }, { "gene_id": 76497, "description": "protein phosphatase 1, regulatory inhibitor subunit 11", "gene_symbol": "[\"Ppp1r11\"]", "do": null }, { "gene_id": 76499, "description": "CLIP associating protein 2", "gene_symbol": "[\"Clasp2\"]", "do": null }, { "gene_id": 76507, "description": "amine oxidase, copper-containing 1", "gene_symbol": "[\"Aoc1\"]", "do": null }, { "gene_id": 76509, "description": "placenta expressed transcript 1", "gene_symbol": "[\"Plet1\"]", "do": null }, { "gene_id": 76510, "description": "trafficking protein particle complex 9", "gene_symbol": "[\"Trappc9\"]", "do": null }, { "gene_id": 76527, "description": "interleukin 34", "gene_symbol": "[\"Il34\"]", "do": null }, { "gene_id": 76551, "description": "coiled-coil domain containing 6", "gene_symbol": "[\"Ccdc6\"]", "do": null }, { "gene_id": 76559, "description": "autophagy related 2B", "gene_symbol": "[\"Atg2b\"]", "do": null }, { "gene_id": 76560, "description": "serine protease 8 (prostasin)", "gene_symbol": "[\"Prss8\"]", "do": "[{\"label\":\"autosomal recessive congenital ichthyosis 4B\",\"id\":\"DOID:0060713\"}]" }, { "gene_id": 76574, "description": "MFSD2 lysolipid transporter A, lysophospholipid", "gene_symbol": "[\"Mfsd2a\"]", "do": null }, { "gene_id": 76582, "description": "importin 11", "gene_symbol": "[\"Ipo11\"]", "do": null }, { "gene_id": 76614, "description": "inner membrane protein, mitochondrial", "gene_symbol": "[\"Immt\"]", "do": null }, { "gene_id": 76626, "description": "musashi RNA-binding protein 2", "gene_symbol": "[\"Msi2\"]", "do": null }, { "gene_id": 76645, "description": "polycystic kidney disease 1 like 2", "gene_symbol": "[\"Pkd1l2\"]", "do": null }, { "gene_id": 76654, "description": "uridine phosphorylase 2", "gene_symbol": "[\"Upp2\"]", "do": null }, { "gene_id": 76687, "description": "signal peptidase complex subunit 3 homolog (S. cerevisiae)", "gene_symbol": "[\"Spcs3\"]", "do": null }, { "gene_id": 76701, "description": "chymotrypsin C", "gene_symbol": "[\"Ctrc\"]", "do": null }, { "gene_id": 76707, "description": "CLIP associating protein 1", "gene_symbol": "[\"Clasp1\"]", "do": null }, { "gene_id": 76718, "description": "cation channel sperm associated auxiliary subunit gamma 2", "gene_symbol": "[\"Catsperg2\"]", "do": null }, { "gene_id": 76719, "description": "KAT8 regulatory NSL complex subunit 1", "gene_symbol": "[\"Kansl1\"]", "do": "[{\"label\":\"Koolen de Vries syndrome\",\"id\":\"DOID:0050880\"}]" }, { "gene_id": 76737, "description": "cysteine-rich with EGF-like domains 2", "gene_symbol": "[\"Creld2\"]", "do": null }, { "gene_id": 76740, "description": "EFR3 homolog A", "gene_symbol": "[\"Efr3a\"]", "do": null }, { "gene_id": 76742, "description": "sorting nexin family member 27", "gene_symbol": "[\"Snx27\"]", "do": null }, { "gene_id": 76757, "description": "triadin", "gene_symbol": "[\"Trdn\"]", "do": null }, { "gene_id": 76768, "description": "alkaline phosphatase, intestinal", "gene_symbol": "[\"Alpi\"]", "do": null }, { "gene_id": 76787, "description": "protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 3", "gene_symbol": "[\"Ppfia3\"]", "do": null }, { "gene_id": 76792, "description": "SREBF pathway regulator in golgi 1", "gene_symbol": "[\"Spring1\"]", "do": null }, { "gene_id": 76795, "description": "TBC1 domain family, member 9B", "gene_symbol": "[\"Tbc1d9b\"]", "do": null }, { "gene_id": 76809, "description": "Bri3 binding protein", "gene_symbol": "[\"Bri3bp\"]", "do": null }, { "gene_id": 76824, "description": "mitochondrial fission regulator 1-like", "gene_symbol": "[\"Mtfr1l\"]", "do": null }, { "gene_id": 76846, "description": "ribosomal protein S9", "gene_symbol": "[\"Rps9\"]", "do": null }, { "gene_id": 76854, "description": "G protein-coupled estrogen receptor 1", "gene_symbol": "[\"Gper1\"]", "do": null }, { "gene_id": 76858, "description": "NLR family, pyrin domain containing 14", "gene_symbol": "[\"Nlrp14\"]", "do": null }, { "gene_id": 76884, "description": "cytoplasmic FMR1 interacting protein 2", "gene_symbol": "[\"Cyfip2\"]", "do": null }, { "gene_id": 76893, "description": "ceramide synthase 2", "gene_symbol": "[\"Cers2\"]", "do": null }, { "gene_id": 76895, "description": "BICD cargo adaptor 2", "gene_symbol": "[\"Bicd2\"]", "do": null }, { "gene_id": 76897, "description": "RALY RNA binding protein-like", "gene_symbol": "[\"Ralyl\"]", "do": null }, { "gene_id": 76898, "description": "beta-1,3-glucuronyltransferase 1", "gene_symbol": "[\"B3gat1\"]", "do": null }, { "gene_id": 76905, "description": "leucine-rich alpha-2-glycoprotein 1", "gene_symbol": "[\"Lrg1\"]", "do": null }, { "gene_id": 76942, "description": "Ly6/Plaur domain containing 5", "gene_symbol": "[\"Lypd5\"]", "do": null }, { "gene_id": 76943, "description": "prosaposin-like 1", "gene_symbol": "[\"Psapl1\"]", "do": null }, { "gene_id": 76952, "description": "5'-nucleotidase, cytosolic II", "gene_symbol": "[\"Nt5c2\"]", "do": null }, { "gene_id": 76954, "description": "DENN domain containing 2B", "gene_symbol": "[\"Dennd2b\"]", "do": null }, { "gene_id": 76960, "description": "brain enriched myelin associated protein 1", "gene_symbol": "[\"Bcas1\"]", "do": null }, { "gene_id": 76965, "description": "SLIT and NTRK-like family, member 1", "gene_symbol": "[\"Slitrk1\"]", "do": "[{\"label\":\"Gilles de la Tourette syndrome\",\"id\":\"DOID:11119\"}]" }, { "gene_id": 76969, "description": "carbohydrate sulfotransferase 1", "gene_symbol": "[\"Chst1\"]", "do": null }, { "gene_id": 76976, "description": "adipocyte-related X-chromosome expressed sequence 2", "gene_symbol": "[\"Arxes2\"]", "do": null }, { "gene_id": 77034, "description": "RIKEN cDNA 2510039O18 gene", "gene_symbol": "[\"2510039O18Rik\"]", "do": null }, { "gene_id": 77038, "description": "ARF GTPase activating protein 2", "gene_symbol": "[\"Arfgap2\"]", "do": null }, { "gene_id": 77041, "description": "arylsulfatase K", "gene_symbol": "[\"Arsk\"]", "do": "[{\"label\":\"mucopolysaccharidosis\",\"id\":\"DOID:12798\"}]" }, { "gene_id": 77042, "description": "hyaluronoglucosaminidase 4", "gene_symbol": "[\"Hyal4\"]", "do": null }, { "gene_id": 77044, "description": "AT-rich interaction domain 2", "gene_symbol": "[\"Arid2\"]", "do": null }, { "gene_id": 77053, "description": "Sad1 and UNC84 domain containing 1", "gene_symbol": "[\"Sun1\"]", "do": null }, { "gene_id": 77057, "description": "stonin 1", "gene_symbol": "[\"Ston1\"]", "do": null }, { "gene_id": 77087, "description": "ankyrin repeat domain 11", "gene_symbol": "[\"Ankrd11\"]", "do": "[{\"label\":\"KBG syndrome\",\"id\":\"DOID:14780\"}]" }, { "gene_id": 77097, "description": "tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2", "gene_symbol": "[\"Tanc2\"]", "do": null }, { "gene_id": 77106, "description": "transmembrane protein 181A", "gene_symbol": "[\"Tmem181a\"]", "do": null }, { "gene_id": 77134, "description": "heterogeneous nuclear ribonucleoprotein A0", "gene_symbol": "[\"Hnrnpa0\"]", "do": null }, { "gene_id": 77219, "description": "prostaglandin reductase 2", "gene_symbol": "[\"Ptgr2\"]", "do": null }, { "gene_id": 77220, "description": "transmembrane protein 200A", "gene_symbol": "[\"Tmem200a\"]", "do": null }, { "gene_id": 77254, "description": "Yip1 interacting factor homolog B (S. cerevisiae)", "gene_symbol": "[\"Yif1b\"]", "do": null }, { "gene_id": 77300, "description": "Ras association (RalGDS/AF-6) and pleckstrin homology domains 1", "gene_symbol": "[\"Raph1\"]", "do": null }, { "gene_id": 77371, "description": "SEC24 homolog A, COPII coat complex component", "gene_symbol": "[\"Sec24a\"]", "do": null }, { "gene_id": 77397, "description": "lysozyme 3", "gene_symbol": "[\"Lyz3\"]", "do": null }, { "gene_id": 77424, "description": "serine protease inhibitor, Kazal type-like", "gene_symbol": "[\"Spinkl\"]", "do": null }, { "gene_id": 77446, "description": "heart development protein with EGF-like domains 1", "gene_symbol": "[\"Heg1\"]", "do": null }, { "gene_id": 77522, "description": "transmembrane protein 213", "gene_symbol": "[\"Tmem213\"]", "do": null }, { "gene_id": 77531, "description": "ankyrin repeat and sterile alpha motif domain containing 1B", "gene_symbol": "[\"Anks1b\"]", "do": null }, { "gene_id": 77569, "description": "LIM and calponin homology domains 1", "gene_symbol": "[\"Limch1\"]", "do": null }, { "gene_id": 77574, "description": "TRPM8 channel-associated factor 1", "gene_symbol": "[\"Tcaf1\"]", "do": null }, { "gene_id": 77578, "description": "B cell CLL/lymphoma 9", "gene_symbol": "[\"Bcl9\"]", "do": null }, { "gene_id": 77579, "description": "myosin, heavy polypeptide 10, non-muscle", "gene_symbol": "[\"Myh10\"]", "do": null }, { "gene_id": 77582, "description": "membrane bound O-acyltransferase domain containing 7", "gene_symbol": "[\"Mboat7\"]", "do": "[{\"label\":\"hydrocephalus\",\"id\":\"DOID:10908\"}]" }, { "gene_id": 77583, "description": "notum palmitoleoyl-protein carboxylesterase", "gene_symbol": "[\"Notum\"]", "do": null }, { "gene_id": 77590, "description": "carbohydrate sulfotransferase 15", "gene_symbol": "[\"Chst15\"]", "do": null }, { "gene_id": 77593, "description": "ubiquitin specific petidase 45", "gene_symbol": "[\"Usp45\"]", "do": "[{\"label\":\"Leber congenital amaurosis 19\",\"id\":\"DOID:0081169\"}]" }, { "gene_id": 77595, "description": "nucleoporin 210-like", "gene_symbol": "[\"Nup210l\"]", "do": null }, { "gene_id": 77596, "description": "adhesion G protein-coupled receptor F1", "gene_symbol": "[\"Adgrf1\"]", "do": null }, { "gene_id": 77683, "description": "euchromatic histone methyltransferase 1", "gene_symbol": "[\"Ehmt1\"]", "do": "[{\"label\":\"Kleefstra syndrome 1\",\"id\":\"DOID:0060352\"}]" }, { "gene_id": 77701, "description": "lipocalin 12", "gene_symbol": "[\"Lcn12\"]", "do": null }, { "gene_id": 77704, "description": "lipocalin 9", "gene_symbol": "[\"Lcn9\"]", "do": null }, { "gene_id": 77706, "description": "ATP-binding cassette, sub-family B member 5", "gene_symbol": "[\"Abcb5\"]", "do": null }, { "gene_id": 77727, "description": "RIKEN cDNA 6030468B19 gene", "gene_symbol": "[\"6030468B19Rik\"]", "do": null }, { "gene_id": 77739, "description": "ADAMTS-like 1", "gene_symbol": "[\"Adamtsl1\"]", "do": null }, { "gene_id": 77744, "description": "bora, aurora kinase A activator", "gene_symbol": "[\"Bora\"]", "do": null }, { "gene_id": 77767, "description": "ermin, ERM-like protein", "gene_symbol": "[\"Ermn\"]", "do": null }, { "gene_id": 77772, "description": "DC-STAMP domain containing 1", "gene_symbol": "[\"Dcst1\"]", "do": null }, { "gene_id": 77794, "description": "ADAMTS-like 2", "gene_symbol": "[\"Adamtsl2\"]", "do": "[{\"label\":\"geleophysic dysplasia 1\",\"id\":\"DOID:0111725\"},{\"label\":\"impotence\",\"id\":\"DOID:1875\"}]" }, { "gene_id": 77827, "description": "KRAB domain containing 3", "gene_symbol": "[\"Krabd3\"]", "do": null }, { "gene_id": 77908, "description": "prostate and testis expressed 13", "gene_symbol": "[\"Pate13\"]", "do": null }, { "gene_id": 77980, "description": "SET binding factor 1", "gene_symbol": "[\"Sbf1\"]", "do": "[{\"label\":\"Charcot-Marie-Tooth disease type 4B3\",\"id\":\"DOID:0110194\"}]" }, { "gene_id": 78070, "description": "carnitine palmitoyltransferase 1c", "gene_symbol": "[\"Cpt1c\"]", "do": null }, { "gene_id": 78076, "description": "lipocalin 8", "gene_symbol": "[\"Lcn8\"]", "do": null }, { "gene_id": 78134, "description": "lysophosphatidic acid receptor 4", "gene_symbol": "[\"Lpar4\"]", "do": null }, { "gene_id": 78239, "description": "serine protease inhibitor, Kunitz type 4", "gene_symbol": "[\"Spint4\"]", "do": null }, { "gene_id": 78240, "description": "cystatin 11", "gene_symbol": "[\"Cst11\"]", "do": null }, { "gene_id": 78249, "description": "adhesion G protein-coupled receptor F4", "gene_symbol": "[\"Adgrf4\"]", "do": null }, { "gene_id": 78252, "description": "neurexophilin and PC-esterase domain family, member 2", "gene_symbol": "[\"Nxpe2\"]", "do": null }, { "gene_id": 78283, "description": "MAP7 domain containing 2", "gene_symbol": "[\"Map7d2\"]", "do": null }, { "gene_id": 78284, "description": "cAMP responsive element binding protein 3-like 4", "gene_symbol": "[\"Creb3l4\"]", "do": null }, { "gene_id": 78303, "description": "H2B clustered histone 27", "gene_symbol": "[\"H2bc27\"]", "do": null }, { "gene_id": 78308, "description": "G protein-coupled receptor 108", "gene_symbol": "[\"Gpr108\"]", "do": null }, { "gene_id": 78309, "description": "cullin 9", "gene_symbol": "[\"Cul9\"]", "do": null }, { "gene_id": 78317, "description": "coiled-coil domain containing 88B", "gene_symbol": "[\"Ccdc88b\"]", "do": null }, { "gene_id": 78339, "description": "tweety family member 3", "gene_symbol": "[\"Ttyh3\"]", "do": null }, { "gene_id": 78354, "description": "LY6/PLAUR domain containing 8 like", "gene_symbol": "[\"Lypd8l\"]", "do": null }, { "gene_id": 78369, "description": "intercellular adhesion molecule 4, Landsteiner-Wiener blood group", "gene_symbol": "[\"Icam4\"]", "do": null }, { "gene_id": 78388, "description": "major vault protein", "gene_symbol": "[\"Mvp\"]", "do": null }, { "gene_id": 78405, "description": "neurotrophin 5", "gene_symbol": "[\"Ntf5\"]", "do": null }, { "gene_id": 78416, "description": "ribonuclease, RNase A family, 6", "gene_symbol": "[\"Rnase6\"]", "do": null }, { "gene_id": 78455, "description": "helicase with zinc finger domain", "gene_symbol": "[\"Helz\"]", "do": null }, { "gene_id": 78560, "description": "adhesion G protein-coupled receptor A2", "gene_symbol": "[\"Adgra2\"]", "do": null }, { "gene_id": 78618, "description": "ArfGAP with coiled-coil, ankyrin repeat and PH domains 2", "gene_symbol": "[\"Acap2\"]", "do": null }, { "gene_id": 78634, "description": "sperm acrosome associated 7", "gene_symbol": "[\"Spaca7\"]", "do": null }, { "gene_id": 78653, "description": "bolA family member 3", "gene_symbol": "[\"Bola3\"]", "do": null }, { "gene_id": 78655, "description": "eukaryotic translation initiation factor 3, subunit J1", "gene_symbol": "[\"Eif3j1\"]", "do": null }, { "gene_id": 78656, "description": "bromodomain containing 8", "gene_symbol": "[\"Brd8\"]", "do": null }, { "gene_id": 78658, "description": "non-SMC condensin II complex, subunit D3", "gene_symbol": "[\"Ncapd3\"]", "do": null }, { "gene_id": 78749, "description": "filamin A interacting protein 1-like", "gene_symbol": "[\"Filip1l\"]", "do": null }, { "gene_id": 78752, "description": "chondroitin sulfate N-acetylgalactosaminyltransferase 2", "gene_symbol": "[\"Csgalnact2\"]", "do": null }, { "gene_id": 78753, "description": "lipase family member M", "gene_symbol": "[\"Lipm\"]", "do": null }, { "gene_id": 78754, "description": "polypeptide N-acetylgalactosaminyltransferase 15", "gene_symbol": "[\"Galnt15\"]", "do": null }, { "gene_id": 78772, "description": "hedgehog interacting protein-like 2", "gene_symbol": "[\"Hhipl2\"]", "do": null }, { "gene_id": 78779, "description": "spermatogenesis associated 2-like", "gene_symbol": "[\"Spata2l\"]", "do": null }, { "gene_id": 78781, "description": "zinc finger CCCH type, antiviral 1", "gene_symbol": "[\"Zc3hav1\"]", "do": null }, { "gene_id": 78789, "description": "V-set and immunoglobulin domain containing 1", "gene_symbol": "[\"Vsig1\"]", "do": null }, { "gene_id": 78816, "description": "Gem-interacting protein", "gene_symbol": "[\"Gmip\"]", "do": null }, { "gene_id": 78826, "description": "purinergic receptor P2Y, G-protein coupled 10", "gene_symbol": "[\"P2ry10\"]", "do": null }, { "gene_id": 78829, "description": "Tsc22 domain family, member 4", "gene_symbol": "[\"Tsc22d4\"]", "do": null }, { "gene_id": 78832, "description": "CDK2 associated, cullin domain 1", "gene_symbol": "[\"Cacul1\"]", "do": null }, { "gene_id": 78892, "description": "cysteine-rich secretory protein LCCL domain containing 2", "gene_symbol": "[\"Crispld2\"]", "do": null }, { "gene_id": 78893, "description": "CCR4-NOT transcription complex, subunit 10", "gene_symbol": "[\"Cnot10\"]", "do": null }, { "gene_id": 78908, "description": "immunoglobulin superfamily, member 3", "gene_symbol": "[\"Igsf3\"]", "do": null }, { "gene_id": 78912, "description": "Sp2 transcription factor", "gene_symbol": "[\"Sp2\"]", "do": null }, { "gene_id": 78920, "description": "dihydrolipoamide S-succinyltransferase", "gene_symbol": "[\"Dlst\"]", "do": null }, { "gene_id": 78923, "description": "chondroitin sulfate synthase 3", "gene_symbol": "[\"Chsy3\"]", "do": null }, { "gene_id": 78926, "description": "growth arrest-specific 2 like 1", "gene_symbol": "[\"Gas2l1\"]", "do": null }, { "gene_id": 78928, "description": "phosphatidylinositol glycan anchor biosynthesis, class T", "gene_symbol": "[\"Pigt\"]", "do": null }, { "gene_id": 78937, "description": "AVL9 cell migration associated", "gene_symbol": "[\"Avl9\"]", "do": null }, { "gene_id": 78943, "description": "endoplasmic reticulum to nucleus signalling 1", "gene_symbol": "[\"Ern1\"]", "do": null }, { "gene_id": 78977, "description": "popeye domain containing 3", "gene_symbol": "[\"Popdc3\"]", "do": null }, { "gene_id": 79201, "description": "tumor necrosis factor receptor superfamily, member 23", "gene_symbol": "[\"Tnfrsf23\"]", "do": null }, { "gene_id": 79202, "description": "tumor necrosis factor receptor superfamily, member 22", "gene_symbol": "[\"Tnfrsf22\"]", "do": null }, { "gene_id": 80281, "description": "CTTNBP2 N-terminal like", "gene_symbol": "[\"Cttnbp2nl\"]", "do": null }, { "gene_id": 80285, "description": "poly (ADP-ribose) polymerase family, member 9", "gene_symbol": "[\"Parp9\"]", "do": null }, { "gene_id": 80286, "description": "tumor suppressor candidate 3", "gene_symbol": "[\"Tusc3\"]", "do": null }, { "gene_id": 80288, "description": "B cell CLL/lymphoma 9-like", "gene_symbol": "[\"Bcl9l\"]", "do": null }, { "gene_id": 80289, "description": "LysM, putative peptidoglycan-binding, domain containing 3", "gene_symbol": "[\"Lysmd3\"]", "do": null }, { "gene_id": 80290, "description": "G protein-coupled receptor 146", "gene_symbol": "[\"Gpr146\"]", "do": null }, { "gene_id": 80294, "description": "protein O-fucosyltransferase 2", "gene_symbol": "[\"Pofut2\"]", "do": null }, { "gene_id": 80721, "description": "solute carrier family 19, member 3", "gene_symbol": "[\"Slc19a3\"]", "do": "[{\"label\":\"biotin-responsive basal ganglia disease\",\"id\":\"DOID:0050659\"}]" }, { "gene_id": 80733, "description": "carbonic anhydrase 15", "gene_symbol": "[\"Car15\"]", "do": null }, { "gene_id": 80749, "description": "leucine rich repeat and fibronectin type III domain containing 1", "gene_symbol": "[\"Lrfn1\"]", "do": null }, { "gene_id": 80751, "description": "ring finger protein 34", "gene_symbol": "[\"Rnf34\"]", "do": null }, { "gene_id": 80752, "description": "FAM20C, golgi associated secretory pathway kinase", "gene_symbol": "[\"Fam20c\"]", "do": "[{\"label\":\"rickets\",\"id\":\"DOID:10609\"}]" }, { "gene_id": 80782, "description": "killer cell lectin-like receptor subfamily B member 1B", "gene_symbol": "[\"Klrb1b\"]", "do": null }, { "gene_id": 80860, "description": "GH3 domain containing", "gene_symbol": "[\"Ghdc\"]", "do": null }, { "gene_id": 80861, "description": "DExH-box helicase 58", "gene_symbol": "[\"Dhx58\"]", "do": null }, { "gene_id": 80877, "description": "LPS-responsive beige-like anchor", "gene_symbol": "[\"Lrba\"]", "do": null }, { "gene_id": 80883, "description": "netrin G1", "gene_symbol": "[\"Ntng1\"]", "do": null }, { "gene_id": 80891, "description": "Fc receptor like 2", "gene_symbol": "[\"Fcrl2\"]", "do": null }, { "gene_id": 80893, "description": "transmembrane protease, serine 5 (spinesin)", "gene_symbol": "[\"Tmprss5\"]", "do": null }, { "gene_id": 80898, "description": "endoplasmic reticulum aminopeptidase 1", "gene_symbol": "[\"Erap1\"]", "do": null }, { "gene_id": 80901, "description": "C-X-C motif chemokine receptor 6", "gene_symbol": "[\"Cxcr6\"]", "do": null }, { "gene_id": 80903, "description": "fibroblast growth factor 16", "gene_symbol": "[\"Fgf16\"]", "do": null }, { "gene_id": 80908, "description": "ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase", "gene_symbol": "[\"Abo\"]", "do": null }, { "gene_id": 80910, "description": "G protein-coupled receptor 84", "gene_symbol": "[\"Gpr84\"]", "do": null }, { "gene_id": 80912, "description": "pumilio RNA-binding family member 1", "gene_symbol": "[\"Pum1\"]", "do": null }, { "gene_id": 80913, "description": "pumilio RNA-binding family member 2", "gene_symbol": "[\"Pum2\"]", "do": null }, { "gene_id": 80978, "description": "MAS-related GPR, member H", "gene_symbol": "[\"Mrgprh\"]", "do": null }, { "gene_id": 80979, "description": "solute carrier family 26, member 5", "gene_symbol": "[\"Slc26a5\"]", "do": null }, { "gene_id": 80982, "description": "cell migration inducing protein, hyaluronan binding", "gene_symbol": "[\"Cemip\"]", "do": null }, { "gene_id": 80986, "description": "cytoskeleton associated protein 2", "gene_symbol": "[\"Ckap2\"]", "do": null }, { "gene_id": 80987, "description": "NCK interacting protein with SH3 domain", "gene_symbol": "[\"Nckipsd\"]", "do": null }, { "gene_id": 81000, "description": "RAD54 like 2 (S. cerevisiae)", "gene_symbol": "[\"Rad54l2\"]", "do": null }, { "gene_id": 81006, "description": "G protein-coupled receptor 63", "gene_symbol": "[\"Gpr63\"]", "do": null }, { "gene_id": 81500, "description": "SIL1 nucleotide exchange factor", "gene_symbol": "[\"Sil1\"]", "do": null }, { "gene_id": 81600, "description": "chitinase, acidic 1", "gene_symbol": "[\"Chia1\"]", "do": null }, { "gene_id": 81701, "description": "EGF-like domain 8", "gene_symbol": "[\"Egfl8\"]", "do": null }, { "gene_id": 81702, "description": "ankyrin repeat domain 17", "gene_symbol": "[\"Ankrd17\"]", "do": null }, { "gene_id": 81799, "description": "C1q and tumor necrosis factor related protein 3", "gene_symbol": "[\"C1qtnf3\"]", "do": null }, { "gene_id": 81840, "description": "sortilin-related VPS10 domain containing receptor 2", "gene_symbol": "[\"Sorcs2\"]", "do": null }, { "gene_id": 81877, "description": "tenascin XB", "gene_symbol": "[\"Tnxb\"]", "do": null }, { "gene_id": 81897, "description": "toll-like receptor 9", "gene_symbol": "[\"Tlr9\"]", "do": null }, { "gene_id": 81905, "description": "calcium channel, voltage-dependent, gamma subunit 8", "gene_symbol": "[\"Cacng8\"]", "do": null }, { "gene_id": 81910, "description": "ribosome binding protein 1", "gene_symbol": "[\"Rrbp1\"]", "do": null }, { "gene_id": 83379, "description": "klotho beta", "gene_symbol": "[\"Klb\"]", "do": null }, { "gene_id": 83382, "description": "sialic acid binding Ig-like lectin E", "gene_symbol": "[\"Siglece\"]", "do": null }, { "gene_id": 83395, "description": "trans-acting transcription factor 6", "gene_symbol": "[\"Sp6\"]", "do": null }, { "gene_id": 83397, "description": "A kinase anchor protein 12", "gene_symbol": "[\"Akap12\"]", "do": null }, { "gene_id": 83398, "description": "N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3", "gene_symbol": "[\"Ndst3\"]", "do": null }, { "gene_id": 83429, "description": "cystinosis, nephropathic", "gene_symbol": "[\"Ctns\"]", "do": "[{\"label\":\"cystinosis\",\"id\":\"DOID:1064\"}]" }, { "gene_id": 83433, "description": "triggering receptor expressed on myeloid cells 2", "gene_symbol": "[\"Trem2\"]", "do": "[{\"label\":\"frontotemporal dementia\",\"id\":\"DOID:9255\"}]" }, { "gene_id": 83453, "description": "chordin-like 1", "gene_symbol": "[\"Chrdl1\"]", "do": null }, { "gene_id": 83485, "description": "neugrin, neurite outgrowth associated", "gene_symbol": "[\"Ngrn\"]", "do": null }, { "gene_id": 83554, "description": "follistatin-like 3", "gene_symbol": "[\"Fstl3\"]", "do": null }, { "gene_id": 83563, "description": "ubiquitin specific peptidase 26", "gene_symbol": "[\"Usp26\"]", "do": null }, { "gene_id": 83603, "description": "ELOVL fatty acid elongase 4", "gene_symbol": "[\"Elovl4\"]", "do": "[{\"label\":\"Stargardt disease\",\"id\":\"DOID:0050817\"}]" }, { "gene_id": 83674, "description": "cyclin M1", "gene_symbol": "[\"Cnnm1\"]", "do": null }, { "gene_id": 83704, "description": "solute carrier family 12 (potassium/chloride transporters), member 9", "gene_symbol": "[\"Slc12a9\"]", "do": null }, { "gene_id": 83767, "description": "WASP family, member 1", "gene_symbol": "[\"Wasf1\"]", "do": null }, { "gene_id": 83768, "description": "dipeptidylpeptidase 7", "gene_symbol": "[\"Dpp7\"]", "do": null }, { "gene_id": 83770, "description": "taste receptor, type 1, member 2", "gene_symbol": "[\"Tas1r2\"]", "do": null }, { "gene_id": 83771, "description": "taste receptor, type 1, member 3", "gene_symbol": "[\"Tas1r3\"]", "do": null }, { "gene_id": 83796, "description": "SWI/SNF related BAF chromatin remodeling complex subunit D2", "gene_symbol": "[\"Smarcd2\"]", "do": null }, { "gene_id": 83797, "description": "SWI/SNF related BAF chromatin remodeling complex subunit D1", "gene_symbol": "[\"Smarcd1\"]", "do": null }, { "gene_id": 83921, "description": "cell migration inducing hyaluronidase 2", "gene_symbol": "[\"Cemip2\"]", "do": null }, { "gene_id": 83924, "description": "G protein-coupled receptor 137B", "gene_symbol": "[\"Gpr137b\"]", "do": null }, { "gene_id": 83961, "description": "neuregulin 4", "gene_symbol": "[\"Nrg4\"]", "do": null }, { "gene_id": 83964, "description": "junction adhesion molecule 3", "gene_symbol": "[\"Jam3\"]", "do": null }, { "gene_id": 83965, "description": "ectonucleotide pyrophosphatase/phosphodiesterase 5", "gene_symbol": "[\"Enpp5\"]", "do": null }, { "gene_id": 83995, "description": "matrix metallopeptidase 1a (interstitial collagenase)", "gene_symbol": "[\"Mmp1a\"]", "do": null }, { "gene_id": 83997, "description": "sarcolemma associated protein", "gene_symbol": "[\"Slmap\"]", "do": null }, { "gene_id": 84004, "description": "melanoma cell adhesion molecule", "gene_symbol": "[\"Mcam\"]", "do": null }, { "gene_id": 84035, "description": "kringle containing transmembrane protein 1", "gene_symbol": "[\"Kremen1\"]", "do": null }, { "gene_id": 84092, "description": "ubiquitin specific peptidase 8", "gene_symbol": "[\"Usp8\"]", "do": null }, { "gene_id": 84094, "description": "plasmalemma vesicle associated protein", "gene_symbol": "[\"Plvap\"]", "do": null }, { "gene_id": 84111, "description": "G protein-coupled receptor 87", "gene_symbol": "[\"Gpr87\"]", "do": null }, { "gene_id": 84112, "description": "succinate receptor 1", "gene_symbol": "[\"Sucnr1\"]", "do": null }, { "gene_id": 84544, "description": "CD96 antigen", "gene_symbol": "[\"Cd96\"]", "do": null }, { "gene_id": 84585, "description": "ring finger protein 123", "gene_symbol": "[\"Rnf123\"]", "do": null }, { "gene_id": 84652, "description": "hyccin PI4KA lipid kinase complex subunit 1", "gene_symbol": "[\"Hycc1\"]", "do": null }, { "gene_id": 85031, "description": "phospholipase A1 member A", "gene_symbol": "[\"Pla1a\"]", "do": null }, { "gene_id": 93671, "description": "CD163 antigen", "gene_symbol": "[\"Cd163\"]", "do": null }, { "gene_id": 93672, "description": "interleukin 24", "gene_symbol": "[\"Il24\"]", "do": null }, { "gene_id": 93675, "description": "C-type lectin domain family 2, member i", "gene_symbol": "[\"Clec2i\"]", "do": null }, { "gene_id": 93683, "description": "glucuronyl C5-epimerase", "gene_symbol": "[\"Glce\"]", "do": null }, { "gene_id": 93685, "description": "ectonucleoside triphosphate diphosphohydrolase 7", "gene_symbol": "[\"Entpd7\"]", "do": null }, { "gene_id": 93686, "description": "RNA binding protein, fox-1 homolog (C. elegans) 2", "gene_symbol": "[\"Rbfox2\"]", "do": null }, { "gene_id": 93690, "description": "G protein-coupled receptor 45", "gene_symbol": "[\"Gpr45\"]", "do": null }, { "gene_id": 93694, "description": "C-type lectin domain family 2, member d", "gene_symbol": "[\"Clec2d\"]", "do": null }, { "gene_id": 93695, "description": "glycoprotein (transmembrane) nmb", "gene_symbol": "[\"Gpnmb\"]", "do": "[{\"label\":\"pigment dispersion syndrome\",\"id\":\"DOID:0060680\"}]" }, { "gene_id": 93699, "description": "protocadherin gamma subfamily B, 1", "gene_symbol": "[\"Pcdhgb1\"]", "do": null }, { "gene_id": 93700, "description": "protocadherin gamma subfamily B, 2", "gene_symbol": "[\"Pcdhgb2\"]", "do": null }, { "gene_id": 93701, "description": "protocadherin gamma subfamily B, 4", "gene_symbol": "[\"Pcdhgb4\"]", "do": null }, { "gene_id": 93702, "description": "protocadherin gamma subfamily B, 5", "gene_symbol": "[\"Pcdhgb5\"]", "do": null }, { "gene_id": 93704, "description": "protocadherin gamma subfamily B, 7", "gene_symbol": "[\"Pcdhgb7\"]", "do": null }, { "gene_id": 93706, "description": "protocadherin gamma subfamily C, 3", "gene_symbol": "[\"Pcdhgc3\"]", "do": null }, { "gene_id": 93707, "description": "protocadherin gamma subfamily C, 4", "gene_symbol": "[\"Pcdhgc4\"]", "do": null }, { "gene_id": 93708, "description": "protocadherin gamma subfamily C, 5", "gene_symbol": "[\"Pcdhgc5\"]", "do": null }, { "gene_id": 93709, "description": "protocadherin gamma subfamily A, 1", "gene_symbol": "[\"Pcdhga1\"]", "do": null }, { "gene_id": 93711, "description": "protocadherin gamma subfamily A, 3", "gene_symbol": "[\"Pcdhga3\"]", "do": null }, { "gene_id": 93712, "description": "protocadherin gamma subfamily A, 4", "gene_symbol": "[\"Pcdhga4\"]", "do": null }, { "gene_id": 93713, "description": "protocadherin gamma subfamily A, 5", "gene_symbol": "[\"Pcdhga5\"]", "do": null }, { "gene_id": 93716, "description": "protocadherin gamma subfamily A, 8", "gene_symbol": "[\"Pcdhga8\"]", "do": null }, { "gene_id": 93717, "description": "protocadherin gamma subfamily A, 9", "gene_symbol": "[\"Pcdhga9\"]", "do": null }, { "gene_id": 93721, "description": "carboxypeptidase N, polypeptide 1", "gene_symbol": "[\"Cpn1\"]", "do": null }, { "gene_id": 93732, "description": "acyl-Coenzyme A oxidase 2, branched chain", "gene_symbol": "[\"Acox2\"]", "do": null }, { "gene_id": 93735, "description": "wingless-type MMTV integration site family, member 16", "gene_symbol": "[\"Wnt16\"]", "do": null }, { "gene_id": 93736, "description": "AF4/FMR2 family, member 4", "gene_symbol": "[\"Aff4\"]", "do": null }, { "gene_id": 93737, "description": "par-6 family cell polarity regulator gamma", "gene_symbol": "[\"Pard6g\"]", "do": null }, { "gene_id": 93759, "description": "sirtuin 1", "gene_symbol": "[\"Sirt1\"]", "do": null }, { "gene_id": 93760, "description": "AT-rich interaction domain 1A", "gene_symbol": "[\"Arid1a\"]", "do": "[{\"label\":\"Coffin-Siris syndrome\",\"id\":\"DOID:1925\"}]" }, { "gene_id": 93762, "description": "SNF2 related chromatin remodeling ATPase 5", "gene_symbol": "[\"Smarca5\"]", "do": null }, { "gene_id": 93835, "description": "amnionless", "gene_symbol": "[\"Amn\"]", "do": null }, { "gene_id": 93842, "description": "immunoglobulin superfamily, member 9", "gene_symbol": "[\"Igsf9\"]", "do": null }, { "gene_id": 93871, "description": "bromodomain and WD repeat domain containing 1", "gene_symbol": "[\"Brwd1\"]", "do": null }, { "gene_id": 93877, "description": "protocadherin beta 6", "gene_symbol": "[\"Pcdhb6\"]", "do": null }, { "gene_id": 93879, "description": "protocadherin beta 8", "gene_symbol": "[\"Pcdhb8\"]", "do": null }, { "gene_id": 93885, "description": "protocadherin beta 14", "gene_symbol": "[\"Pcdhb14\"]", "do": null }, { "gene_id": 93889, "description": "protocadherin beta 18", "gene_symbol": "[\"Pcdhb18\"]", "do": null }, { "gene_id": 93896, "description": "glucagon-like peptide 2 receptor", "gene_symbol": "[\"Glp2r\"]", "do": null }, { "gene_id": 93897, "description": "frizzled class receptor 10", "gene_symbol": "[\"Fzd10\"]", "do": null }, { "gene_id": 93961, "description": "UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5", "gene_symbol": "[\"B3galt5\"]", "do": null }, { "gene_id": 94043, "description": "TM2 domain containing 1", "gene_symbol": "[\"Tm2d1\"]", "do": null }, { "gene_id": 94044, "description": "BCL2 like 13", "gene_symbol": "[\"Bcl2l13\"]", "do": null }, { "gene_id": 94045, "description": "purinergic receptor P2X, ligand-gated ion channel, 5", "gene_symbol": "[\"P2rx5\"]", "do": null }, { "gene_id": 94071, "description": "C-type lectin domain family 2, member h", "gene_symbol": "[\"Clec2h\"]", "do": null }, { "gene_id": 94089, "description": "tripartite motif-containing 7", "gene_symbol": "[\"Trim7\"]", "do": null }, { "gene_id": 94093, "description": "tripartite motif-containing 33", "gene_symbol": "[\"Trim33\"]", "do": null }, { "gene_id": 94109, "description": "CUB and Sushi multiple domains 1", "gene_symbol": "[\"Csmd1\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 94111, "description": "matrix extracellular phosphoglycoprotein with ASARM motif (bone)", "gene_symbol": "[\"Mepe\"]", "do": null }, { "gene_id": 94112, "description": "mediator complex subunit 15", "gene_symbol": "[\"Med15\"]", "do": null }, { "gene_id": 94175, "description": "histidine-rich glycoprotein", "gene_symbol": "[\"Hrg\"]", "do": null }, { "gene_id": 94176, "description": "dedicator of cyto-kinesis 2", "gene_symbol": "[\"Dock2\"]", "do": null }, { "gene_id": 94178, "description": "mucolipin 1", "gene_symbol": "[\"Mcoln1\"]", "do": "[{\"label\":\"mucolipidosis type IV\",\"id\":\"DOID:0080490\"}]" }, { "gene_id": 94181, "description": "N-acetylneuraminic acid synthase (sialic acid synthase)", "gene_symbol": "[\"Nans\"]", "do": null }, { "gene_id": 94184, "description": "pyridoxal-dependent decarboxylase domain containing 1", "gene_symbol": "[\"Pdxdc1\"]", "do": null }, { "gene_id": 94185, "description": "tumor necrosis factor receptor superfamily, member 21", "gene_symbol": "[\"Tnfrsf21\"]", "do": null }, { "gene_id": 94192, "description": "core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1", "gene_symbol": "[\"C1galt1\"]", "do": null }, { "gene_id": 94214, "description": "sparc/osteonectin, cwcv and kazal-like domains proteoglycan 2", "gene_symbol": "[\"Spock2\"]", "do": null }, { "gene_id": 94215, "description": "UDP glucuronosyltransferase 2 family, polypeptide A1", "gene_symbol": "[\"Ugt2a1\"]", "do": null }, { "gene_id": 94217, "description": "low density lipoprotein-related protein 1B", "gene_symbol": "[\"Lrp1b\"]", "do": null }, { "gene_id": 94218, "description": "cyclin M3", "gene_symbol": "[\"Cnnm3\"]", "do": null }, { "gene_id": 94219, "description": "cyclin M2", "gene_symbol": "[\"Cnnm2\"]", "do": null }, { "gene_id": 94220, "description": "cyclin M4", "gene_symbol": "[\"Cnnm4\"]", "do": null }, { "gene_id": 94226, "description": "sphingosine-1-phosphate receptor 5", "gene_symbol": "[\"S1pr5\"]", "do": null }, { "gene_id": 94227, "description": "peptidase inhibitor 15", "gene_symbol": "[\"Pi15\"]", "do": null }, { "gene_id": 94229, "description": "solute carrier family 4, sodium bicarbonate cotransporter-like, member 10", "gene_symbol": "[\"Slc4a10\"]", "do": null }, { "gene_id": 94230, "description": "cleavage and polyadenylation specific factor 1", "gene_symbol": "[\"Cpsf1\"]", "do": null }, { "gene_id": 94232, "description": "ubiquilin 4", "gene_symbol": "[\"Ubqln4\"]", "do": null }, { "gene_id": 94242, "description": "tubulointerstitial nephritis antigen-like 1", "gene_symbol": "[\"Tinagl1\"]", "do": null }, { "gene_id": 94249, "description": "solute carrier family 24 (sodium/potassium/calcium exchanger), member 3", "gene_symbol": "[\"Slc24a3\"]", "do": null }, { "gene_id": 94275, "description": "MAGE family member D1", "gene_symbol": "[\"Maged1\"]", "do": null }, { "gene_id": 94280, "description": "sideroflexin 3", "gene_symbol": "[\"Sfxn3\"]", "do": null }, { "gene_id": 94282, "description": "sideroflexin 5", "gene_symbol": "[\"Sfxn5\"]", "do": null }, { "gene_id": 94284, "description": "UDP glucuronosyltransferase 1 family, polypeptide A6A", "gene_symbol": "[\"Ugt1a6a\"]", "do": null }, { "gene_id": 94315, "description": "papillary renal cell carcinoma (translocation-associated)", "gene_symbol": "[\"Prcc\"]", "do": null }, { "gene_id": 94332, "description": "cell adhesion molecule 3", "gene_symbol": "[\"Cadm3\"]", "do": null }, { "gene_id": 94352, "description": "lysyl oxidase-like 2", "gene_symbol": "[\"Loxl2\"]", "do": null }, { "gene_id": 96875, "description": "proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein)", "gene_symbol": "[\"Prg4\"]", "do": null }, { "gene_id": 96935, "description": "sushi domain containing 4", "gene_symbol": "[\"Susd4\"]", "do": null }, { "gene_id": 96957, "description": "transmembrane protein 62", "gene_symbol": "[\"Tmem62\"]", "do": null }, { "gene_id": 96979, "description": "prostaglandin E synthase 2", "gene_symbol": "[\"Ptges2\"]", "do": null }, { "gene_id": 97064, "description": "WW domain containing transcription regulator 1", "gene_symbol": "[\"Wwtr1\"]", "do": "[{\"label\":\"nephronophthisis\",\"id\":\"DOID:12712\"}]" }, { "gene_id": 97122, "description": "H4 clustered histone 14", "gene_symbol": "[\"H4c14\"]", "do": null }, { "gene_id": 97130, "description": "NHS like 3", "gene_symbol": "[\"Nhsl3\"]", "do": null }, { "gene_id": 97212, "description": "hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha", "gene_symbol": "[\"Hadha\"]", "do": null }, { "gene_id": 97287, "description": "myotubularin related protein 14", "gene_symbol": "[\"Mtmr14\"]", "do": null }, { "gene_id": 97440, "description": "UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9", "gene_symbol": "[\"B3gnt9\"]", "do": null }, { "gene_id": 97541, "description": "glutaminyl-tRNA synthetase 1", "gene_symbol": "[\"Qars1\"]", "do": null }, { "gene_id": 97761, "description": "small G protein signaling modulator 2", "gene_symbol": "[\"Sgsm2\"]", "do": null }, { "gene_id": 97884, "description": "UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 2", "gene_symbol": "[\"B3galnt2\"]", "do": null }, { "gene_id": 98170, "description": "transmembrane protein 132A", "gene_symbol": "[\"Tmem132a\"]", "do": null }, { "gene_id": 98303, "description": "RIKEN cDNA D630023F18 gene", "gene_symbol": "[\"D630023F18Rik\"]", "do": null }, { "gene_id": 98365, "description": "SLAM family member 9", "gene_symbol": "[\"Slamf9\"]", "do": null }, { "gene_id": 98366, "description": "small ArfGAP 1", "gene_symbol": "[\"Smap1\"]", "do": null }, { "gene_id": 98376, "description": "golgin, RAB6-interacting", "gene_symbol": "[\"Gorab\"]", "do": null }, { "gene_id": 98386, "description": "lamin B receptor", "gene_symbol": "[\"Lbr\"]", "do": "[{\"label\":\"Pelger-Huet anomaly\",\"id\":\"DOID:9631\"},{\"label\":\"ichthyosis vulgaris\",\"id\":\"DOID:1702\"},{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 98388, "description": "carbohydrate sulfotransferase 10", "gene_symbol": "[\"Chst10\"]", "do": null }, { "gene_id": 98404, "description": "expressed sequence AI597479", "gene_symbol": "[\"AI597479\"]", "do": null }, { "gene_id": 98660, "description": "ATPase, Na+/K+ transporting, alpha 2 polypeptide", "gene_symbol": "[\"Atp1a2\"]", "do": "[{\"label\":\"familial hemiplegic migraine 2\",\"id\":\"DOID:0111182\"}]" }, { "gene_id": 98682, "description": "major facilitator superfamily domain containing 6", "gene_symbol": "[\"Mfsd6\"]", "do": null }, { "gene_id": 98685, "description": "tRNA methyltransferase 1 like", "gene_symbol": "[\"Trmt1l\"]", "do": null }, { "gene_id": 98732, "description": "RAB3 GTPase activating protein subunit 2", "gene_symbol": "[\"Rab3gap2\"]", "do": null }, { "gene_id": 98741, "description": "potassium voltage gated channel, Shab-related subfamily, member 2", "gene_symbol": "[\"Kcnb2\"]", "do": null }, { "gene_id": 98870, "description": "expressed sequence AI182371", "gene_symbol": "[\"AI182371\"]", "do": null }, { "gene_id": 98952, "description": "estrogen-induced osteoclastogenesis regulator 1", "gene_symbol": "[\"Eeig1\"]", "do": null }, { "gene_id": 98970, "description": "fibrinogen C domain containing 1", "gene_symbol": "[\"Fibcd1\"]", "do": null }, { "gene_id": 99003, "description": "glutamine and serine rich 1", "gene_symbol": "[\"Qser1\"]", "do": null }, { "gene_id": 99010, "description": "lysophosphatidylcholine acyltransferase 4", "gene_symbol": "[\"Lpcat4\"]", "do": null }, { "gene_id": 99011, "description": "protein-O-mannosyltransferase 1", "gene_symbol": "[\"Pomt1\"]", "do": "[{\"label\":\"muscular dystrophy-dystroglycanopathy type B1\",\"id\":\"DOID:0050588\"}]" }, { "gene_id": 99031, "description": "oxysterol binding protein-like 6", "gene_symbol": "[\"Osbpl6\"]", "do": null }, { "gene_id": 99151, "description": "cerebral endothelial cell adhesion molecule", "gene_symbol": "[\"Cercam\"]", "do": null }, { "gene_id": 99237, "description": "transmembrane 9 superfamily member 4", "gene_symbol": "[\"Tm9sf4\"]", "do": null }, { "gene_id": 99296, "description": "histamine receptor H3", "gene_symbol": "[\"Hrh3\"]", "do": null }, { "gene_id": 99326, "description": "GTPase activating RANGAP domain-like 3", "gene_symbol": "[\"Garnl3\"]", "do": null }, { "gene_id": 99375, "description": "cullin 4A", "gene_symbol": "[\"Cul4a\"]", "do": null }, { "gene_id": 99377, "description": "spalt like transcription factor 4", "gene_symbol": "[\"Sall4\"]", "do": "[{\"label\":\"Duane-radial ray syndrome\",\"id\":\"DOID:0060747\"},{\"label\":\"otitis media\",\"id\":\"DOID:10754\"}]" }, { "gene_id": 99412, "description": "golgin A2", "gene_symbol": "[\"Golga2\"]", "do": null }, { "gene_id": 99439, "description": "dual oxidase 1", "gene_symbol": "[\"Duox1\"]", "do": null }, { "gene_id": 99470, "description": "membrane associated guanylate kinase, WW and PDZ domain containing 3", "gene_symbol": "[\"Magi3\"]", "do": null }, { "gene_id": 99480, "description": "deoxynucleotidyltransferase, terminal, interacting protein 2", "gene_symbol": "[\"Dnttip2\"]", "do": null }, { "gene_id": 99543, "description": "olfactomedin-like 3", "gene_symbol": "[\"Olfml3\"]", "do": null }, { "gene_id": 99571, "description": "fibrinogen gamma chain", "gene_symbol": "[\"Fgg\"]", "do": "[{\"label\":\"congenital afibrinogenemia\",\"id\":\"DOID:2236\"}]" }, { "gene_id": 99586, "description": "dihydropyrimidine dehydrogenase", "gene_symbol": "[\"Dpyd\"]", "do": null }, { "gene_id": 99633, "description": "adhesion G protein-coupled receptor L2", "gene_symbol": "[\"Adgrl2\"]", "do": null }, { "gene_id": 99683, "description": "SEC24 homolog B, COPII coat complex component", "gene_symbol": "[\"Sec24b\"]", "do": null }, { "gene_id": 99709, "description": "chloride channel accessory 4B", "gene_symbol": "[\"Clca4b\"]", "do": null }, { "gene_id": 99712, "description": "choline/ethanolaminephosphotransferase 1", "gene_symbol": "[\"Cept1\"]", "do": null }, { "gene_id": 99738, "description": "potassium voltage gated channel, Shaw-related subfamily, member 4", "gene_symbol": "[\"Kcnc4\"]", "do": null }, { "gene_id": 99929, "description": "TCDD-inducible poly(ADP-ribose) polymerase", "gene_symbol": "[\"Tiparp\"]", "do": null }, { "gene_id": 100019, "description": "midasin AAA ATPase 1", "gene_symbol": "[\"Mdn1\"]", "do": null }, { "gene_id": 100061, "description": "leucine rich repeat containing 19", "gene_symbol": "[\"Lrrc19\"]", "do": null }, { "gene_id": 100102, "description": "proprotein convertase subtilisin/kexin type 9", "gene_symbol": "[\"Pcsk9\"]", "do": null }, { "gene_id": 100169, "description": "phosphatase and actin regulator 4", "gene_symbol": "[\"Phactr4\"]", "do": null }, { "gene_id": 100182, "description": "AT-hook transcription factor", "gene_symbol": "[\"Akna\"]", "do": null }, { "gene_id": 100198, "description": "hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)", "gene_symbol": "[\"H6pd\"]", "do": null }, { "gene_id": 100206, "description": "ADP-ribosylserine hydrolase", "gene_symbol": "[\"Adprs\"]", "do": null }, { "gene_id": 100317, "description": "expressed sequence AU040320", "gene_symbol": "[\"AU040320\"]", "do": null }, { "gene_id": 100340, "description": "sphingomyelin phosphodiesterase, acid-like 3B", "gene_symbol": "[\"Smpdl3b\"]", "do": null }, { "gene_id": 100434, "description": "solute carrier family 44, member 1", "gene_symbol": "[\"Slc44a1\"]", "do": null }, { "gene_id": 100535, "description": "2'-5' oligoadenylate synthetase 1D", "gene_symbol": "[\"Oas1d\"]", "do": null }, { "gene_id": 100559, "description": "UDP glucuronosyltransferase 2 family, polypeptide B38", "gene_symbol": "[\"Ugt2b38\"]", "do": null }, { "gene_id": 100561, "description": "solute carrier family 15, member 4", "gene_symbol": "[\"Slc15a4\"]", "do": null }, { "gene_id": 100604, "description": "leucine rich repeat containing 8 family, member C", "gene_symbol": "[\"Lrrc8c\"]", "do": null }, { "gene_id": 100637, "description": "NEDD4 binding protein 2-like 1", "gene_symbol": "[\"N4bp2l1\"]", "do": null }, { "gene_id": 100647, "description": "uroplakin 3B", "gene_symbol": "[\"Upk3b\"]", "do": null }, { "gene_id": 100689, "description": "spondin 2, extracellular matrix protein", "gene_symbol": "[\"Spon2\"]", "do": null }, { "gene_id": 100705, "description": "acetyl-Coenzyme A carboxylase beta", "gene_symbol": "[\"Acacb\"]", "do": null }, { "gene_id": 100710, "description": "PDS5 cohesin associated factor B", "gene_symbol": "[\"Pds5b\"]", "do": null }, { "gene_id": 100727, "description": "UDP glucuronosyltransferase 2 family, polypeptide B34", "gene_symbol": "[\"Ugt2b34\"]", "do": null }, { "gene_id": 100910, "description": "chondroitin polymerizing factor 2", "gene_symbol": "[\"Chpf2\"]", "do": null }, { "gene_id": 100952, "description": "elastin microfibril interfacer 1", "gene_symbol": "[\"Emilin1\"]", "do": null }, { "gene_id": 101113, "description": "sorting nexin family member 21", "gene_symbol": "[\"Snx21\"]", "do": null }, { "gene_id": 101118, "description": "transmembrane protein 168", "gene_symbol": "[\"Tmem168\"]", "do": null }, { "gene_id": 101187, "description": "poly (ADP-ribose) polymerase family, member 11", "gene_symbol": "[\"Parp11\"]", "do": null }, { "gene_id": 101202, "description": "HEPACAM family member 2", "gene_symbol": "[\"Hepacam2\"]", "do": null }, { "gene_id": 101351, "description": "EGF domain specific O-linked N-acetylglucosamine transferase", "gene_symbol": "[\"Eogt\"]", "do": null }, { "gene_id": 101434, "description": "CEA cell adhesion molecule 15", "gene_symbol": "[\"Ceacam15\"]", "do": null }, { "gene_id": 101471, "description": "PHD and ring finger domains 1", "gene_symbol": "[\"Phrf1\"]", "do": null }, { "gene_id": 101488, "description": "solute carrier organic anion transporter family, member 2b1", "gene_symbol": "[\"Slco2b1\"]", "do": null }, { "gene_id": 101497, "description": "pleckstrin homology domain containing, family G (with RhoGef domain) member 2", "gene_symbol": "[\"Plekhg2\"]", "do": null }, { "gene_id": 101706, "description": "nuclear mitotic apparatus protein 1", "gene_symbol": "[\"Numa1\"]", "do": null }, { "gene_id": 101744, "description": "acid phosphatase 7, tartrate resistant", "gene_symbol": "[\"Acp7\"]", "do": null }, { "gene_id": 101772, "description": "anoctamin 1, calcium activated chloride channel", "gene_symbol": "[\"Ano1\"]", "do": null }, { "gene_id": 101809, "description": "sprouty-related EVH1 domain containing 3", "gene_symbol": "[\"Spred3\"]", "do": null }, { "gene_id": 101883, "description": "IGF-like family receptor 1", "gene_symbol": "[\"Igflr1\"]", "do": null }, { "gene_id": 101943, "description": "splicing factor 3b, subunit 3", "gene_symbol": "[\"Sf3b3\"]", "do": null }, { "gene_id": 101994, "description": "chromosome alignment maintaining phosphoprotein 1", "gene_symbol": "[\"Champ1\"]", "do": null }, { "gene_id": 102022, "description": "carboxylesterase 2A", "gene_symbol": "[\"Ces2a\"]", "do": null }, { "gene_id": 102093, "description": "phosphorylase kinase beta", "gene_symbol": "[\"Phkb\"]", "do": "[{\"label\":\"glycogen storage disease IXb\",\"id\":\"DOID:0111041\"}]" }, { "gene_id": 102103, "description": "mitochondrial tumor suppressor 1", "gene_symbol": "[\"Mtus1\"]", "do": null }, { "gene_id": 102247, "description": "glycerol-3-phosphate acyltransferase 4", "gene_symbol": "[\"Gpat4\"]", "do": null }, { "gene_id": 102278, "description": "copine VII", "gene_symbol": "[\"Cpne7\"]", "do": null }, { "gene_id": 102436, "description": "leucyl-tRNA synthetase, mitochondrial", "gene_symbol": "[\"Lars2\"]", "do": null }, { "gene_id": 102448, "description": "xylulokinase homolog (H. influenzae)", "gene_symbol": "[\"Xylb\"]", "do": null }, { "gene_id": 102570, "description": "solute carrier family 22 (organic cation transporter), member 13", "gene_symbol": "[\"Slc22a13\"]", "do": null }, { "gene_id": 102580, "description": "ALG9 alpha-1,2-mannosyltransferase", "gene_symbol": "[\"Alg9\"]", "do": null }, { "gene_id": 102595, "description": "pleckstrin homology domain containing, family O member 2", "gene_symbol": "[\"Plekho2\"]", "do": null }, { "gene_id": 102607, "description": "sorting nexin 19", "gene_symbol": "[\"Snx19\"]", "do": null }, { "gene_id": 102657, "description": "CD276 antigen", "gene_symbol": "[\"Cd276\"]", "do": null }, { "gene_id": 102680, "description": "solute carrier family 6 (neurotransmitter transporter), member 20A", "gene_symbol": "[\"Slc6a20a\"]", "do": null }, { "gene_id": 102693, "description": "pleckstrin homology like domain, family B, member 1", "gene_symbol": "[\"Phldb1\"]", "do": null }, { "gene_id": 102791, "description": "T cell leukemia translocation altered gene", "gene_symbol": "[\"Tcta\"]", "do": null }, { "gene_id": 102857, "description": "solute carrier family 6 (neurotransmitter transporter, creatine), member 8", "gene_symbol": "[\"Slc6a8\"]", "do": "[{\"label\":\"cerebral creatine deficiency syndrome 1\",\"id\":\"DOID:0050800\"}]" }, { "gene_id": 102866, "description": "plastin 3 (T-isoform)", "gene_symbol": "[\"Pls3\"]", "do": "[{\"label\":\"congenital diaphragmatic hernia\",\"id\":\"DOID:3827\"},{\"label\":\"osteoporosis\",\"id\":\"DOID:11476\"}]" }, { "gene_id": 103080, "description": "septin 10", "gene_symbol": "[\"Septin10\"]", "do": null }, { "gene_id": 103098, "description": "solute carrier family 6 (neurotransmitter transporter), member 15", "gene_symbol": "[\"Slc6a15\"]", "do": null }, { "gene_id": 103266, "description": "transmembrane protein 263", "gene_symbol": "[\"Tmem263\"]", "do": null }, { "gene_id": 103425, "description": "nicalin", "gene_symbol": "[\"Ncln\"]", "do": null }, { "gene_id": 103468, "description": "nucleoporin 107", "gene_symbol": "[\"Nup107\"]", "do": null }, { "gene_id": 103534, "description": "mannoside acetylglucosaminyltransferase 4, isoenzyme B", "gene_symbol": "[\"Mgat4b\"]", "do": null }, { "gene_id": 103694, "description": "transmembrane p24 trafficking protein 4", "gene_symbol": "[\"Tmed4\"]", "do": null }, { "gene_id": 103724, "description": "TBC1 domain family, member 10a", "gene_symbol": "[\"Tbc1d10a\"]", "do": null }, { "gene_id": 103765, "description": "transmembrane protein 17", "gene_symbol": "[\"Tmem17\"]", "do": null }, { "gene_id": 103963, "description": "ribophorin I", "gene_symbol": "[\"Rpn1\"]", "do": null }, { "gene_id": 103967, "description": "dynamin 3", "gene_symbol": "[\"Dnm3\"]", "do": null }, { "gene_id": 103968, "description": "perilipin 1", "gene_symbol": "[\"Plin1\"]", "do": null }, { "gene_id": 103978, "description": "glypican 5", "gene_symbol": "[\"Gpc5\"]", "do": null }, { "gene_id": 103988, "description": "glucokinase", "gene_symbol": "[\"Gck\"]", "do": "[{\"label\":\"familial hyperinsulinemic hypoglycemia 3\",\"id\":\"DOID:0070216\"},{\"label\":\"hyperinsulinemic hypoglycemia\",\"id\":\"DOID:13317\"},{\"label\":\"maturity-onset diabetes of the young type 2\",\"id\":\"DOID:0111100\"},{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 104001, "description": "reticulon 1", "gene_symbol": "[\"Rtn1\"]", "do": null }, { "gene_id": 104009, "description": "quiescin Q6 sulfhydryl oxidase 1", "gene_symbol": "[\"Qsox1\"]", "do": "[{\"label\":\"VACTERL association\",\"id\":\"DOID:14679\"}]" }, { "gene_id": 104010, "description": "cadherin 22", "gene_symbol": "[\"Cdh22\"]", "do": null }, { "gene_id": 104069, "description": "synuclein, beta", "gene_symbol": "[\"Sncb\"]", "do": null }, { "gene_id": 104079, "description": "neurexophilin 3", "gene_symbol": "[\"Nxph3\"]", "do": null }, { "gene_id": 104082, "description": "WD repeat domain 7", "gene_symbol": "[\"Wdr7\"]", "do": null }, { "gene_id": 104099, "description": "integrin alpha 9", "gene_symbol": "[\"Itga9\"]", "do": "[{\"label\":\"congenital chylothorax\",\"id\":\"DOID:0060646\"}]" }, { "gene_id": 104110, "description": "adenylate cyclase 4", "gene_symbol": "[\"Adcy4\"]", "do": null }, { "gene_id": 104111, "description": "adenylate cyclase 3", "gene_symbol": "[\"Adcy3\"]", "do": "[{\"label\":\"major depressive disorder\",\"id\":\"DOID:1470\"}]" }, { "gene_id": 104112, "description": "ATP citrate lyase", "gene_symbol": "[\"Acly\"]", "do": null }, { "gene_id": 104158, "description": "carboxylesterase 1D", "gene_symbol": "[\"Ces1d\"]", "do": null }, { "gene_id": 104174, "description": "glycine decarboxylase", "gene_symbol": "[\"Gldc\"]", "do": "[{\"label\":\"glycine encephalopathy\",\"id\":\"DOID:9268\"}]" }, { "gene_id": 104183, "description": "chitinase-like 4", "gene_symbol": "[\"Chil4\"]", "do": null }, { "gene_id": 104263, "description": "lysine (K)-specific demethylase 3A", "gene_symbol": "[\"Kdm3a\"]", "do": "[{\"label\":\"obesity\",\"id\":\"DOID:9970\"}]" }, { "gene_id": 104318, "description": "casein kinase 1, delta", "gene_symbol": "[\"Csnk1d\"]", "do": "[{\"label\":\"attention deficit hyperactivity disorder\",\"id\":\"DOID:1094\"}]" }, { "gene_id": 104401, "description": "pecanex homolog 3", "gene_symbol": "[\"Pcnx3\"]", "do": null }, { "gene_id": 104416, "description": "Brca1 associated protein 1", "gene_symbol": "[\"Bap1\"]", "do": "[{\"label\":\"myelodysplastic syndrome\",\"id\":\"DOID:0050908\"}]" }, { "gene_id": 104443, "description": "neuropeptide FF receptor 2", "gene_symbol": "[\"Npffr2\"]", "do": null }, { "gene_id": 104458, "description": "arginyl-tRNA synthetase 1", "gene_symbol": "[\"Rars1\"]", "do": null }, { "gene_id": 104570, "description": "protein phosphatase 4 regulatory subunit 3B", "gene_symbol": "[\"Ppp4r3b\"]", "do": null }, { "gene_id": 104721, "description": "DEAD box helicase 1", "gene_symbol": "[\"Ddx1\"]", "do": null }, { "gene_id": 104759, "description": "phospholipase D family member 4", "gene_symbol": "[\"Pld4\"]", "do": "[{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 104771, "description": "JNK1/MAPK8-associated membrane protein", "gene_symbol": "[\"Jkamp\"]", "do": null }, { "gene_id": 104776, "description": "aldehyde dehydrogenase family 6, subfamily A1", "gene_symbol": "[\"Aldh6a1\"]", "do": null }, { "gene_id": 104831, "description": "protein tyrosine phosphatase, non-receptor type 23", "gene_symbol": "[\"Ptpn23\"]", "do": null }, { "gene_id": 104836, "description": "Cbl proto-oncogene like 1", "gene_symbol": "[\"Cbll1\"]", "do": null }, { "gene_id": 104885, "description": "transmembrane protein 179", "gene_symbol": "[\"Tmem179\"]", "do": null }, { "gene_id": 105148, "description": "isoleucyl-tRNA synthetase 1", "gene_symbol": "[\"Iars1\"]", "do": null }, { "gene_id": 105193, "description": "NHL repeat containing 1", "gene_symbol": "[\"Nhlrc1\"]", "do": "[{\"label\":\"Lafora disease\",\"id\":\"DOID:3534\"}]" }, { "gene_id": 105203, "description": "transcription activation suppressor family member 2", "gene_symbol": "[\"Tasor2\"]", "do": null }, { "gene_id": 105298, "description": "ependymin related 1", "gene_symbol": "[\"Epdr1\"]", "do": null }, { "gene_id": 105348, "description": "golgi membrane protein 1", "gene_symbol": "[\"Golm1\"]", "do": null }, { "gene_id": 105355, "description": "solute carrier family 17 (sodium phosphate), member 3", "gene_symbol": "[\"Slc17a3\"]", "do": null }, { "gene_id": 105439, "description": "SLAIN motif family, member 1", "gene_symbol": "[\"Slain1\"]", "do": null }, { "gene_id": 105450, "description": "multimerin 2", "gene_symbol": "[\"Mmrn2\"]", "do": null }, { "gene_id": 105522, "description": "ankyrin repeat domain 28", "gene_symbol": "[\"Ankrd28\"]", "do": null }, { "gene_id": 105653, "description": "phytanoyl-CoA hydroxylase interacting protein", "gene_symbol": "[\"Phyhip\"]", "do": null }, { "gene_id": 105675, "description": "peptidylprolyl isomerase F (cyclophilin F)", "gene_symbol": "[\"Ppif\"]", "do": null }, { "gene_id": 105689, "description": "MYC binding protein 2, E3 ubiquitin protein ligase", "gene_symbol": "[\"Mycbp2\"]", "do": null }, { "gene_id": 105722, "description": "anoctamin 6", "gene_symbol": "[\"Ano6\"]", "do": null }, { "gene_id": 105727, "description": "solute carrier family 38, member 1", "gene_symbol": "[\"Slc38a1\"]", "do": null }, { "gene_id": 105732, "description": "scaffolding CK1 anchoring protein H", "gene_symbol": "[\"Sack1h\"]", "do": null }, { "gene_id": 105787, "description": "protein kinase, AMP-activated, alpha 1 catalytic subunit", "gene_symbol": "[\"Prkaa1\"]", "do": null }, { "gene_id": 105827, "description": "adhesion molecule with Ig like domain 2", "gene_symbol": "[\"Amigo2\"]", "do": null }, { "gene_id": 105847, "description": "lipase maturation factor 2", "gene_symbol": "[\"Lmf2\"]", "do": null }, { "gene_id": 105853, "description": "mal, T cell differentiation protein 2", "gene_symbol": "[\"Mal2\"]", "do": null }, { "gene_id": 105887, "description": "UDP glycosyltransferases 3 family, polypeptide A2", "gene_symbol": "[\"Ugt3a2\"]", "do": null }, { "gene_id": 106014, "description": "TAFA chemokine like family member 5", "gene_symbol": "[\"Tafa5\"]", "do": null }, { "gene_id": 106021, "description": "topoisomerase I binding, arginine/serine-rich", "gene_symbol": "[\"Topors\"]", "do": null }, { "gene_id": 106052, "description": "F-box protein 4", "gene_symbol": "[\"Fbxo4\"]", "do": null }, { "gene_id": 106200, "description": "thioredoxin domain containing 11", "gene_symbol": "[\"Txndc11\"]", "do": null }, { "gene_id": 106248, "description": "queuine tRNA-ribosyltransferase accessory subunit 2", "gene_symbol": "[\"Qtrt2\"]", "do": null }, { "gene_id": 106344, "description": "replication factor C (activator 1) 4", "gene_symbol": "[\"Rfc4\"]", "do": null }, { "gene_id": 106347, "description": "immunoglobulin-like domain containing receptor 1", "gene_symbol": "[\"Ildr1\"]", "do": "[{\"label\":\"autosomal recessive nonsyndromic deafness 42\",\"id\":\"DOID:0110500\"}]" }, { "gene_id": 106393, "description": "sarcalumenin", "gene_symbol": "[\"Srl\"]", "do": null }, { "gene_id": 106407, "description": "solute carrier family 51, alpha subunit", "gene_symbol": "[\"Slc51a\"]", "do": null }, { "gene_id": 106522, "description": "protein kinase domain containing, cytoplasmic", "gene_symbol": "[\"Pkdcc\"]", "do": null }, { "gene_id": 106529, "description": "trans-2,3-enoyl-CoA reductase", "gene_symbol": "[\"Tecr\"]", "do": null }, { "gene_id": 106565, "description": "delta like non-canonical Notch ligand 2", "gene_symbol": "[\"Dlk2\"]", "do": null }, { "gene_id": 106581, "description": "family with sequence similarity 234, member A", "gene_symbol": "[\"Fam234a\"]", "do": null }, { "gene_id": 106583, "description": "SR-related CTD-associated factor 8", "gene_symbol": "[\"Scaf8\"]", "do": null }, { "gene_id": 106672, "description": "small integral membrane protein 29", "gene_symbol": "[\"Smim29\"]", "do": null }, { "gene_id": 106722, "description": "megakaryocyte and platelet inhibitory receptor G6b", "gene_symbol": "[\"Mpig6b\"]", "do": null }, { "gene_id": 106757, "description": "cation channel sperm associated auxiliary subunit delta", "gene_symbol": "[\"Catsperd\"]", "do": null }, { "gene_id": 106759, "description": "TIR domain containing adaptor molecule 1", "gene_symbol": "[\"Ticam1\"]", "do": null }, { "gene_id": 106763, "description": "tau tubulin kinase 1", "gene_symbol": "[\"Ttbk1\"]", "do": null }, { "gene_id": 106821, "description": "O-acyl-ADP-ribose deacylase 1", "gene_symbol": "[\"Oard1\"]", "do": null }, { "gene_id": 106957, "description": "solute carrier family 39 (metal ion transporter), member 6", "gene_symbol": "[\"Slc39a6\"]", "do": null }, { "gene_id": 107035, "description": "F-box protein 38", "gene_symbol": "[\"Fbxo38\"]", "do": null }, { "gene_id": 107065, "description": "leucine rich repeat transmembrane neuronal 2", "gene_symbol": "[\"Lrrtm2\"]", "do": null }, { "gene_id": 107146, "description": "glycine-N-acyltransferase", "gene_symbol": "[\"Glyat\"]", "do": null }, { "gene_id": 107173, "description": "G protein-coupled receptor 137", "gene_symbol": "[\"Gpr137\"]", "do": null }, { "gene_id": 107221, "description": "free fatty acid receptor 4", "gene_symbol": "[\"Ffar4\"]", "do": null }, { "gene_id": 107227, "description": "mono-ADP ribosylhydrolase 1", "gene_symbol": "[\"Macrod1\"]", "do": null }, { "gene_id": 107242, "description": "expressed sequence AI837181", "gene_symbol": "[\"AI837181\"]", "do": null }, { "gene_id": 107250, "description": "Kazal-type serine peptidase inhibitor domain 1", "gene_symbol": "[\"Kazald1\"]", "do": null }, { "gene_id": 107271, "description": "tyrosyl-tRNA synthetase 1", "gene_symbol": "[\"Yars1\"]", "do": "[{\"label\":\"Charcot-Marie-Tooth disease dominant intermediate C\",\"id\":\"DOID:0110199\"}]" }, { "gene_id": 107338, "description": "golgi-specific brefeldin A-resistance factor 1", "gene_symbol": "[\"Gbf1\"]", "do": null }, { "gene_id": 107358, "description": "transmembrane 9 superfamily member 3", "gene_symbol": "[\"Tm9sf3\"]", "do": null }, { "gene_id": 107448, "description": "unc-5 netrin receptor A", "gene_symbol": "[\"Unc5a\"]", "do": null }, { "gene_id": 107449, "description": "unc-5 netrin receptor B", "gene_symbol": "[\"Unc5b\"]", "do": null }, { "gene_id": 107476, "description": "acetyl-Coenzyme A carboxylase alpha", "gene_symbol": "[\"Acaca\"]", "do": null }, { "gene_id": 107508, "description": "glutamyl-prolyl-tRNA synthetase 1", "gene_symbol": "[\"Eprs1\"]", "do": null }, { "gene_id": 107513, "description": "signal sequence receptor, alpha", "gene_symbol": "[\"Ssr1\"]", "do": null }, { "gene_id": 107515, "description": "leucine-rich repeat-containing G protein-coupled receptor 4", "gene_symbol": "[\"Lgr4\"]", "do": "[{\"label\":\"glaucoma\",\"id\":\"DOID:1686\"}]" }, { "gene_id": 107522, "description": "endothelin converting enzyme 2", "gene_symbol": "[\"Ece2\"]", "do": null }, { "gene_id": 107527, "description": "interleukin 1 receptor-like 2", "gene_symbol": "[\"Il1rl2\"]", "do": null }, { "gene_id": 107528, "description": "MAGE family member E1", "gene_symbol": "[\"Magee1\"]", "do": null }, { "gene_id": 107581, "description": "collagen, type XVI, alpha 1", "gene_symbol": "[\"Col16a1\"]", "do": null }, { "gene_id": 107723, "description": "solute carrier family 12, member 6", "gene_symbol": "[\"Slc12a6\"]", "do": "[{\"label\":\"agenesis of the corpus callosum with peripheral neuropathy\",\"id\":\"DOID:0090003\"},{\"label\":\"motor peripheral neuropathy\",\"id\":\"DOID:2477\"}]" }, { "gene_id": 107747, "description": "aldehyde dehydrogenase 1 family, member L1", "gene_symbol": "[\"Aldh1l1\"]", "do": null }, { "gene_id": 107767, "description": "secretory carrier membrane protein 1", "gene_symbol": "[\"Scamp1\"]", "do": null }, { "gene_id": 107831, "description": "adhesion G protein-coupled receptor B1", "gene_symbol": "[\"Adgrb1\"]", "do": null }, { "gene_id": 107849, "description": "prolactin family 2, subfamily c, member 5", "gene_symbol": "[\"Prl2c5\"]", "do": null }, { "gene_id": 107869, "description": "cystathionine gamma lyase", "gene_symbol": "[\"Cth\"]", "do": "[{\"label\":\"cystathioninuria\",\"id\":\"DOID:0090142\"}]" }, { "gene_id": 107895, "description": "mannoside acetylglucosaminyltransferase 5", "gene_symbol": "[\"Mgat5\"]", "do": null }, { "gene_id": 107932, "description": "chromodomain helicase DNA binding protein 4", "gene_symbol": "[\"Chd4\"]", "do": "[{\"label\":\"left ventricular noncompaction\",\"id\":\"DOID:0060480\"}]" }, { "gene_id": 107934, "description": "cadherin, EGF LAG seven-pass G-type receptor 3", "gene_symbol": "[\"Celsr3\"]", "do": null }, { "gene_id": 107939, "description": "nuclear pore membrane protein 121", "gene_symbol": "[\"Pom121\"]", "do": null }, { "gene_id": 107971, "description": "fibroblast growth factor receptor substrate 3", "gene_symbol": "[\"Frs3\"]", "do": null }, { "gene_id": 107975, "description": "phosphofurin acidic cluster sorting protein 1", "gene_symbol": "[\"Pacs1\"]", "do": null }, { "gene_id": 108015, "description": "cholinergic receptor, nicotinic, beta polypeptide 4", "gene_symbol": "[\"Chrnb4\"]", "do": null }, { "gene_id": 108030, "description": "lin-7 homolog A, crumbs cell polarity complex component", "gene_symbol": "[\"Lin7a\"]", "do": null }, { "gene_id": 108037, "description": "serine hydroxymethyltransferase 2 (mitochondrial)", "gene_symbol": "[\"Shmt2\"]", "do": null }, { "gene_id": 108043, "description": "cholinergic receptor, nicotinic, beta polypeptide 3", "gene_symbol": "[\"Chrnb3\"]", "do": null }, { "gene_id": 108052, "description": "solute carrier family 14 (urea transporter), member 1", "gene_symbol": "[\"Slc14a1\"]", "do": null }, { "gene_id": 108058, "description": "calcium/calmodulin-dependent protein kinase II, delta", "gene_symbol": "[\"Camk2d\"]", "do": null }, { "gene_id": 108068, "description": "glutamate receptor, metabotropic 2", "gene_symbol": "[\"Grm2\"]", "do": null }, { "gene_id": 108069, "description": "glutamate receptor, metabotropic 3", "gene_symbol": "[\"Grm3\"]", "do": null }, { "gene_id": 108071, "description": "glutamate receptor, metabotropic 5", "gene_symbol": "[\"Grm5\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 108072, "description": "glutamate receptor, metabotropic 6", "gene_symbol": "[\"Grm6\"]", "do": "[{\"label\":\"congenital stationary night blindness 1B\",\"id\":\"DOID:0110865\"}]" }, { "gene_id": 108073, "description": "glutamate receptor, metabotropic 7", "gene_symbol": "[\"Grm7\"]", "do": null }, { "gene_id": 108075, "description": "latent transforming growth factor beta binding protein 4", "gene_symbol": "[\"Ltbp4\"]", "do": "[{\"label\":\"cutis laxa\",\"id\":\"DOID:3144\"}]" }, { "gene_id": 108078, "description": "oxidized low density lipoprotein (lectin-like) receptor 1", "gene_symbol": "[\"Olr1\"]", "do": null }, { "gene_id": 108079, "description": "protein kinase, AMP-activated, alpha 2 catalytic subunit", "gene_symbol": "[\"Prkaa2\"]", "do": null }, { "gene_id": 108083, "description": "phosphatidylinositol-5-phosphate 4-kinase, type II, beta", "gene_symbol": "[\"Pip4k2b\"]", "do": null }, { "gene_id": 108096, "description": "solute carrier organic anion transporter family, member 1a5", "gene_symbol": "[\"Slco1a5\"]", "do": null }, { "gene_id": 108097, "description": "protein kinase, AMP-activated, beta 2 non-catalytic subunit", "gene_symbol": "[\"Prkab2\"]", "do": null }, { "gene_id": 108099, "description": "protein kinase, AMP-activated, gamma 2 non-catalytic subunit", "gene_symbol": "[\"Prkag2\"]", "do": null }, { "gene_id": 108100, "description": "brain-specific angiogenesis inhibitor 1-associated protein 2", "gene_symbol": "[\"Baiap2\"]", "do": null }, { "gene_id": 108105, "description": "UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5", "gene_symbol": "[\"B3gnt5\"]", "do": null }, { "gene_id": 108115, "description": "solute carrier organic anion transporter family, member 4a1", "gene_symbol": "[\"Slco4a1\"]", "do": null }, { "gene_id": 108116, "description": "solute carrier organic anion transporter family, member 3a1", "gene_symbol": "[\"Slco3a1\"]", "do": null }, { "gene_id": 108121, "description": "U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1", "gene_symbol": "[\"U2af1\"]", "do": null }, { "gene_id": 108143, "description": "TATA-box binding protein associated factor 9", "gene_symbol": "[\"Taf9\"]", "do": null }, { "gene_id": 108148, "description": "polypeptide N-acetylgalactosaminyltransferase 2", "gene_symbol": "[\"Galnt2\"]", "do": null }, { "gene_id": 108150, "description": "polypeptide N-acetylgalactosaminyltransferase 7", "gene_symbol": "[\"Galnt7\"]", "do": null }, { "gene_id": 108151, "description": "sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D", "gene_symbol": "[\"Sema3d\"]", "do": null }, { "gene_id": 108153, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 7", "gene_symbol": "[\"Adamts7\"]", "do": null }, { "gene_id": 108155, "description": "O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase)", "gene_symbol": "[\"Ogt\"]", "do": "[{\"label\":\"congenital disorder of glycosylation\",\"id\":\"DOID:5212\"}]" }, { "gene_id": 108156, "description": "methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase", "gene_symbol": "[\"Mthfd1\"]", "do": null }, { "gene_id": 108652, "description": "solute carrier family 35, member B3", "gene_symbol": "[\"Slc35b3\"]", "do": null }, { "gene_id": 108655, "description": "forkhead box P1", "gene_symbol": "[\"Foxp1\"]", "do": null }, { "gene_id": 108679, "description": "COP9 signalosome subunit 8", "gene_symbol": "[\"Cops8\"]", "do": null }, { "gene_id": 108682, "description": "glutamic pyruvate transaminase (alanine aminotransferase) 2", "gene_symbol": "[\"Gpt2\"]", "do": null }, { "gene_id": 108687, "description": "ER degradation enhancer, mannosidase alpha-like 2", "gene_symbol": "[\"Edem2\"]", "do": null }, { "gene_id": 108705, "description": "pituitary tumor-transforming 1 interacting protein", "gene_symbol": "[\"Pttg1ip\"]", "do": null }, { "gene_id": 108760, "description": "polypeptide N-acetylgalactosaminyltransferase 16", "gene_symbol": "[\"Galnt16\"]", "do": null }, { "gene_id": 108800, "description": "stonin 2", "gene_symbol": "[\"Ston2\"]", "do": null }, { "gene_id": 108829, "description": "jumonji domain containing 1C", "gene_symbol": "[\"Jmjd1c\"]", "do": null }, { "gene_id": 108857, "description": "ankyrin repeat and KH domain containing 1", "gene_symbol": "[\"Ankhd1\"]", "do": null }, { "gene_id": 108902, "description": "beta-1,4-glucuronyltransferase 1", "gene_symbol": "[\"B4gat1\"]", "do": "[{\"label\":\"muscular dystrophy-dystroglycanopathy type B1\",\"id\":\"DOID:0050588\"}]" }, { "gene_id": 108911, "description": "regulator of chromosome condensation 2", "gene_symbol": "[\"Rcc2\"]", "do": null }, { "gene_id": 108946, "description": "zinc finger, ZZ domain containing 3", "gene_symbol": "[\"Zzz3\"]", "do": null }, { "gene_id": 108989, "description": "translocated promoter region, nuclear basket protein", "gene_symbol": "[\"Tpr\"]", "do": null }, { "gene_id": 109032, "description": "Sp110 nuclear body protein", "gene_symbol": "[\"Sp110\"]", "do": null }, { "gene_id": 109065, "description": "dynein, axonemal assembly factor 2", "gene_symbol": "[\"Dnaaf2\"]", "do": "[{\"label\":\"primary ciliary dyskinesia 10\",\"id\":\"DOID:0110612\"}]" }, { "gene_id": 109135, "description": "pleckstrin homology domain containing, family A member 5", "gene_symbol": "[\"Plekha5\"]", "do": null }, { "gene_id": 109151, "description": "chromodomain helicase DNA binding protein 9", "gene_symbol": "[\"Chd9\"]", "do": null }, { "gene_id": 109154, "description": "malectin", "gene_symbol": "[\"Mlec\"]", "do": null }, { "gene_id": 109168, "description": "atlastin GTPase 3", "gene_symbol": "[\"Atl3\"]", "do": null }, { "gene_id": 109222, "description": "retinoic acid receptor responder (tazarotene induced) 1", "gene_symbol": "[\"Rarres1\"]", "do": "[{\"label\":\"follicular lymphoma\",\"id\":\"DOID:0050873\"}]" }, { "gene_id": 109232, "description": "saccharopine dehydrogenase (putative)", "gene_symbol": "[\"Sccpdh\"]", "do": null }, { "gene_id": 109242, "description": "kinesin family member 24", "gene_symbol": "[\"Kif24\"]", "do": null }, { "gene_id": 109246, "description": "tetraspanin 9", "gene_symbol": "[\"Tspan9\"]", "do": null }, { "gene_id": 109305, "description": "ORAI calcium release-activated calcium modulator 1", "gene_symbol": "[\"Orai1\"]", "do": null }, { "gene_id": 109331, "description": "ring finger protein 20", "gene_symbol": "[\"Rnf20\"]", "do": null }, { "gene_id": 109332, "description": "CUB domain containing protein 1", "gene_symbol": "[\"Cdcp1\"]", "do": null }, { "gene_id": 109342, "description": "solute carrier family 5 (sodium/glucose cotransporter), member 10", "gene_symbol": "[\"Slc5a10\"]", "do": null }, { "gene_id": 109349, "description": "family with sequence similarity 163, member B", "gene_symbol": "[\"Fam163b\"]", "do": null }, { "gene_id": 109637, "description": "uroplakin 1A", "gene_symbol": "[\"Upk1a\"]", "do": null }, { "gene_id": 109652, "description": "aminoacylase 1", "gene_symbol": "[\"Acy1\"]", "do": null }, { "gene_id": 109658, "description": "taxilin alpha", "gene_symbol": "[\"Txlna\"]", "do": null }, { "gene_id": 109660, "description": "chymotrypsin-like", "gene_symbol": "[\"Ctrl\"]", "do": null }, { "gene_id": 109676, "description": "ankyrin 2, brain", "gene_symbol": "[\"Ank2\"]", "do": "[{\"label\":\"ankyrin-B-related cardiac arrhythmia\",\"id\":\"DOID:0111700\"},{\"label\":\"autistic disorder\",\"id\":\"DOID:12849\"},{\"label\":\"sinoatrial node disease\",\"id\":\"DOID:0050824\"}]" }, { "gene_id": 109685, "description": "hyaluronoglucosaminidase 3", "gene_symbol": "[\"Hyal3\"]", "do": null }, { "gene_id": 109689, "description": "arrestin, beta 1", "gene_symbol": "[\"Arrb1\"]", "do": null }, { "gene_id": 109700, "description": "integrin alpha 1", "gene_symbol": "[\"Itga1\"]", "do": null }, { "gene_id": 109731, "description": "monoamine oxidase B", "gene_symbol": "[\"Maob\"]", "do": null }, { "gene_id": 109778, "description": "biliverdin reductase A", "gene_symbol": "[\"Blvra\"]", "do": null }, { "gene_id": 109785, "description": "phosphoglucomutase 3", "gene_symbol": "[\"Pgm3\"]", "do": null }, { "gene_id": 109821, "description": "coagulation factor XI", "gene_symbol": "[\"F11\"]", "do": "[{\"label\":\"factor XI deficiency\",\"id\":\"DOID:2229\"}]" }, { "gene_id": 109828, "description": "complement component 7", "gene_symbol": "[\"C7\"]", "do": null }, { "gene_id": 109880, "description": "B-Raf proto-oncogene, serine/threonine kinase", "gene_symbol": "[\"Braf\"]", "do": "[{\"label\":\"Langerhans-cell histiocytosis\",\"id\":\"DOID:2571\"},{\"label\":\"cardiofaciocutaneous syndrome\",\"id\":\"DOID:0060233\"},{\"label\":\"melanoma\",\"id\":\"DOID:1909\"},{\"label\":\"papillary thyroid carcinoma\",\"id\":\"DOID:3969\"}]" }, { "gene_id": 109900, "description": "argininosuccinate lyase", "gene_symbol": "[\"Asl\"]", "do": "[{\"label\":\"argininosuccinic aciduria\",\"id\":\"DOID:14755\"}]" }, { "gene_id": 109901, "description": "chymotrypsin-like elastase family, member 1", "gene_symbol": "[\"Cela1\"]", "do": null }, { "gene_id": 109959, "description": "amylase 2a5", "gene_symbol": "[\"Amy2a5\"]", "do": null }, { "gene_id": 109978, "description": "ADP-ribosyltransferase 4", "gene_symbol": "[\"Art4\"]", "do": null }, { "gene_id": 109979, "description": "ADP-ribosyltransferase 3", "gene_symbol": "[\"Art3\"]", "do": null }, { "gene_id": 110006, "description": "glucuronidase, beta", "gene_symbol": "[\"Gusb\"]", "do": "[{\"label\":\"mucopolysaccharidosis type VII\",\"id\":\"DOID:12803\"}]" }, { "gene_id": 110033, "description": "kinesin family member 22", "gene_symbol": "[\"Kif22\"]", "do": null }, { "gene_id": 110075, "description": "bone morphogenetic protein 3", "gene_symbol": "[\"Bmp3\"]", "do": null }, { "gene_id": 110078, "description": "brain glycogen phosphorylase", "gene_symbol": "[\"Pygb\"]", "do": null }, { "gene_id": 110082, "description": "dynein, axonemal, heavy chain 5", "gene_symbol": "[\"Dnah5\"]", "do": "[{\"label\":\"Kartagener syndrome\",\"id\":\"DOID:0050144\"},{\"label\":\"otitis media\",\"id\":\"DOID:10754\"},{\"label\":\"primary ciliary dyskinesia 3\",\"id\":\"DOID:0110599\"},{\"label\":\"primary ciliary dyskinesia\",\"id\":\"DOID:9562\"},{\"label\":\"tetralogy of Fallot\",\"id\":\"DOID:6419\"},{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 110094, "description": "phosphorylase kinase alpha 2", "gene_symbol": "[\"Phka2\"]", "do": null }, { "gene_id": 110095, "description": "liver glycogen phosphorylase", "gene_symbol": "[\"Pygl\"]", "do": "[{\"label\":\"glycogen storage disease VI\",\"id\":\"DOID:2754\"}]" }, { "gene_id": 110119, "description": "mannose phosphate isomerase", "gene_symbol": "[\"Mpi\"]", "do": null }, { "gene_id": 110135, "description": "fibrinogen beta chain", "gene_symbol": "[\"Fgb\"]", "do": null }, { "gene_id": 110168, "description": "G protein-coupled receptor 18", "gene_symbol": "[\"Gpr18\"]", "do": null }, { "gene_id": 110173, "description": "mannosidase, beta A, lysosomal", "gene_symbol": "[\"Manba\"]", "do": "[{\"label\":\"beta-mannosidosis\",\"id\":\"DOID:3633\"}]" }, { "gene_id": 110208, "description": "phosphogluconate dehydrogenase", "gene_symbol": "[\"Pgd\"]", "do": null }, { "gene_id": 110253, "description": "TRIO and F-actin binding protein", "gene_symbol": "[\"Triobp\"]", "do": "[{\"label\":\"autosomal recessive nonsyndromic deafness 28\",\"id\":\"DOID:0110486\"}]" }, { "gene_id": 110265, "description": "methionine sulfoxide reductase A", "gene_symbol": "[\"Msra\"]", "do": null }, { "gene_id": 110279, "description": "BCR activator of RhoGEF and GTPase", "gene_symbol": "[\"Bcr\"]", "do": null }, { "gene_id": 110304, "description": "glycine receptor, alpha 3 subunit", "gene_symbol": "[\"Glra3\"]", "do": null }, { "gene_id": 110308, "description": "keratin 5", "gene_symbol": "[\"Krt5\"]", "do": "[{\"label\":\"generalized severe epidermolysis bullosa simplex 1A\",\"id\":\"DOID:0060735\"}]" }, { "gene_id": 110310, "description": "keratin 7", "gene_symbol": "[\"Krt7\"]", "do": null }, { "gene_id": 110323, "description": "cytochrome c oxidase, subunit 6B1", "gene_symbol": "[\"Cox6b1\"]", "do": null }, { "gene_id": 110326, "description": "taste receptor, type 1, member 1", "gene_symbol": "[\"Tas1r1\"]", "do": null }, { "gene_id": 110350, "description": "dynein cytoplasmic 2 heavy chain 1", "gene_symbol": "[\"Dync2h1\"]", "do": "[{\"label\":\"VACTERL association\",\"id\":\"DOID:14679\"},{\"label\":\"asphyxiating thoracic dystrophy 3\",\"id\":\"DOID:0110087\"}]" }, { "gene_id": 110351, "description": "Rap1 GTPase-activating protein", "gene_symbol": "[\"Rap1gap\"]", "do": null }, { "gene_id": 110382, "description": "complement component 8, beta polypeptide", "gene_symbol": "[\"C8b\"]", "do": null }, { "gene_id": 110460, "description": "acetyl-Coenzyme A acetyltransferase 2", "gene_symbol": "[\"Acat2\"]", "do": null }, { "gene_id": 110542, "description": "anti-Mullerian hormone type 2 receptor", "gene_symbol": "[\"Amhr2\"]", "do": "[{\"label\":\"persistent Mullerian duct syndrome\",\"id\":\"DOID:0050791\"}]" }, { "gene_id": 110557, "description": "histocompatibility 2, Q region locus 6", "gene_symbol": "[\"H2-Q6\"]", "do": null }, { "gene_id": 110558, "description": "histocompatibility 2, Q region locus 9", "gene_symbol": "[\"H2-Q9\"]", "do": null }, { "gene_id": 110596, "description": "Rho guanine nucleotide exchange factor 28", "gene_symbol": "[\"Arhgef28\"]", "do": null }, { "gene_id": 110611, "description": "high density lipoprotein (HDL) binding protein", "gene_symbol": "[\"Hdlbp\"]", "do": null }, { "gene_id": 110637, "description": "glutamate receptor, ionotropic, kainate 4", "gene_symbol": "[\"Grik4\"]", "do": null }, { "gene_id": 110639, "description": "phosphoribosyl pyrophosphate synthetase 2", "gene_symbol": "[\"Prps2\"]", "do": null }, { "gene_id": 110695, "description": "aldehyde dehydrogenase family 7, member A1", "gene_symbol": "[\"Aldh7a1\"]", "do": "[{\"label\":\"pyridoxine-dependent epilepsy\",\"id\":\"DOID:0080768\"}]" }, { "gene_id": 110751, "description": "a disintegrin and metallopeptidase domain 33", "gene_symbol": "[\"Adam33\"]", "do": null }, { "gene_id": 110834, "description": "cholinergic receptor, nicotinic, alpha polypeptide 3", "gene_symbol": "[\"Chrna3\"]", "do": null }, { "gene_id": 110835, "description": "cholinergic receptor, nicotinic, alpha polypeptide 5", "gene_symbol": "[\"Chrna5\"]", "do": null }, { "gene_id": 110854, "description": "protein phosphatase 2 protein activator", "gene_symbol": "[\"Ptpa\"]", "do": null }, { "gene_id": 110862, "description": "potassium voltage-gated channel, subfamily Q, member 3", "gene_symbol": "[\"Kcnq3\"]", "do": "[{\"label\":\"benign neonatal seizures\",\"id\":\"DOID:14264\"}]" }, { "gene_id": 110876, "description": "sodium channel, voltage-gated, type II, alpha", "gene_symbol": "[\"Scn2a\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 110877, "description": "solute carrier family 18 (vesicular monoamine), member 1", "gene_symbol": "[\"Slc18a1\"]", "do": null }, { "gene_id": 110880, "description": "sodium channel, voltage-gated, type IV, alpha", "gene_symbol": "[\"Scn4a\"]", "do": "[{\"label\":\"hyperkalemic periodic paralysis\",\"id\":\"DOID:14451\"},{\"label\":\"hypokalemic periodic paralysis\",\"id\":\"DOID:14452\"}]" }, { "gene_id": 110886, "description": "gamma-aminobutyric acid type A receptor subunit alpha 5", "gene_symbol": "[\"Gabra5\"]", "do": null }, { "gene_id": 110891, "description": "solute carrier family 8 (sodium/calcium exchanger), member 2", "gene_symbol": "[\"Slc8a2\"]", "do": null }, { "gene_id": 110893, "description": "solute carrier family 8 (sodium/calcium exchanger), member 3", "gene_symbol": "[\"Slc8a3\"]", "do": null }, { "gene_id": 110895, "description": "solute carrier family 9 (sodium/hydrogen exchanger), member 4", "gene_symbol": "[\"Slc9a4\"]", "do": null }, { "gene_id": 110902, "description": "cholinergic receptor nicotinic alpha 2 subunit", "gene_symbol": "[\"Chrna2\"]", "do": null }, { "gene_id": 110911, "description": "CDP-diacylglycerol synthase 2", "gene_symbol": "[\"Cds2\"]", "do": null }, { "gene_id": 110920, "description": "heat shock protein family A (Hsp70) member 13", "gene_symbol": "[\"Hspa13\"]", "do": null }, { "gene_id": 110960, "description": "threonyl-tRNA synthetase 1", "gene_symbol": "[\"Tars1\"]", "do": null }, { "gene_id": 111173, "description": "ELKS/RAB6-interacting/CAST family member 1", "gene_symbol": "[\"Erc1\"]", "do": null }, { "gene_id": 111174, "description": "trace amine-associated receptor 1", "gene_symbol": "[\"Taar1\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 112405, "description": "egl-9 family hypoxia-inducible factor 1", "gene_symbol": "[\"Egln1\"]", "do": null }, { "gene_id": 112406, "description": "egl-9 family hypoxia-inducible factor 2", "gene_symbol": "[\"Egln2\"]", "do": null }, { "gene_id": 112408, "description": "taste receptor, type 2, member 116", "gene_symbol": "[\"Tas2r116\"]", "do": null }, { "gene_id": 112417, "description": "UDP glucuronosyltransferase 2 family, polypeptide B37", "gene_symbol": "[\"Ugt2b37\"]", "do": null }, { "gene_id": 113845, "description": "vomeronasal 1 receptor 48", "gene_symbol": "[\"Vmn1r48\"]", "do": null }, { "gene_id": 113846, "description": "vomeronasal 1 receptor 47", "gene_symbol": "[\"Vmn1r47\"]", "do": null }, { "gene_id": 113847, "description": "vomeronasal 1 receptor 43", "gene_symbol": "[\"Vmn1r43\"]", "do": null }, { "gene_id": 113848, "description": "vomeronasal 1 receptor 42", "gene_symbol": "[\"Vmn1r42\"]", "do": null }, { "gene_id": 113849, "description": "vomeronasal 1 receptor 52", "gene_symbol": "[\"Vmn1r52\"]", "do": null }, { "gene_id": 113850, "description": "vomeronasal 1 receptor, A8", "gene_symbol": "[\"V1ra8\"]", "do": null }, { "gene_id": 113852, "description": "vomeronasal 1 receptor 50", "gene_symbol": "[\"Vmn1r50\"]", "do": null }, { "gene_id": 113854, "description": "vomeronasal 1 receptor 44", "gene_symbol": "[\"Vmn1r44\"]", "do": null }, { "gene_id": 113855, "description": "vomeronasal 1 receptor 40", "gene_symbol": "[\"Vmn1r40\"]", "do": null }, { "gene_id": 113856, "description": "vomeronasal 1 receptor 46", "gene_symbol": "[\"Vmn1r46\"]", "do": null }, { "gene_id": 113857, "description": "vomeronasal 1 receptor 41", "gene_symbol": "[\"Vmn1r41\"]", "do": null }, { "gene_id": 113868, "description": "acetyl-Coenzyme A acyltransferase 1A", "gene_symbol": "[\"Acaa1a\"]", "do": null }, { "gene_id": 114229, "description": "KISS1 receptor", "gene_symbol": "[\"Kiss1r\"]", "do": "[{\"label\":\"hypogonadotropic hypogonadism 8 with or without anosmia\",\"id\":\"DOID:0090074\"}]" }, { "gene_id": 114301, "description": "palmdelphin", "gene_symbol": "[\"Palmd\"]", "do": null }, { "gene_id": 114304, "description": "solute carrier family 28 (sodium-coupled nucleoside transporter), member 3", "gene_symbol": "[\"Slc28a3\"]", "do": null }, { "gene_id": 114332, "description": "lymphatic vessel endothelial hyaluronan receptor 1", "gene_symbol": "[\"Lyve1\"]", "do": null }, { "gene_id": 114584, "description": "chloride intracellular channel 1", "gene_symbol": "[\"Clic1\"]", "do": null }, { "gene_id": 114601, "description": "EH domain binding protein 1-like 1", "gene_symbol": "[\"Ehbp1l1\"]", "do": null }, { "gene_id": 114643, "description": "2'-5' oligoadenylate synthetase 1C", "gene_symbol": "[\"Oas1c\"]", "do": null }, { "gene_id": 114644, "description": "solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3", "gene_symbol": "[\"Slc13a3\"]", "do": null }, { "gene_id": 114652, "description": "lymphocyte antigen 6 family member G5C", "gene_symbol": "[\"Ly6g5c\"]", "do": null }, { "gene_id": 114654, "description": "lymphocyte antigen 6 family member G6D", "gene_symbol": "[\"Ly6g6d\"]", "do": null }, { "gene_id": 114661, "description": "serine protease 28", "gene_symbol": "[\"Prss28\"]", "do": null }, { "gene_id": 114662, "description": "serine protease 29", "gene_symbol": "[\"Prss29\"]", "do": null }, { "gene_id": 114715, "description": "sprouty protein with EVH-1 domain 1, related sequence", "gene_symbol": "[\"Spred1\"]", "do": null }, { "gene_id": 114741, "description": "SPT16, facilitates chromatin remodeling subunit", "gene_symbol": "[\"Supt16\"]", "do": null }, { "gene_id": 114863, "description": "pyridoxal phosphate binding protein", "gene_symbol": "[\"Plpbp\"]", "do": null }, { "gene_id": 114873, "description": "DS cell adhesion molecule like 1", "gene_symbol": "[\"Dscaml1\"]", "do": null }, { "gene_id": 114874, "description": "DDHD domain containing 1", "gene_symbol": "[\"Ddhd1\"]", "do": null }, { "gene_id": 114886, "description": "cytoglobin", "gene_symbol": "[\"Cygb\"]", "do": null }, { "gene_id": 116701, "description": "fibroblast growth factor receptor-like 1", "gene_symbol": "[\"Fgfrl1\"]", "do": "[{\"label\":\"Wolf-Hirschhorn syndrome\",\"id\":\"DOID:0050460\"}]" }, { "gene_id": 116837, "description": "regulating synaptic membrane exocytosis 1", "gene_symbol": "[\"Rims1\"]", "do": null }, { "gene_id": 116838, "description": "regulating synaptic membrane exocytosis 2", "gene_symbol": "[\"Rims2\"]", "do": null }, { "gene_id": 116847, "description": "proline arginine-rich end leucine-rich repeat", "gene_symbol": "[\"Prelp\"]", "do": null }, { "gene_id": 116849, "description": "interleukin 22B", "gene_symbol": "[\"Il22b\"]", "do": null }, { "gene_id": 116873, "description": "stromal interaction molecule 2", "gene_symbol": "[\"Stim2\"]", "do": null }, { "gene_id": 116904, "description": "alpha-kinase 3", "gene_symbol": "[\"Alpk3\"]", "do": null }, { "gene_id": 116914, "description": "solute carrier family 19 (thiamine transporter), member 2", "gene_symbol": "[\"Slc19a2\"]", "do": "[{\"label\":\"thiamine-responsive megaloblastic anemia syndrome\",\"id\":\"DOID:0090117\"}]" }, { "gene_id": 116939, "description": "patatin-like phospholipase domain containing 3", "gene_symbol": "[\"Pnpla3\"]", "do": "[{\"label\":\"metabolic dysfunction-associated steatotic liver disease\",\"id\":\"DOID:0080208\"}]" }, { "gene_id": 117160, "description": "tweety family member 2", "gene_symbol": "[\"Ttyh2\"]", "do": null }, { "gene_id": 117167, "description": "STEAP family member 4", "gene_symbol": "[\"Steap4\"]", "do": null }, { "gene_id": 117586, "description": "alpha-1-B glycoprotein", "gene_symbol": "[\"A1bg\"]", "do": null }, { "gene_id": 117589, "description": "ankyrin repeat and SOCS box-containing 7", "gene_symbol": "[\"Asb7\"]", "do": null }, { "gene_id": 117591, "description": "solute carrier family 2 (facilitated glucose transporter), member 9", "gene_symbol": "[\"Slc2a9\"]", "do": "[{\"label\":\"abdominal obesity-metabolic syndrome\",\"id\":\"DOID:0060611\"},{\"label\":\"hyperuricemia\",\"id\":\"DOID:1920\"}]" }, { "gene_id": 117592, "description": "UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6", "gene_symbol": "[\"B3galt6\"]", "do": null }, { "gene_id": 117600, "description": "SLIT-ROBO Rho GTPase activating protein 1", "gene_symbol": "[\"Srgap1\"]", "do": "[{\"label\":\"focal segmental glomerulosclerosis\",\"id\":\"DOID:1312\"}]" }, { "gene_id": 117606, "description": "BOC cell adhesion associated, oncogene regulated", "gene_symbol": "[\"Boc\"]", "do": null }, { "gene_id": 118445, "description": "Kruppel-like transcription factor 16", "gene_symbol": "[\"Klf16\"]", "do": null }, { "gene_id": 118449, "description": "synaptopodin 2", "gene_symbol": "[\"Synpo2\"]", "do": null }, { "gene_id": 121021, "description": "chondroitin sulfate proteoglycan 4", "gene_symbol": "[\"Cspg4\"]", "do": null }, { "gene_id": 140474, "description": "mucin 4", "gene_symbol": "[\"Muc4\"]", "do": "[{\"label\":\"Coronavirus infectious disease\",\"id\":\"DOID:0080599\"}]" }, { "gene_id": 140476, "description": "stereocilin", "gene_symbol": "[\"Strc\"]", "do": "[{\"label\":\"autosomal recessive nonsyndromic deafness 16\",\"id\":\"DOID:0110471\"}]" }, { "gene_id": 140481, "description": "mannosidase 2, alpha 2", "gene_symbol": "[\"Man2a2\"]", "do": null }, { "gene_id": 140483, "description": "histamine N-methyltransferase", "gene_symbol": "[\"Hnmt\"]", "do": null }, { "gene_id": 140484, "description": "protein O-fucosyltransferase 1", "gene_symbol": "[\"Pofut1\"]", "do": null }, { "gene_id": 140488, "description": "insulin-like growth factor 2 mRNA binding protein 3", "gene_symbol": "[\"Igf2bp3\"]", "do": null }, { "gene_id": 140491, "description": "protein phosphatase 1, regulatory subunit 3A", "gene_symbol": "[\"Ppp1r3a\"]", "do": "[{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 140492, "description": "potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2", "gene_symbol": "[\"Kcnn2\"]", "do": "[{\"label\":\"Parkinson's disease\",\"id\":\"DOID:14330\"}]" }, { "gene_id": 140493, "description": "potassium intermediate/small conductance calcium-activated channel, subfamily N, member 3", "gene_symbol": "[\"Kcnn3\"]", "do": null }, { "gene_id": 140497, "description": "CD300C molecule 2", "gene_symbol": "[\"Cd300c2\"]", "do": null }, { "gene_id": 140498, "description": "relaxin/insulin-like family peptide receptor 2", "gene_symbol": "[\"Rxfp2\"]", "do": null }, { "gene_id": 140559, "description": "immunoglobulin superfamily, member 8", "gene_symbol": "[\"Igsf8\"]", "do": null }, { "gene_id": 140570, "description": "plexin B2", "gene_symbol": "[\"Plxnb2\"]", "do": null }, { "gene_id": 140571, "description": "plexin B3", "gene_symbol": "[\"Plxnb3\"]", "do": null }, { "gene_id": 140580, "description": "engulfment and cell motility 1", "gene_symbol": "[\"Elmo1\"]", "do": null }, { "gene_id": 140630, "description": "ubiquitination factor E4A", "gene_symbol": "[\"Ube4a\"]", "do": null }, { "gene_id": 140703, "description": "EMI domain containing 1", "gene_symbol": "[\"Emid1\"]", "do": null }, { "gene_id": 140709, "description": "collagen, type XXVI, alpha 1", "gene_symbol": "[\"Col26a1\"]", "do": null }, { "gene_id": 140721, "description": "CASK-interacting protein 2", "gene_symbol": "[\"Caskin2\"]", "do": null }, { "gene_id": 140740, "description": "SEC63 homolog, protein translocation regulator", "gene_symbol": "[\"Sec63\"]", "do": null }, { "gene_id": 140741, "description": "G protein-coupled receptor 6", "gene_symbol": "[\"Gpr6\"]", "do": null }, { "gene_id": 140765, "description": "transmembrane protease, serine 3", "gene_symbol": "[\"Tmprss3\"]", "do": null }, { "gene_id": 140780, "description": "BMP2 inducible kinase", "gene_symbol": "[\"Bmp2k\"]", "do": null }, { "gene_id": 140781, "description": "myosin, heavy polypeptide 7, cardiac muscle, beta", "gene_symbol": "[\"Myh7\"]", "do": null }, { "gene_id": 140792, "description": "collectin sub-family member 12", "gene_symbol": "[\"Colec12\"]", "do": null }, { "gene_id": 140795, "description": "purinergic receptor P2Y, G-protein coupled, 14", "gene_symbol": "[\"P2ry14\"]", "do": null }, { "gene_id": 140806, "description": "interleukin 25", "gene_symbol": "[\"Il25\"]", "do": null }, { "gene_id": 140919, "description": "solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6", "gene_symbol": "[\"Slc17a6\"]", "do": null }, { "gene_id": 142681, "description": "solute carrier family 34 (sodium phosphate), member 3", "gene_symbol": "[\"Slc34a3\"]", "do": null }, { "gene_id": 142682, "description": "zinc finger, CCHC domain containing 14", "gene_symbol": "[\"Zcchc14\"]", "do": null }, { "gene_id": 142980, "description": "toll-like receptor 3", "gene_symbol": "[\"Tlr3\"]", "do": null }, { "gene_id": 170439, "description": "ELOVL fatty acid elongase 6", "gene_symbol": "[\"Elovl6\"]", "do": null }, { "gene_id": 170458, "description": "glycoprotein hormone alpha 2", "gene_symbol": "[\"Gpha2\"]", "do": null }, { "gene_id": 170483, "description": "glutamate receptor, ionotropic, NMDA3B", "gene_symbol": "[\"Grin3b\"]", "do": null }, { "gene_id": 170571, "description": "contactin associated protein-like 4", "gene_symbol": "[\"Cntnap4\"]", "do": null }, { "gene_id": 170574, "description": "Sp7 transcription factor 7", "gene_symbol": "[\"Sp7\"]", "do": null }, { "gene_id": 170638, "description": "hippocalcin-like 4", "gene_symbol": "[\"Hpcal4\"]", "do": null }, { "gene_id": 170639, "description": "olfactory receptor family 51 subfamily E member 2", "gene_symbol": "[\"Or51e2\"]", "do": null }, { "gene_id": 170643, "description": "kirre like nephrin family adhesion molecule 1", "gene_symbol": "[\"Kirrel1\"]", "do": null }, { "gene_id": 170644, "description": "ubinuclein 1", "gene_symbol": "[\"Ubn1\"]", "do": null }, { "gene_id": 170677, "description": "cadherin-related family member 1", "gene_symbol": "[\"Cdhr1\"]", "do": null }, { "gene_id": 170711, "description": "OTU domain containing 7A", "gene_symbol": "[\"Otud7a\"]", "do": null }, { "gene_id": 170719, "description": "oxidation resistance 1", "gene_symbol": "[\"Oxr1\"]", "do": null }, { "gene_id": 170728, "description": "reticulon 4 interacting protein 1", "gene_symbol": "[\"Rtn4ip1\"]", "do": null }, { "gene_id": 170733, "description": "killer cell lectin-like receptor, subfamily A, member 17", "gene_symbol": "[\"Klra17\"]", "do": null }, { "gene_id": 170738, "description": "potassium voltage-gated channel, subfamily H (eag-related), member 7", "gene_symbol": "[\"Kcnh7\"]", "do": null }, { "gene_id": 170741, "description": "paired immunoglobin-like type 2 receptor beta 1", "gene_symbol": "[\"Pilrb1\"]", "do": null }, { "gene_id": 170743, "description": "toll-like receptor 7", "gene_symbol": "[\"Tlr7\"]", "do": "[{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 170744, "description": "toll-like receptor 8", "gene_symbol": "[\"Tlr8\"]", "do": null }, { "gene_id": 170745, "description": "X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound", "gene_symbol": "[\"Xpnpep2\"]", "do": null }, { "gene_id": 170752, "description": "beta-carotene oxygenase 2", "gene_symbol": "[\"Bco2\"]", "do": null }, { "gene_id": 170753, "description": "zinc finger protein 704", "gene_symbol": "[\"Zfp704\"]", "do": null }, { "gene_id": 170756, "description": "solute carrier family 8 (sodium/lithium/calcium exchanger), member B1", "gene_symbol": "[\"Slc8b1\"]", "do": null }, { "gene_id": 170757, "description": "adhesion G protein-coupled receptor L4", "gene_symbol": "[\"Adgrl4\"]", "do": null }, { "gene_id": 170759, "description": "ATPase type 13A1", "gene_symbol": "[\"Atp13a1\"]", "do": null }, { "gene_id": 170762, "description": "nucleoporin 155", "gene_symbol": "[\"Nup155\"]", "do": null }, { "gene_id": 170771, "description": "KH domain containing, RNA binding, signal transduction associated 2", "gene_symbol": "[\"Khdrbs2\"]", "do": null }, { "gene_id": 170776, "description": "CD209c antigen", "gene_symbol": "[\"Cd209c\"]", "do": null }, { "gene_id": 170779, "description": "CD209d antigen", "gene_symbol": "[\"Cd209d\"]", "do": null }, { "gene_id": 170786, "description": "CD209a antigen", "gene_symbol": "[\"Cd209a\"]", "do": null }, { "gene_id": 170788, "description": "crumbs family member 1, photoreceptor morphogenesis associated", "gene_symbol": "[\"Crb1\"]", "do": "[{\"label\":\"Leber congenital amaurosis 8\",\"id\":\"DOID:0110079\"},{\"label\":\"retinitis pigmentosa 12\",\"id\":\"DOID:0110358\"}]" }, { "gene_id": 170789, "description": "acyl-CoA thioesterase 8", "gene_symbol": "[\"Acot8\"]", "do": null }, { "gene_id": 170829, "description": "translocating chain-associating membrane protein 2", "gene_symbol": "[\"Tram2\"]", "do": null }, { "gene_id": 170835, "description": "inositol polyphosphate 5-phosphatase J", "gene_symbol": "[\"Inpp5j\"]", "do": null }, { "gene_id": 170935, "description": "glutamate receptor, ionotropic, delta 2 (Grid2) interacting protein 1", "gene_symbol": "[\"Grid2ip\"]", "do": null }, { "gene_id": 170952, "description": "proline rich membrane anchor 1", "gene_symbol": "[\"Prima1\"]", "do": null }, { "gene_id": 171095, "description": "interleukin 17 receptor C", "gene_symbol": "[\"Il17rc\"]", "do": null }, { "gene_id": 171166, "description": "mucolipin 3", "gene_symbol": "[\"Mcoln3\"]", "do": null }, { "gene_id": 171167, "description": "protein O-fucosyltransferase 3", "gene_symbol": "[\"Pofut3\"]", "do": null }, { "gene_id": 171171, "description": "netrin G2", "gene_symbol": "[\"Ntng2\"]", "do": null }, { "gene_id": 171209, "description": "acid-sensing ion channel 3", "gene_symbol": "[\"Asic3\"]", "do": null }, { "gene_id": 171212, "description": "polypeptide N-acetylgalactosaminyltransferase 10", "gene_symbol": "[\"Galnt10\"]", "do": null }, { "gene_id": 171257, "description": "vomeronasal 1 receptor 195", "gene_symbol": "[\"Vmn1r195\"]", "do": null }, { "gene_id": 171283, "description": "hepatitis A virus cellular receptor 1", "gene_symbol": "[\"Havcr1\"]", "do": null }, { "gene_id": 171284, "description": "T cell immunoglobulin and mucin domain containing 2", "gene_symbol": "[\"Timd2\"]", "do": null }, { "gene_id": 171285, "description": "hepatitis A virus cellular receptor 2", "gene_symbol": "[\"Havcr2\"]", "do": null }, { "gene_id": 171382, "description": "transient receptor potential cation channel, subfamily M, member 8", "gene_symbol": "[\"Trpm8\"]", "do": null }, { "gene_id": 171405, "description": "solute carrier family 22, member 27", "gene_symbol": "[\"Slc22a27\"]", "do": null }, { "gene_id": 171429, "description": "solute carrier family 26, member 6", "gene_symbol": "[\"Slc26a6\"]", "do": null }, { "gene_id": 171463, "description": "interleukin 17 receptor D", "gene_symbol": "[\"Il17rd\"]", "do": null }, { "gene_id": 171469, "description": "G protein-coupled receptor 37-like 1", "gene_symbol": "[\"Gpr37l1\"]", "do": null }, { "gene_id": 171486, "description": "CD99 antigen-like 2", "gene_symbol": "[\"Cd99l2\"]", "do": null }, { "gene_id": 171508, "description": "cysteine-rich with EGF-like domains 1", "gene_symbol": "[\"Creld1\"]", "do": null }, { "gene_id": 171580, "description": "microtubule associated monooxygenase, calponin and LIM domain containing 1", "gene_symbol": "[\"Mical1\"]", "do": null }, { "gene_id": 192159, "description": "pre-mRNA processing factor 8", "gene_symbol": "[\"Prpf8\"]", "do": "[{\"label\":\"retinitis pigmentosa 13\",\"id\":\"DOID:0110403\"}]" }, { "gene_id": 192160, "description": "exon junction complex subunit", "gene_symbol": "[\"Casc3\"]", "do": null }, { "gene_id": 192161, "description": "protocadherin alpha 9", "gene_symbol": "[\"Pcdha9\"]", "do": null }, { "gene_id": 192167, "description": "neuroligin 1", "gene_symbol": "[\"Nlgn1\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 192170, "description": "eukaryotic translation initiation factor 4A3", "gene_symbol": "[\"Eif4a3\"]", "do": null }, { "gene_id": 192176, "description": "filamin, alpha", "gene_symbol": "[\"Flna\"]", "do": null }, { "gene_id": 192187, "description": "stabilin 1", "gene_symbol": "[\"Stab1\"]", "do": null }, { "gene_id": 192188, "description": "stabilin 2", "gene_symbol": "[\"Stab2\"]", "do": null }, { "gene_id": 192190, "description": "polycystic kidney and hepatic disease 1-like 1", "gene_symbol": "[\"Pkhd1l1\"]", "do": null }, { "gene_id": 192193, "description": "ER degradation enhancer, mannosidase alpha-like 1", "gene_symbol": "[\"Edem1\"]", "do": null }, { "gene_id": 192194, "description": "butyrophilin-like 10", "gene_symbol": "[\"Btnl10\"]", "do": null }, { "gene_id": 192195, "description": "ASH1 like histone lysine methyltransferase", "gene_symbol": "[\"Ash1l\"]", "do": null }, { "gene_id": 192197, "description": "BCAS3 microtubule associated cell migration factor", "gene_symbol": "[\"Bcas3\"]", "do": null }, { "gene_id": 192198, "description": "leucine rich repeat containing 4", "gene_symbol": "[\"Lrrc4\"]", "do": null }, { "gene_id": 192199, "description": "R-spondin 1", "gene_symbol": "[\"Rspo1\"]", "do": null }, { "gene_id": 192212, "description": "prominin 2", "gene_symbol": "[\"Prom2\"]", "do": null }, { "gene_id": 192285, "description": "PHD finger protein 21A", "gene_symbol": "[\"Phf21a\"]", "do": null }, { "gene_id": 192292, "description": "nuclear receptor binding protein 1", "gene_symbol": "[\"Nrbp1\"]", "do": null }, { "gene_id": 192654, "description": "phospholipase A2, group XV", "gene_symbol": "[\"Pla2g15\"]", "do": null }, { "gene_id": 192897, "description": "integrin beta 4", "gene_symbol": "[\"Itgb4\"]", "do": "[{\"label\":\"junctional epidermolysis bullosa non-Herlitz type\",\"id\":\"DOID:0060738\"},{\"label\":\"junctional epidermolysis bullosa with pyloric atresia\",\"id\":\"DOID:0060733\"}]" }, { "gene_id": 192950, "description": "NAC alpha domain containing", "gene_symbol": "[\"Nacad\"]", "do": null }, { "gene_id": 193034, "description": "transient receptor potential cation channel, subfamily V, member 1", "gene_symbol": "[\"Trpv1\"]", "do": null }, { "gene_id": 193740, "description": "heat shock protein family A (Hsp70) member 1A", "gene_symbol": "[\"Hspa1a\"]", "do": null }, { "gene_id": 193838, "description": "essential meiotic structure-specific endonuclease subunit 2", "gene_symbol": "[\"Eme2\"]", "do": null }, { "gene_id": 194357, "description": "monooxygenase, DBH-like 2", "gene_symbol": "[\"Moxd2\"]", "do": null }, { "gene_id": 194388, "description": "tet methylcytosine dioxygenase 3", "gene_symbol": "[\"Tet3\"]", "do": null }, { "gene_id": 194401, "description": "microtubule associated monooxygenase, calponin and LIM domain containing 3", "gene_symbol": "[\"Mical3\"]", "do": null }, { "gene_id": 194590, "description": "RALBP1 associated Eps domain containing protein 2", "gene_symbol": "[\"Reps2\"]", "do": null }, { "gene_id": 194597, "description": "transmembrane protease, serine 11a", "gene_symbol": "[\"Tmprss11a\"]", "do": null }, { "gene_id": 194604, "description": "serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 16", "gene_symbol": "[\"Serpina16\"]", "do": null }, { "gene_id": 194974, "description": "Sad1 and UNC84 domain containing 3", "gene_symbol": "[\"Sun3\"]", "do": null }, { "gene_id": 195564, "description": "selection and upkeep of intraepithelial T cells 3", "gene_symbol": "[\"Skint3\"]", "do": null }, { "gene_id": 195646, "description": "heparan sulfate (glucosamine) 3-O-sulfotransferase 2", "gene_symbol": "[\"Hs3st2\"]", "do": null }, { "gene_id": 195733, "description": "grainyhead like transcription factor 1", "gene_symbol": "[\"Grhl1\"]", "do": null }, { "gene_id": 207151, "description": "solute carrier family 22 (organic anion transporter), member 19", "gene_symbol": "[\"Slc22a19\"]", "do": null }, { "gene_id": 207182, "description": "gamma-glutamyltransferase 7", "gene_symbol": "[\"Ggt7\"]", "do": null }, { "gene_id": 207214, "description": "La ribonucleoprotein 4", "gene_symbol": "[\"Larp4\"]", "do": null }, { "gene_id": 207227, "description": "syntaxin binding protein 5-like", "gene_symbol": "[\"Stxbp5l\"]", "do": null }, { "gene_id": 207278, "description": "FCH and double SH3 domains 2", "gene_symbol": "[\"Fchsd2\"]", "do": null }, { "gene_id": 207393, "description": "leucine rich repeat and fibronectin type III, extracellular 2", "gene_symbol": "[\"Elfn2\"]", "do": null }, { "gene_id": 207596, "description": "thrombospondin, type I, domain containing 4", "gene_symbol": "[\"Thsd4\"]", "do": null }, { "gene_id": 207607, "description": "coiled-coil domain containing 40", "gene_symbol": "[\"Ccdc40\"]", "do": null }, { "gene_id": 207615, "description": "WD repeat domain 37", "gene_symbol": "[\"Wdr37\"]", "do": null }, { "gene_id": 207667, "description": "SKI family transcriptional corepressor 1", "gene_symbol": "[\"Skor1\"]", "do": null }, { "gene_id": 207683, "description": "immunoglobulin superfamily, member 11", "gene_symbol": "[\"Igsf11\"]", "do": null }, { "gene_id": 207728, "description": "phosphodiesterase 2A, cGMP-stimulated", "gene_symbol": "[\"Pde2a\"]", "do": null }, { "gene_id": 207742, "description": "ring finger protein 43", "gene_symbol": "[\"Rnf43\"]", "do": null }, { "gene_id": 207777, "description": "TSPO associated protein 1", "gene_symbol": "[\"Tspoap1\"]", "do": null }, { "gene_id": 207781, "description": "C2 calcium-dependent domain containing 2", "gene_symbol": "[\"C2cd2\"]", "do": null }, { "gene_id": 207818, "description": "small cell adhesion glycoprotein", "gene_symbol": "[\"Smagp\"]", "do": null }, { "gene_id": 207819, "description": "BCL2 interacting protein 5", "gene_symbol": "[\"Bnip5\"]", "do": null }, { "gene_id": 207839, "description": "polypeptide N-acetylgalactosaminyltransferase 6", "gene_symbol": "[\"Galnt6\"]", "do": null }, { "gene_id": 207911, "description": "melanin-concentrating hormone receptor 1", "gene_symbol": "[\"Mchr1\"]", "do": null }, { "gene_id": 207932, "description": "URB1 ribosome biogenesis 1 homolog (S. cerevisiae)", "gene_symbol": "[\"Urb1\"]", "do": null }, { "gene_id": 207958, "description": "ALG11 alpha-1,2-mannosyltransferase", "gene_symbol": "[\"Alg11\"]", "do": null }, { "gene_id": 208043, "description": "SET domain containing 1B", "gene_symbol": "[\"Setd1b\"]", "do": null }, { "gene_id": 208098, "description": "pannexin 3", "gene_symbol": "[\"Panx3\"]", "do": null }, { "gene_id": 208104, "description": "MLX interacting protein", "gene_symbol": "[\"Mlxip\"]", "do": null }, { "gene_id": 208146, "description": "YEATS domain containing 2", "gene_symbol": "[\"Yeats2\"]", "do": null }, { "gene_id": 208154, "description": "B and T lymphocyte associated", "gene_symbol": "[\"Btla\"]", "do": null }, { "gene_id": 208158, "description": "MAP6 domain containing 1", "gene_symbol": "[\"Map6d1\"]", "do": null }, { "gene_id": 208171, "description": "transmembrane serine protease 7", "gene_symbol": "[\"Tmprss7\"]", "do": null }, { "gene_id": 208177, "description": "pleckstrin homology like domain, family B, member 2", "gene_symbol": "[\"Phldb2\"]", "do": null }, { "gene_id": 208188, "description": "growth hormone secretagogue receptor", "gene_symbol": "[\"Ghsr\"]", "do": null }, { "gene_id": 208211, "description": "ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase", "gene_symbol": "[\"Alg1\"]", "do": null }, { "gene_id": 208213, "description": "transmembrane protein 132C", "gene_symbol": "[\"Tmem132c\"]", "do": null }, { "gene_id": 208263, "description": "torsin A interacting protein 1", "gene_symbol": "[\"Tor1aip1\"]", "do": null }, { "gene_id": 208266, "description": "DOT1 like histone lysine methyltransferase", "gene_symbol": "[\"Dot1l\"]", "do": "[{\"label\":\"dilated cardiomyopathy 1A\",\"id\":\"DOID:0110425\"}]" }, { "gene_id": 208431, "description": "shroom family member 4", "gene_symbol": "[\"Shroom4\"]", "do": null }, { "gene_id": 208618, "description": "enhancer trap locus 4", "gene_symbol": "[\"Etl4\"]", "do": null }, { "gene_id": 208624, "description": "ALG3 alpha-1,3- mannosyltransferase", "gene_symbol": "[\"Alg3\"]", "do": null }, { "gene_id": 208634, "description": "tetraspanin 10", "gene_symbol": "[\"Tspan10\"]", "do": null }, { "gene_id": 208643, "description": "eukaryotic translation initiation factor 4, gamma 1", "gene_symbol": "[\"Eif4g1\"]", "do": null }, { "gene_id": 208647, "description": "cAMP responsive element binding protein 3-like 2", "gene_symbol": "[\"Creb3l2\"]", "do": null }, { "gene_id": 208659, "description": "FAM20A, golgi associated secretory pathway pseudokinase", "gene_symbol": "[\"Fam20a\"]", "do": null }, { "gene_id": 208677, "description": "cAMP responsive element binding protein 3-like 3", "gene_symbol": "[\"Creb3l3\"]", "do": null }, { "gene_id": 208715, "description": "3-hydroxy-3-methylglutaryl-Coenzyme A synthase 1", "gene_symbol": "[\"Hmgcs1\"]", "do": null }, { "gene_id": 208727, "description": "histone deacetylase 4", "gene_symbol": "[\"Hdac4\"]", "do": "[{\"label\":\"eating disorder\",\"id\":\"DOID:8670\"}]" }, { "gene_id": 208777, "description": "sushi, nidogen and EGF-like domains 1", "gene_symbol": "[\"Sned1\"]", "do": null }, { "gene_id": 208795, "description": "transmembrane protein 63a", "gene_symbol": "[\"Tmem63a\"]", "do": null }, { "gene_id": 208836, "description": "Fanconi anemia, complementation group I", "gene_symbol": "[\"Fanci\"]", "do": null }, { "gene_id": 208846, "description": "dishevelled associated activator of morphogenesis 1", "gene_symbol": "[\"Daam1\"]", "do": "[{\"label\":\"intrinsic cardiomyopathy\",\"id\":\"DOID:0060036\"}]" }, { "gene_id": 208922, "description": "cytoplasmic polyadenylation element binding protein 3", "gene_symbol": "[\"Cpeb3\"]", "do": null }, { "gene_id": 208936, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 18", "gene_symbol": "[\"Adamts18\"]", "do": null }, { "gene_id": 209039, "description": "tensin 2", "gene_symbol": "[\"Tns2\"]", "do": "[{\"label\":\"Pierson syndrome\",\"id\":\"DOID:0060852\"}]" }, { "gene_id": 209268, "description": "immunoglobulin superfamily, member 1", "gene_symbol": "[\"Igsf1\"]", "do": "[{\"label\":\"IGSF1 deficiency syndrome\",\"id\":\"DOID:0111140\"}]" }, { "gene_id": 209357, "description": "general transcription factor IIH, polypeptide 3", "gene_symbol": "[\"Gtf2h3\"]", "do": null }, { "gene_id": 209378, "description": "inter-alpha-trypsin inhibitor, heavy chain 5", "gene_symbol": "[\"Itih5\"]", "do": null }, { "gene_id": 209446, "description": "transcription factor E3", "gene_symbol": "[\"Tfe3\"]", "do": null }, { "gene_id": 209456, "description": "transformation related protein 53 binding protein 2", "gene_symbol": "[\"Trp53bp2\"]", "do": "[{\"label\":\"chromosome 1q41-q42 deletion syndrome\",\"id\":\"DOID:0060412\"}]" }, { "gene_id": 209478, "description": "TBC1D12: TBC1 domain family, member 12", "gene_symbol": "[\"Tbc1d12\"]", "do": null }, { "gene_id": 209512, "description": "trace amine-associated receptor 2", "gene_symbol": "[\"Taar2\"]", "do": null }, { "gene_id": 209513, "description": "trace amine-associated receptor 4", "gene_symbol": "[\"Taar4\"]", "do": null }, { "gene_id": 209517, "description": "trace amine-associated receptor 7B", "gene_symbol": "[\"Taar7b\"]", "do": null }, { "gene_id": 209558, "description": "ectonucleotide pyrophosphatase/phosphodiesterase 3", "gene_symbol": "[\"Enpp3\"]", "do": null }, { "gene_id": 209590, "description": "interleukin 23 receptor", "gene_symbol": "[\"Il23r\"]", "do": null }, { "gene_id": 209630, "description": "FERM domain containing 4A", "gene_symbol": "[\"Frmd4a\"]", "do": null }, { "gene_id": 209683, "description": "tetratricopeptide repeat domain 28", "gene_symbol": "[\"Ttc28\"]", "do": null }, { "gene_id": 209692, "description": "dehydrogenase E1 and transketolase domain containing 1", "gene_symbol": "[\"Dhtkd1\"]", "do": "[{\"label\":\"2-aminoadipic 2-oxoadipic aciduria\",\"id\":\"DOID:0111453\"},{\"label\":\"Charcot-Marie-Tooth disease axonal type 2Q\",\"id\":\"DOID:0110170\"}]" }, { "gene_id": 209743, "description": "membrane integral NOTCH2 associated receptor 1", "gene_symbol": "[\"Minar1\"]", "do": null }, { "gene_id": 209760, "description": "transmembrane channel-like gene family 7", "gene_symbol": "[\"Tmc7\"]", "do": null }, { "gene_id": 209776, "description": "G protein-coupled receptor 139", "gene_symbol": "[\"Gpr139\"]", "do": null }, { "gene_id": 209837, "description": "solute carrier family 38, member 5", "gene_symbol": "[\"Slc38a5\"]", "do": null }, { "gene_id": 210004, "description": "queuosine-tRNA galactosyltransferase", "gene_symbol": "[\"Qtgal\"]", "do": null }, { "gene_id": 210029, "description": "meteorin, glial cell differentiation regulator-like", "gene_symbol": "[\"Metrnl\"]", "do": null }, { "gene_id": 210035, "description": "nuclear envelope integral membrane protein 1", "gene_symbol": "[\"Nemp1\"]", "do": null }, { "gene_id": 210094, "description": "IgLON family member 5", "gene_symbol": "[\"Iglon5\"]", "do": null }, { "gene_id": 210106, "description": "terminal nucleotidyltransferase 4A", "gene_symbol": "[\"Tent4a\"]", "do": null }, { "gene_id": 210108, "description": "RIKEN cDNA D130043K22 gene", "gene_symbol": "[\"D130043K22Rik\"]", "do": null }, { "gene_id": 210126, "description": "LIM domain containing preferred translocation partner in lipoma", "gene_symbol": "[\"Lpp\"]", "do": null }, { "gene_id": 210148, "description": "solute carrier family 30 (zinc transporter), member 6", "gene_symbol": "[\"Slc30a6\"]", "do": null }, { "gene_id": 210172, "description": "zinc finger protein 526", "gene_symbol": "[\"Zfp526\"]", "do": null }, { "gene_id": 210198, "description": "G protein-coupled receptor, family C, group 6, member A", "gene_symbol": "[\"Gprc6a\"]", "do": null }, { "gene_id": 210274, "description": "SH3 and multiple ankyrin repeat domains 2", "gene_symbol": "[\"Shank2\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 210293, "description": "dedicator of cytokinesis 10", "gene_symbol": "[\"Dock10\"]", "do": null }, { "gene_id": 210356, "description": "NCK-associated protein 5", "gene_symbol": "[\"Nckap5\"]", "do": null }, { "gene_id": 210376, "description": "myotubularin related protein 9", "gene_symbol": "[\"Mtmr9\"]", "do": null }, { "gene_id": 210417, "description": "thrombospondin, type I, domain containing 7B", "gene_symbol": "[\"Thsd7b\"]", "do": null }, { "gene_id": 210463, "description": "solute carrier family 22 (organic cation transporter), member 22", "gene_symbol": "[\"Slc22a22\"]", "do": null }, { "gene_id": 210530, "description": "prolyl 3-hydroxylase 2", "gene_symbol": "[\"P3h2\"]", "do": null }, { "gene_id": 210622, "description": "peptidase domain containing associated with muscle regeneration 1", "gene_symbol": "[\"Pamr1\"]", "do": null }, { "gene_id": 210673, "description": "proline-rich transmembrane protein 3", "gene_symbol": "[\"Prrt3\"]", "do": null }, { "gene_id": 210741, "description": "potassium channel, subfamily K, member 12", "gene_symbol": "[\"Kcnk12\"]", "do": null }, { "gene_id": 210789, "description": "TBC1 domain family, member 4", "gene_symbol": "[\"Tbc1d4\"]", "do": null }, { "gene_id": 210801, "description": "unc-5 netrin receptor D", "gene_symbol": "[\"Unc5d\"]", "do": null }, { "gene_id": 210808, "description": "laccase domain containing 1", "gene_symbol": "[\"Lacc1\"]", "do": null }, { "gene_id": 210933, "description": "adhesion G protein-coupled receptor B3", "gene_symbol": "[\"Adgrb3\"]", "do": null }, { "gene_id": 210973, "description": "kelch repeat and BTB (POZ) domain containing 2", "gene_symbol": "[\"Kbtbd2\"]", "do": null }, { "gene_id": 210982, "description": "BRD4 interacting chromatin remodeling complex associated protein like", "gene_symbol": "[\"Bicral\"]", "do": null }, { "gene_id": 210998, "description": "family with sequence similarity 91, member A1", "gene_symbol": "[\"Fam91a1\"]", "do": null }, { "gene_id": 211187, "description": "leucine-rich repeats and transmembrane domains 2", "gene_symbol": "[\"Lrtm2\"]", "do": null }, { "gene_id": 211228, "description": "leucine rich repeat containing 25", "gene_symbol": "[\"Lrrc25\"]", "do": null }, { "gene_id": 211286, "description": "ceroid-lipofuscinosis, neuronal 5", "gene_symbol": "[\"Cln5\"]", "do": "[{\"label\":\"neuronal ceroid lipofuscinosis 5\",\"id\":\"DOID:0110728\"}]" }, { "gene_id": 211401, "description": "MTSS I-BAR domain containing 1", "gene_symbol": "[\"Mtss1\"]", "do": "[{\"label\":\"non-Hodgkin lymphoma\",\"id\":\"DOID:0060060\"}]" }, { "gene_id": 211468, "description": "potassium voltage-gated channel, subfamily H (eag-related), member 8", "gene_symbol": "[\"Kcnh8\"]", "do": null }, { "gene_id": 211488, "description": "2-aminoethanethiol dioxygenase", "gene_symbol": "[\"Ado\"]", "do": null }, { "gene_id": 211499, "description": "transmembrane protein 87A", "gene_symbol": "[\"Tmem87a\"]", "do": null }, { "gene_id": 211548, "description": "nodal modulator 1", "gene_symbol": "[\"Nomo1\"]", "do": null }, { "gene_id": 211577, "description": "MAS-related GPR, member F", "gene_symbol": "[\"Mrgprf\"]", "do": null }, { "gene_id": 211578, "description": "MAS-related GPR, member D", "gene_symbol": "[\"Mrgprd\"]", "do": "[{\"label\":\"dilated cardiomyopathy\",\"id\":\"DOID:12930\"}]" }, { "gene_id": 211612, "description": "patched domain containing 1", "gene_symbol": "[\"Ptchd1\"]", "do": "[{\"label\":\"attention deficit hyperactivity disorder\",\"id\":\"DOID:1094\"}]" }, { "gene_id": 211712, "description": "protocadherin 9", "gene_symbol": "[\"Pcdh9\"]", "do": null }, { "gene_id": 211739, "description": "V-set and transmembrane domain containing 2A", "gene_symbol": "[\"Vstm2a\"]", "do": null }, { "gene_id": 211914, "description": "ArfGAP with SH3 domain, ankyrin repeat and PH domain 2", "gene_symbol": "[\"Asap2\"]", "do": null }, { "gene_id": 211924, "description": "desmoglein 1 gamma", "gene_symbol": "[\"Dsg1c\"]", "do": null }, { "gene_id": 212032, "description": "hexokinase 3", "gene_symbol": "[\"Hk3\"]", "do": null }, { "gene_id": 212070, "description": "clarin 3", "gene_symbol": "[\"Clrn3\"]", "do": null }, { "gene_id": 212114, "description": "NHL repeat containing 3", "gene_symbol": "[\"Nhlrc3\"]", "do": null }, { "gene_id": 212124, "description": "cilia and flagella associated protein 46", "gene_symbol": "[\"Cfap46\"]", "do": null }, { "gene_id": 212127, "description": "proline and serine rich 1", "gene_symbol": "[\"Proser1\"]", "do": null }, { "gene_id": 212139, "description": "coiled-coil and C2 domain containing 1A", "gene_symbol": "[\"Cc2d1a\"]", "do": null }, { "gene_id": 212307, "description": "microtubule-associated protein, RP/EB family, member 2", "gene_symbol": "[\"Mapre2\"]", "do": null }, { "gene_id": 212391, "description": "ligand dependent nuclear receptor corepressor", "gene_symbol": "[\"Lcor\"]", "do": null }, { "gene_id": 212518, "description": "shadow of prion protein", "gene_symbol": "[\"Sprn\"]", "do": null }, { "gene_id": 212528, "description": "tRNA methyltransferase 1", "gene_symbol": "[\"Trmt1\"]", "do": null }, { "gene_id": 212541, "description": "rhodopsin", "gene_symbol": "[\"Rho\"]", "do": "[{\"label\":\"congenital stationary night blindness autosomal dominant 1\",\"id\":\"DOID:0110862\"},{\"label\":\"retinitis pigmentosa 4\",\"id\":\"DOID:0110372\"}]" }, { "gene_id": 212555, "description": "solute carrier family 66 member 1", "gene_symbol": "[\"Slc66a1\"]", "do": null }, { "gene_id": 212728, "description": "TAR RNA binding protein 1", "gene_symbol": "[\"Tarbp1\"]", "do": null }, { "gene_id": 212880, "description": "DEAD box helicase 46", "gene_symbol": "[\"Ddx46\"]", "do": null }, { "gene_id": 212898, "description": "dermatan sulfate epimerase", "gene_symbol": "[\"Dse\"]", "do": null }, { "gene_id": 212933, "description": "peptidase M20 domain containing 1", "gene_symbol": "[\"Pm20d1\"]", "do": null }, { "gene_id": 212974, "description": "protein glucosylgalactosylhydroxylysine glucosidase", "gene_symbol": "[\"Pgghg\"]", "do": null }, { "gene_id": 212996, "description": "polypeptide N-acetylgalactosaminyltransferase 17", "gene_symbol": "[\"Galnt17\"]", "do": null }, { "gene_id": 213006, "description": "major facilitator superfamily domain containing 4A", "gene_symbol": "[\"Mfsd4a\"]", "do": null }, { "gene_id": 213012, "description": "abhydrolase domain containing 10", "gene_symbol": "[\"Abhd10\"]", "do": null }, { "gene_id": 213053, "description": "solute carrier family 39 (zinc transporter), member 14", "gene_symbol": "[\"Slc39a14\"]", "do": null }, { "gene_id": 213056, "description": "hyccin PI4KA lipid kinase complex subunit 2", "gene_symbol": "[\"Hycc2\"]", "do": null }, { "gene_id": 213109, "description": "PHD finger protein 3", "gene_symbol": "[\"Phf3\"]", "do": null }, { "gene_id": 213171, "description": "serine protease 27", "gene_symbol": "[\"Prss27\"]", "do": null }, { "gene_id": 213233, "description": "TAP binding protein-like", "gene_symbol": "[\"Tapbpl\"]", "do": null }, { "gene_id": 213262, "description": "follistatin-like 5", "gene_symbol": "[\"Fstl5\"]", "do": null }, { "gene_id": 213326, "description": "SCY1-like 2 (S. cerevisiae)", "gene_symbol": "[\"Scyl2\"]", "do": null }, { "gene_id": 213332, "description": "major facilitator superfamily domain containing 4B4", "gene_symbol": "[\"Mfsd4b4\"]", "do": null }, { "gene_id": 213350, "description": "glutamine amidotransferase like class 1 domain containing 1", "gene_symbol": "[\"Gatd1\"]", "do": null }, { "gene_id": 213439, "description": "G protein-coupled receptor 174", "gene_symbol": "[\"Gpr174\"]", "do": null }, { "gene_id": 213464, "description": "retinoblastoma binding protein 5, histone lysine methyltransferase complex subunit", "gene_symbol": "[\"Rbbp5\"]", "do": null }, { "gene_id": 213469, "description": "leucine-rich repeat LGI family, member 3", "gene_symbol": "[\"Lgi3\"]", "do": null }, { "gene_id": 213527, "description": "parathyroid hormone 2 receptor", "gene_symbol": "[\"Pth2r\"]", "do": null }, { "gene_id": 213541, "description": "YTH N6-methyladenosine RNA binding protein 2", "gene_symbol": "[\"Ythdf2\"]", "do": null }, { "gene_id": 213556, "description": "pleckstrin homology domain containing, family H (with MyTH4 domain) member 2", "gene_symbol": "[\"Plekhh2\"]", "do": null }, { "gene_id": 213603, "description": "solute carrier family 44, member 3", "gene_symbol": "[\"Slc44a3\"]", "do": null }, { "gene_id": 213673, "description": "RIKEN cDNA 9530068E07 gene", "gene_symbol": "[\"9530068E07Rik\"]", "do": null }, { "gene_id": 213696, "description": "dual oxidase maturation factor 1", "gene_symbol": "[\"Duoxa1\"]", "do": null }, { "gene_id": 213753, "description": "zinc finger protein 598", "gene_symbol": "[\"Zfp598\"]", "do": null }, { "gene_id": 213788, "description": "cholinergic receptor, muscarinic 5", "gene_symbol": "[\"Chrm5\"]", "do": null }, { "gene_id": 213819, "description": "CAS1 domain containing 1", "gene_symbol": "[\"Casd1\"]", "do": null }, { "gene_id": 213988, "description": "trinucleotide repeat containing 6b", "gene_symbol": "[\"Tnrc6b\"]", "do": null }, { "gene_id": 213993, "description": "coiled-coil domain containing 186", "gene_symbol": "[\"Ccdc186\"]", "do": null }, { "gene_id": 214058, "description": "multiple EGF-like-domains 11", "gene_symbol": "[\"Megf11\"]", "do": null }, { "gene_id": 214063, "description": "DnaJ heat shock protein family (Hsp40) member C16", "gene_symbol": "[\"Dnajc16\"]", "do": null }, { "gene_id": 214084, "description": "solute carrier family 18 (vesicular monoamine), member 2", "gene_symbol": "[\"Slc18a2\"]", "do": null }, { "gene_id": 214111, "description": "solute carrier family 24 (sodium/potassium/calcium exchanger), member 1", "gene_symbol": "[\"Slc24a1\"]", "do": "[{\"label\":\"congenital stationary night blindness 1D\",\"id\":\"DOID:0110868\"}]" }, { "gene_id": 214112, "description": "NIPA-like domain containing 4", "gene_symbol": "[\"Nipal4\"]", "do": null }, { "gene_id": 214133, "description": "tet methylcytosine dioxygenase 2", "gene_symbol": "[\"Tet2\"]", "do": null }, { "gene_id": 214240, "description": "dispatched RND transporter family member 2", "gene_symbol": "[\"Disp2\"]", "do": null }, { "gene_id": 214292, "description": "syncytin a", "gene_symbol": "[\"Syna\"]", "do": null }, { "gene_id": 214305, "description": "hedgehog interacting protein-like 1", "gene_symbol": "[\"Hhipl1\"]", "do": null }, { "gene_id": 214321, "description": "predicted gene 4787", "gene_symbol": "[\"Gm4787\"]", "do": null }, { "gene_id": 214403, "description": "complement factor H-related 4", "gene_symbol": "[\"Cfhr4\"]", "do": null }, { "gene_id": 214424, "description": "poly (ADP-ribose) polymerase family, member 16", "gene_symbol": "[\"Parp16\"]", "do": null }, { "gene_id": 214425, "description": "cartilage intermediate layer protein, nucleotide pyrophosphohydrolase", "gene_symbol": "[\"Cilp\"]", "do": null }, { "gene_id": 214469, "description": "family with sequence similarity 168, member B", "gene_symbol": "[\"Fam168b\"]", "do": null }, { "gene_id": 214505, "description": "N-acetylglucosamine-1-phosphotransferase, gamma subunit", "gene_symbol": "[\"Gnptg\"]", "do": null }, { "gene_id": 214523, "description": "transmembrane protease, serine 4", "gene_symbol": "[\"Tmprss4\"]", "do": null }, { "gene_id": 214579, "description": "aldhehyde dehydrogenase family 5, subfamily A1", "gene_symbol": "[\"Aldh5a1\"]", "do": "[{\"label\":\"epilepsy\",\"id\":\"DOID:1826\"}]" }, { "gene_id": 214597, "description": "SID1 transmembrane family, member 2", "gene_symbol": "[\"Sidt2\"]", "do": "[{\"label\":\"metabolic dysfunction-associated steatotic liver disease\",\"id\":\"DOID:0080208\"}]" }, { "gene_id": 214639, "description": "RIKEN cDNA 4930486L24 gene", "gene_symbol": "[\"4930486L24Rik\"]", "do": null }, { "gene_id": 214685, "description": "chondroadherin-like", "gene_symbol": "[\"Chadl\"]", "do": null }, { "gene_id": 214766, "description": "matrix metallopeptidase 21", "gene_symbol": "[\"Mmp21\"]", "do": "[{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 214779, "description": "zinc finger protein 879", "gene_symbol": "[\"Zfp879\"]", "do": null }, { "gene_id": 214812, "description": "zinc finger protein 609", "gene_symbol": "[\"Zfp609\"]", "do": null }, { "gene_id": 214895, "description": "lectin, mannose-binding 2-like", "gene_symbol": "[\"Lman2l\"]", "do": null }, { "gene_id": 214897, "description": "casein kinase 1, gamma 1", "gene_symbol": "[\"Csnk1g1\"]", "do": null }, { "gene_id": 214901, "description": "CTF18, chromosome transmission fidelity factor 18", "gene_symbol": "[\"Chtf18\"]", "do": null }, { "gene_id": 214922, "description": "solute carrier family 39 (zinc transporter), member 2", "gene_symbol": "[\"Slc39a2\"]", "do": null }, { "gene_id": 214931, "description": "F-box and leucine-rich repeat protein 16", "gene_symbol": "[\"Fbxl16\"]", "do": null }, { "gene_id": 214968, "description": "sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D", "gene_symbol": "[\"Sema6d\"]", "do": null }, { "gene_id": 214987, "description": "CTF8, chromosome transmission fidelity factor 8", "gene_symbol": "[\"Chtf8\"]", "do": null }, { "gene_id": 215001, "description": "WAP, FS, Ig, KU, and NTR-containing protein 1", "gene_symbol": "[\"Wfikkn1\"]", "do": null }, { "gene_id": 215015, "description": "FAM20B, glycosaminoglycan xylosylkinase", "gene_symbol": "[\"Fam20b\"]", "do": null }, { "gene_id": 215090, "description": "mannosidase, endo-alpha-like", "gene_symbol": "[\"Maneal\"]", "do": null }, { "gene_id": 215113, "description": "solute carrier family 43, member 2", "gene_symbol": "[\"Slc43a2\"]", "do": null }, { "gene_id": 215335, "description": "solute carrier family 36 (proton/amino acid symporter), member 1", "gene_symbol": "[\"Slc36a1\"]", "do": null }, { "gene_id": 215351, "description": "SUMO/sentrin specific peptidase 6", "gene_symbol": "[\"Senp6\"]", "do": null }, { "gene_id": 215378, "description": "bone morphogenetic protein/retinoic acid inducible neural specific 3", "gene_symbol": "[\"Brinp3\"]", "do": null }, { "gene_id": 215384, "description": "Fc fragment of IgG binding protein", "gene_symbol": "[\"Fcgbp\"]", "do": null }, { "gene_id": 215387, "description": "non-SMC condensin I complex, subunit H", "gene_symbol": "[\"Ncaph\"]", "do": null }, { "gene_id": 215446, "description": "ectonucleoside triphosphate diphosphohydrolase 3", "gene_symbol": "[\"Entpd3\"]", "do": null }, { "gene_id": 215493, "description": "alpha 1,3-galactosyltransferase 2", "gene_symbol": "[\"A3galt2\"]", "do": null }, { "gene_id": 215494, "description": "protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2", "gene_symbol": "[\"Pomgnt2\"]", "do": null }, { "gene_id": 215615, "description": "arginyl aminopeptidase (aminopeptidase B)", "gene_symbol": "[\"Rnpep\"]", "do": null }, { "gene_id": 215654, "description": "cadherin 12", "gene_symbol": "[\"Cdh12\"]", "do": null }, { "gene_id": 215690, "description": "neuron navigator 1", "gene_symbol": "[\"Nav1\"]", "do": null }, { "gene_id": 215751, "description": "glycoprotein integral membrane 1", "gene_symbol": "[\"Ginm1\"]", "do": null }, { "gene_id": 215798, "description": "adhesion G protein-coupled receptor G6", "gene_symbol": "[\"Adgrg6\"]", "do": "[{\"label\":\"idiopathic scoliosis\",\"id\":\"DOID:0060250\"}]" }, { "gene_id": 215814, "description": "coiled-coil domain containing 28A", "gene_symbol": "[\"Ccdc28a\"]", "do": null }, { "gene_id": 215819, "description": "NHS like 1", "gene_symbol": "[\"Nhsl1\"]", "do": null }, { "gene_id": 215821, "description": "ARFGEF family member 3", "gene_symbol": "[\"Arfgef3\"]", "do": null }, { "gene_id": 215854, "description": "trace amine-associated receptor 5", "gene_symbol": "[\"Taar5\"]", "do": null }, { "gene_id": 215855, "description": "trace amine-associated receptor 6", "gene_symbol": "[\"Taar6\"]", "do": null }, { "gene_id": 215856, "description": "trace amine-associated receptor 7A", "gene_symbol": "[\"Taar7a\"]", "do": null }, { "gene_id": 215859, "description": "trace amine-associated receptor 8A", "gene_symbol": "[\"Taar8a\"]", "do": null }, { "gene_id": 215900, "description": "calcium homeostasis modulator family member 6", "gene_symbol": "[\"Calhm6\"]", "do": null }, { "gene_id": 215928, "description": "major facilitator superfamily domain containing 4B5", "gene_symbol": "[\"Mfsd4b5\"]", "do": null }, { "gene_id": 215929, "description": "major facilitator superfamily domain containing 4B1", "gene_symbol": "[\"Mfsd4b1\"]", "do": null }, { "gene_id": 216019, "description": "hexokinase domain containing 1", "gene_symbol": "[\"Hkdc1\"]", "do": null }, { "gene_id": 216021, "description": "storkhead box 1", "gene_symbol": "[\"Stox1\"]", "do": null }, { "gene_id": 216028, "description": "leucine rich repeat transmembrane neuronal 3", "gene_symbol": "[\"Lrrtm3\"]", "do": null }, { "gene_id": 216033, "description": "catenin alpha 3", "gene_symbol": "[\"Ctnna3\"]", "do": null }, { "gene_id": 216131, "description": "trafficking protein particle complex 10", "gene_symbol": "[\"Trappc10\"]", "do": "[{\"label\":\"agnathia-otocephaly complex\",\"id\":\"DOID:0060341\"},{\"label\":\"velocardiofacial syndrome\",\"id\":\"DOID:12583\"}]" }, { "gene_id": 216148, "description": "SHC (Src homology 2 domain containing) transforming protein 2", "gene_symbol": "[\"Shc2\"]", "do": null }, { "gene_id": 216150, "description": "cell division cycle 34", "gene_symbol": "[\"Cdc34\"]", "do": null }, { "gene_id": 216152, "description": "phospholipid phosphatase related 3", "gene_symbol": "[\"Plppr3\"]", "do": null }, { "gene_id": 216157, "description": "transmembrane protein 259", "gene_symbol": "[\"Tmem259\"]", "do": null }, { "gene_id": 216225, "description": "solute carrier family 5 (iodide transporter), member 8", "gene_symbol": "[\"Slc5a8\"]", "do": null }, { "gene_id": 216227, "description": "solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8", "gene_symbol": "[\"Slc17a8\"]", "do": "[{\"label\":\"autosomal dominant nonsyndromic deafness 25\",\"id\":\"DOID:0110555\"}]" }, { "gene_id": 216238, "description": "early endosome antigen 1", "gene_symbol": "[\"Eea1\"]", "do": null }, { "gene_id": 216274, "description": "centrosomal protein 290", "gene_symbol": "[\"Cep290\"]", "do": "[{\"label\":\"Joubert syndrome 5\",\"id\":\"DOID:0111000\"},{\"label\":\"Leber congenital amaurosis 10\",\"id\":\"DOID:0110291\"},{\"label\":\"cystic kidney disease\",\"id\":\"DOID:2975\"},{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 216344, "description": "RAB21, member RAS oncogene family", "gene_symbol": "[\"Rab21\"]", "do": null }, { "gene_id": 216350, "description": "tetraspanin 8", "gene_symbol": "[\"Tspan8\"]", "do": null }, { "gene_id": 216395, "description": "ribitol xylosyltransferase 1", "gene_symbol": "[\"Rxylt1\"]", "do": null }, { "gene_id": 216439, "description": "ArfGAP with GTPase domain, ankyrin repeat and PH domain 2", "gene_symbol": "[\"Agap2\"]", "do": null }, { "gene_id": 216440, "description": "amplified in osteosarcoma", "gene_symbol": "[\"Os9\"]", "do": null }, { "gene_id": 216443, "description": "methionine-tRNA synthetase 1", "gene_symbol": "[\"Mars1\"]", "do": null }, { "gene_id": 216558, "description": "UDP-glucose pyrophosphorylase 2", "gene_symbol": "[\"Ugp2\"]", "do": null }, { "gene_id": 216616, "description": "epidermal growth factor-containing fibulin-like extracellular matrix protein 1", "gene_symbol": "[\"Efemp1\"]", "do": "[{\"label\":\"Doyne honeycomb retinal dystrophy\",\"id\":\"DOID:0060745\"}]" }, { "gene_id": 216618, "description": "cilia and flagella associated protein 36", "gene_symbol": "[\"Cfap36\"]", "do": null }, { "gene_id": 216643, "description": "gamma-aminobutyric acid type A receptor subunit pi", "gene_symbol": "[\"Gabrp\"]", "do": null }, { "gene_id": 216725, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 2", "gene_symbol": "[\"Adamts2\"]", "do": null }, { "gene_id": 216742, "description": "folliculin interacting protein 1", "gene_symbol": "[\"Fnip1\"]", "do": null }, { "gene_id": 216749, "description": "neuromedin U receptor 2", "gene_symbol": "[\"Nmur2\"]", "do": null }, { "gene_id": 216760, "description": "microfibrillar-associated protein 3", "gene_symbol": "[\"Mfap3\"]", "do": null }, { "gene_id": 216766, "description": "gem nuclear organelle associated protein 5", "gene_symbol": "[\"Gemin5\"]", "do": null }, { "gene_id": 216795, "description": "wingless-type MMTV integration site family, member 9A", "gene_symbol": "[\"Wnt9a\"]", "do": null }, { "gene_id": 216797, "description": "serine protease 38", "gene_symbol": "[\"Prss38\"]", "do": null }, { "gene_id": 216810, "description": "target of myb1-like 2 (chicken)", "gene_symbol": "[\"Tom1l2\"]", "do": null }, { "gene_id": 216831, "description": "Rho GTPase activating protein 44", "gene_symbol": "[\"Arhgap44\"]", "do": null }, { "gene_id": 216835, "description": "ubiquitin specific peptidase 43", "gene_symbol": "[\"Usp43\"]", "do": null }, { "gene_id": 216850, "description": "KDM1 lysine (K)-specific demethylase 6B", "gene_symbol": "[\"Kdm6b\"]", "do": null }, { "gene_id": 216856, "description": "neuroligin 2", "gene_symbol": "[\"Nlgn2\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 216864, "description": "macrophage galactose N-acetyl-galactosamine specific lectin 2", "gene_symbol": "[\"Mgl2\"]", "do": null }, { "gene_id": 216871, "description": "glycolipid transfer protein domain containing 2", "gene_symbol": "[\"Gltpd2\"]", "do": null }, { "gene_id": 216873, "description": "sperm associated antigen 7", "gene_symbol": "[\"Spag7\"]", "do": null }, { "gene_id": 216881, "description": "WSC domain containing 1", "gene_symbol": "[\"Wscd1\"]", "do": null }, { "gene_id": 216963, "description": "GIT ArfGAP 1", "gene_symbol": "[\"Git1\"]", "do": "[{\"label\":\"attention deficit hyperactivity disorder\",\"id\":\"DOID:1094\"}]" }, { "gene_id": 216971, "description": "family with sequence similarity 222, member B", "gene_symbol": "[\"Fam222b\"]", "do": null }, { "gene_id": 216984, "description": "ecotropic viral integration site 2b", "gene_symbol": "[\"Evi2b\"]", "do": null }, { "gene_id": 216987, "description": "UTP6 small subunit processome component", "gene_symbol": "[\"Utp6\"]", "do": null }, { "gene_id": 217026, "description": "HEAT repeat containing 6", "gene_symbol": "[\"Heatr6\"]", "do": null }, { "gene_id": 217030, "description": "synergin, gamma", "gene_symbol": "[\"Synrg\"]", "do": null }, { "gene_id": 217039, "description": "gametogenetin binding protein 2", "gene_symbol": "[\"Ggnbp2\"]", "do": null }, { "gene_id": 217109, "description": "UTP18 small subunit processome component", "gene_symbol": "[\"Utp18\"]", "do": null }, { "gene_id": 217116, "description": "spermatogenesis associated 20", "gene_symbol": "[\"Spata20\"]", "do": "[{\"label\":\"oligoasthenoteratozoospermia\",\"id\":\"DOID:0070311\"}]" }, { "gene_id": 217119, "description": "xylosyltransferase II", "gene_symbol": "[\"Xylt2\"]", "do": "[{\"label\":\"polycystic kidney disease\",\"id\":\"DOID:0080322\"}]" }, { "gene_id": 217124, "description": "protein phosphatase 1, regulatory subunit 9B", "gene_symbol": "[\"Ppp1r9b\"]", "do": null }, { "gene_id": 217125, "description": "sterile alpha motif domain containing 14", "gene_symbol": "[\"Samd14\"]", "do": null }, { "gene_id": 217143, "description": "G protein-coupled receptor 179", "gene_symbol": "[\"Gpr179\"]", "do": "[{\"label\":\"congenital stationary night blindness 1E\",\"id\":\"DOID:0110869\"}]" }, { "gene_id": 217166, "description": "nuclear receptor subfamily 1, group D, member 1", "gene_symbol": "[\"Nr1d1\"]", "do": null }, { "gene_id": 217198, "description": "pleckstrin homology domain containing, family H (with MyTH4 domain) member 3", "gene_symbol": "[\"Plekhh3\"]", "do": null }, { "gene_id": 217216, "description": "homologous recombination factor with OB-fold", "gene_symbol": "[\"Hrob\"]", "do": null }, { "gene_id": 217219, "description": "family with sequence similarity 171, member A2", "gene_symbol": "[\"Fam171a2\"]", "do": null }, { "gene_id": 217246, "description": "angiotensin I converting enzyme 3", "gene_symbol": "[\"Ace3\"]", "do": null }, { "gene_id": 217258, "description": "ATP-binding cassette, sub-family A member 8a", "gene_symbol": "[\"Abca8a\"]", "do": null }, { "gene_id": 217262, "description": "ATP-binding cassette, sub-family A member 9", "gene_symbol": "[\"Abca9\"]", "do": null }, { "gene_id": 217265, "description": "ATP-binding cassette, sub-family A member 5", "gene_symbol": "[\"Abca5\"]", "do": null }, { "gene_id": 217302, "description": "G protein-coupled receptor 142", "gene_symbol": "[\"Gpr142\"]", "do": null }, { "gene_id": 217303, "description": "CD300A molecule", "gene_symbol": "[\"Cd300a\"]", "do": null }, { "gene_id": 217304, "description": "CD300 molecule like family member B", "gene_symbol": "[\"Cd300lb\"]", "do": null }, { "gene_id": 217306, "description": "CD300E molecule", "gene_symbol": "[\"Cd300e\"]", "do": null }, { "gene_id": 217342, "description": "ubiquitin-conjugating enzyme E2O", "gene_symbol": "[\"Ube2o\"]", "do": null }, { "gene_id": 217344, "description": "rhomboid 5 homolog 2", "gene_symbol": "[\"Rhbdf2\"]", "do": "[{\"label\":\"palmoplantar keratoderma-esophageal carcinoma syndrome\",\"id\":\"DOID:0111506\"}]" }, { "gene_id": 217351, "description": "trinucleotide repeat containing 6c", "gene_symbol": "[\"Tnrc6c\"]", "do": null }, { "gene_id": 217353, "description": "transmembrane channel-like gene family 6", "gene_symbol": "[\"Tmc6\"]", "do": null }, { "gene_id": 217356, "description": "transmembrane channel-like gene family 8", "gene_symbol": "[\"Tmc8\"]", "do": null }, { "gene_id": 217364, "description": "endo-beta-N-acetylglucosaminidase", "gene_symbol": "[\"Engase\"]", "do": null }, { "gene_id": 217369, "description": "urotensin 2 receptor", "gene_symbol": "[\"Uts2r\"]", "do": null }, { "gene_id": 217653, "description": "MIS18 binding protein 1", "gene_symbol": "[\"Mis18bp1\"]", "do": null }, { "gene_id": 217664, "description": "mannoside acetylglucosaminyltransferase 2", "gene_symbol": "[\"Mgat2\"]", "do": "[{\"label\":\"congenital disorder of glycosylation type IIa\",\"id\":\"DOID:0070253\"}]" }, { "gene_id": 217674, "description": "glycoprotein hormone beta 5", "gene_symbol": "[\"Gphb5\"]", "do": null }, { "gene_id": 217692, "description": "signal-induced proliferation-associated 1 like 1", "gene_symbol": "[\"Sipa1l1\"]", "do": null }, { "gene_id": 217695, "description": "zinc finger, FYVE domain containing 1", "gene_symbol": "[\"Zfyve1\"]", "do": null }, { "gene_id": 217734, "description": "protein-O-mannosyltransferase 2", "gene_symbol": "[\"Pomt2\"]", "do": null }, { "gene_id": 217826, "description": "potassium channel, subfamily K, member 13", "gene_symbol": "[\"Kcnk13\"]", "do": null }, { "gene_id": 217835, "description": "Ras and Rab interactor 3", "gene_symbol": "[\"Rin3\"]", "do": null }, { "gene_id": 217837, "description": "inositol 1,3,4-triphosphate 5/6 kinase", "gene_symbol": "[\"Itpk1\"]", "do": null }, { "gene_id": 217847, "description": "serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10", "gene_symbol": "[\"Serpina10\"]", "do": null }, { "gene_id": 217864, "description": "REST corepressor 1", "gene_symbol": "[\"Rcor1\"]", "do": null }, { "gene_id": 217866, "description": "CDC42 binding protein kinase beta", "gene_symbol": "[\"Cdc42bpb\"]", "do": null }, { "gene_id": 217869, "description": "eukaryotic translation initiation factor 5", "gene_symbol": "[\"Eif5\"]", "do": null }, { "gene_id": 217893, "description": "phosphofurin acidic cluster sorting protein 2", "gene_symbol": "[\"Pacs2\"]", "do": null }, { "gene_id": 217980, "description": "La ribonucleoprotein 4B", "gene_symbol": "[\"Larp4b\"]", "do": null }, { "gene_id": 218038, "description": "amphiphysin", "gene_symbol": "[\"Amph\"]", "do": null }, { "gene_id": 218066, "description": "olfactory receptor family 2 subfamily B member 6", "gene_symbol": "[\"Or2b6\"]", "do": null }, { "gene_id": 218103, "description": "solute carrier family 17 (sodium phosphate), member 2", "gene_symbol": "[\"Slc17a2\"]", "do": null }, { "gene_id": 218194, "description": "phosphatase and actin regulator 1", "gene_symbol": "[\"Phactr1\"]", "do": null }, { "gene_id": 218210, "description": "nucleoporin 153", "gene_symbol": "[\"Nup153\"]", "do": null }, { "gene_id": 218236, "description": "family with sequence similarity 120, member A", "gene_symbol": "[\"Fam120a\"]", "do": null }, { "gene_id": 218271, "description": "beta-1,4-galactosyltransferase 7", "gene_symbol": "[\"B4galt7\"]", "do": null }, { "gene_id": 218335, "description": "CLPTM1-like", "gene_symbol": "[\"Clptm1l\"]", "do": null }, { "gene_id": 218343, "description": "SKI3 subunit of superkiller complex", "gene_symbol": "[\"Skic3\"]", "do": null }, { "gene_id": 218442, "description": "serine incorporator 5", "gene_symbol": "[\"Serinc5\"]", "do": null }, { "gene_id": 218476, "description": "glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase)", "gene_symbol": "[\"Gcnt4\"]", "do": null }, { "gene_id": 218490, "description": "basic transcription factor 3", "gene_symbol": "[\"Btf3\"]", "do": null }, { "gene_id": 218503, "description": "FCH domain only 2", "gene_symbol": "[\"Fcho2\"]", "do": null }, { "gene_id": 218543, "description": "splicing regulatory glutamine/lysine-rich protein 1", "gene_symbol": "[\"Srek1\"]", "do": null }, { "gene_id": 218624, "description": "interleukin 31 receptor A", "gene_symbol": "[\"Il31ra\"]", "do": null }, { "gene_id": 218629, "description": "DExH-box helicase 29", "gene_symbol": "[\"Dhx29\"]", "do": null }, { "gene_id": 218699, "description": "PX domain containing serine/threonine kinase", "gene_symbol": "[\"Pxk\"]", "do": null }, { "gene_id": 218763, "description": "leucine rich repeat containing 3B", "gene_symbol": "[\"Lrrc3b\"]", "do": null }, { "gene_id": 218811, "description": "SEC24 homolog C, COPII coat complex component", "gene_symbol": "[\"Sec24c\"]", "do": null }, { "gene_id": 218820, "description": "zinc finger protein 503", "gene_symbol": "[\"Zfp503\"]", "do": null }, { "gene_id": 218850, "description": "transcription activation suppressor", "gene_symbol": "[\"Tasor\"]", "do": null }, { "gene_id": 218877, "description": "sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3G", "gene_symbol": "[\"Sema3g\"]", "do": null }, { "gene_id": 218914, "description": "WAPL cohesin release factor", "gene_symbol": "[\"Wapl\"]", "do": null }, { "gene_id": 218952, "description": "fermitin family member 2", "gene_symbol": "[\"Fermt2\"]", "do": null }, { "gene_id": 218973, "description": "WD repeat and HMG-box DNA binding protein 1", "gene_symbol": "[\"Wdhd1\"]", "do": null }, { "gene_id": 218975, "description": "mitogen-activated protein kinase 1 interacting protein 1-like", "gene_symbol": "[\"Mapk1ip1l\"]", "do": null }, { "gene_id": 218989, "description": "transmembrane protein 260", "gene_symbol": "[\"Tmem260\"]", "do": null }, { "gene_id": 219134, "description": "shisa family member 2", "gene_symbol": "[\"Shisa2\"]", "do": null }, { "gene_id": 219151, "description": "scavenger receptor class A, member 3", "gene_symbol": "[\"Scara3\"]", "do": null }, { "gene_id": 219158, "description": "cell cycle activator and apoptosis regulator 2", "gene_symbol": "[\"Ccar2\"]", "do": null }, { "gene_id": 219181, "description": "A kinase anchor protein 11", "gene_symbol": "[\"Akap11\"]", "do": null }, { "gene_id": 219189, "description": "von Willebrand factor A domain containing 8", "gene_symbol": "[\"Vwa8\"]", "do": null }, { "gene_id": 219228, "description": "protocadherin 17", "gene_symbol": "[\"Pcdh17\"]", "do": null }, { "gene_id": 219257, "description": "protocadherin 20", "gene_symbol": "[\"Pcdh20\"]", "do": null }, { "gene_id": 223254, "description": "FERM, ARH/RhoGEF and pleckstrin domain protein 1", "gene_symbol": "[\"Farp1\"]", "do": null }, { "gene_id": 223272, "description": "integrin, beta-like 1", "gene_symbol": "[\"Itgbl1\"]", "do": null }, { "gene_id": 223337, "description": "UDP glycosyltransferases 3 family, polypeptide A1", "gene_symbol": "[\"Ugt3a1\"]", "do": null }, { "gene_id": 223435, "description": "triple functional domain (PTPRF interacting)", "gene_symbol": "[\"Trio\"]", "do": null }, { "gene_id": 223473, "description": "NIPA-like domain containing 2", "gene_symbol": "[\"Nipal2\"]", "do": null }, { "gene_id": 223601, "description": "CYFIP related Rac1 interactor B", "gene_symbol": "[\"Cyrib\"]", "do": null }, { "gene_id": 223604, "description": "potassium channel, subfamily K, member 9", "gene_symbol": "[\"Kcnk9\"]", "do": null }, { "gene_id": 223626, "description": "thioesterase superfamily member 6", "gene_symbol": "[\"Them6\"]", "do": null }, { "gene_id": 223650, "description": "epiplakin 1", "gene_symbol": "[\"Eppk1\"]", "do": null }, { "gene_id": 223666, "description": "Rho GTPase activating protein 39", "gene_symbol": "[\"Arhgap39\"]", "do": null }, { "gene_id": 223697, "description": "Sad1 and UNC84 domain containing 2", "gene_symbol": "[\"Sun2\"]", "do": null }, { "gene_id": 223701, "description": "myocardin related transcription factor A", "gene_symbol": "[\"Mrtfa\"]", "do": null }, { "gene_id": 223722, "description": "malonyl CoA:ACP acyltransferase (mitochondrial)", "gene_symbol": "[\"Mcat\"]", "do": null }, { "gene_id": 223774, "description": "ALG12 alpha-1,6-mannosyltransferase", "gene_symbol": "[\"Alg12\"]", "do": null }, { "gene_id": 223809, "description": "submandibular gland protein C", "gene_symbol": "[\"Smgc\"]", "do": null }, { "gene_id": 223827, "description": "glucoside xylosyltransferase 1", "gene_symbol": "[\"Gxylt1\"]", "do": null }, { "gene_id": 223838, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 20", "gene_symbol": "[\"Adamts20\"]", "do": null }, { "gene_id": 223870, "description": "SUMO1/sentrin specific peptidase 1", "gene_symbol": "[\"Senp1\"]", "do": "[{\"label\":\"type 1 diabetes mellitus\",\"id\":\"DOID:9744\"}]" }, { "gene_id": 223989, "description": "meiosis regulator and mRNA stability 1", "gene_symbol": "[\"Marf1\"]", "do": null }, { "gene_id": 224020, "description": "phosphatidylinositol 4-kinase alpha", "gene_symbol": "[\"Pi4ka\"]", "do": null }, { "gene_id": 224022, "description": "solute carrier family 7 (cationic amino acid transporter, y+ system), member 4", "gene_symbol": "[\"Slc7a4\"]", "do": null }, { "gene_id": 224024, "description": "scavenger receptor class F, member 2", "gene_symbol": "[\"Scarf2\"]", "do": null }, { "gene_id": 224045, "description": "eukaryotic translation initiation factor 2B, subunit 5 epsilon", "gene_symbol": "[\"Eif2b5\"]", "do": "[{\"label\":\"leukoencephalopathy with vanishing white matter\",\"id\":\"DOID:0060868\"}]" }, { "gene_id": 224088, "description": "ATPase type 13A3", "gene_symbol": "[\"Atp13a3\"]", "do": null }, { "gene_id": 224105, "description": "p21 (RAC1) activated kinase 2", "gene_symbol": "[\"Pak2\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 224109, "description": "negative regulator of reactive oxygen species", "gene_symbol": "[\"Nrros\"]", "do": null }, { "gene_id": 224116, "description": "mucin 20", "gene_symbol": "[\"Muc20\"]", "do": null }, { "gene_id": 224129, "description": "adenylate cyclase 5", "gene_symbol": "[\"Adcy5\"]", "do": "[{\"label\":\"Parkinson's disease\",\"id\":\"DOID:14330\"}]" }, { "gene_id": 224132, "description": "solute carrier family 49 member 4", "gene_symbol": "[\"Slc49a4\"]", "do": null }, { "gene_id": 224143, "description": "protein O-glucosyltransferase 1", "gene_symbol": "[\"Poglut1\"]", "do": null }, { "gene_id": 224224, "description": "interphotoreceptor matrix proteoglycan 2", "gene_symbol": "[\"Impg2\"]", "do": "[{\"label\":\"retinitis pigmentosa 56\",\"id\":\"DOID:0110371\"},{\"label\":\"vitelliform macular dystrophy\",\"id\":\"DOID:0050661\"}]" }, { "gene_id": 224250, "description": "claudin domain containing 1", "gene_symbol": "[\"Cldnd1\"]", "do": null }, { "gene_id": 224480, "description": "NADPH oxidase 3", "gene_symbol": "[\"Nox3\"]", "do": null }, { "gene_id": 224624, "description": "Rab40C, member RAS oncogene family", "gene_symbol": "[\"Rab40c\"]", "do": null }, { "gene_id": 224630, "description": "BCL2/adenovirus E1B interacting protein 1", "gene_symbol": "[\"Bnip1\"]", "do": null }, { "gene_id": 224648, "description": "bridge-like lipid transfer protein family member 3A", "gene_symbol": "[\"Bltp3a\"]", "do": null }, { "gene_id": 224661, "description": "solute carrier family 26, member 8", "gene_symbol": "[\"Slc26a8\"]", "do": null }, { "gene_id": 224674, "description": "solute carrier family 37 (glycerol-3-phosphate transporter), member 1", "gene_symbol": "[\"Slc37a1\"]", "do": null }, { "gene_id": 224697, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 10", "gene_symbol": "[\"Adamts10\"]", "do": "[{\"label\":\"Weill-Marchesani syndrome\",\"id\":\"DOID:0050475\"}]" }, { "gene_id": 224727, "description": "BCL2-associated athanogene 6", "gene_symbol": "[\"Bag6\"]", "do": null }, { "gene_id": 224742, "description": "ATP-binding cassette, sub-family F member 1", "gene_symbol": "[\"Abcf1\"]", "do": null }, { "gene_id": 224762, "description": "tripartite motif-containing 31", "gene_symbol": "[\"Trim31\"]", "do": null }, { "gene_id": 224792, "description": "adhesion G protein-coupled receptor F5", "gene_symbol": "[\"Adgrf5\"]", "do": null }, { "gene_id": 224794, "description": "ectonucleotide pyrophosphatase/phosphodiesterase 4", "gene_symbol": "[\"Enpp4\"]", "do": null }, { "gene_id": 224807, "description": "transmembrane protein 63b", "gene_symbol": "[\"Tmem63b\"]", "do": null }, { "gene_id": 224826, "description": "ubiquitin protein ligase E3 component n-recognin 2", "gene_symbol": "[\"Ubr2\"]", "do": null }, { "gene_id": 224840, "description": "triggering receptor expressed on myeloid cells-like 4", "gene_symbol": "[\"Treml4\"]", "do": null }, { "gene_id": 224860, "description": "phospholipase C-like 2", "gene_symbol": "[\"Plcl2\"]", "do": null }, { "gene_id": 224903, "description": "scaffold attachment factor B", "gene_symbol": "[\"Safb\"]", "do": null }, { "gene_id": 224904, "description": "mitochondrial contact site and cristae organizing system subunit 13", "gene_symbol": "[\"Micos13\"]", "do": null }, { "gene_id": 224912, "description": "crumbs family member 3", "gene_symbol": "[\"Crb3\"]", "do": null }, { "gene_id": 224938, "description": "praja ring finger ubiquitin ligase 2", "gene_symbol": "[\"Pja2\"]", "do": null }, { "gene_id": 224997, "description": "DLG associated protein 1", "gene_symbol": "[\"Dlgap1\"]", "do": null }, { "gene_id": 225010, "description": "lysocardiolipin acyltransferase 1", "gene_symbol": "[\"Lclat1\"]", "do": null }, { "gene_id": 225115, "description": "supervillin", "gene_symbol": "[\"Svil\"]", "do": null }, { "gene_id": 225131, "description": "WW domain containing adaptor with coiled-coil", "gene_symbol": "[\"Wac\"]", "do": null }, { "gene_id": 225182, "description": "retinoblastoma binding protein 8, endonuclease", "gene_symbol": "[\"Rbbp8\"]", "do": null }, { "gene_id": 225192, "description": "histamine receptor H4", "gene_symbol": "[\"Hrh4\"]", "do": null }, { "gene_id": 225207, "description": "zinc finger protein 521", "gene_symbol": "[\"Zfp521\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 225256, "description": "desmoglein 1 beta", "gene_symbol": "[\"Dsg1b\"]", "do": null }, { "gene_id": 225288, "description": "formin homology 2 domain containing 3", "gene_symbol": "[\"Fhod3\"]", "do": null }, { "gene_id": 225339, "description": "AMME chromosomal region gene 1-like", "gene_symbol": "[\"Ammecr1l\"]", "do": null }, { "gene_id": 225392, "description": "RELT-like 2", "gene_symbol": "[\"Rell2\"]", "do": null }, { "gene_id": 225432, "description": "RNA binding motif protein 27", "gene_symbol": "[\"Rbm27\"]", "do": null }, { "gene_id": 225583, "description": "membrane integral NOTCH2 associated receptor 2", "gene_symbol": "[\"Minar2\"]", "do": "[{\"label\":\"Parkinson's disease\",\"id\":\"DOID:14330\"}]" }, { "gene_id": 225651, "description": "metallophosphoesterase 1", "gene_symbol": "[\"Mppe1\"]", "do": null }, { "gene_id": 225742, "description": "ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5", "gene_symbol": "[\"St8sia5\"]", "do": null }, { "gene_id": 225825, "description": "CD226 antigen", "gene_symbol": "[\"Cd226\"]", "do": null }, { "gene_id": 225875, "description": "leucine rich repeat and fibronectin type III domain containing 4", "gene_symbol": "[\"Lrfn4\"]", "do": null }, { "gene_id": 225876, "description": "lysine (K)-specific demethylase 2A", "gene_symbol": "[\"Kdm2a\"]", "do": null }, { "gene_id": 225887, "description": "NADH:ubiquinone oxidoreductase core subunit S8", "gene_symbol": "[\"Ndufs8\"]", "do": null }, { "gene_id": 225896, "description": "UBX domain protein 1", "gene_symbol": "[\"Ubxn1\"]", "do": null }, { "gene_id": 225908, "description": "myelin regulatory factor", "gene_symbol": "[\"Myrf\"]", "do": null }, { "gene_id": 225913, "description": "triokinase, FMN cyclase", "gene_symbol": "[\"Tkfc\"]", "do": null }, { "gene_id": 225923, "description": "oocyte secreted protein 3", "gene_symbol": "[\"Oosp3\"]", "do": null }, { "gene_id": 226041, "description": "phosphoglucomutase 5", "gene_symbol": "[\"Pgm5\"]", "do": null }, { "gene_id": 226090, "description": "endoplasmic reticulum metallopeptidase 1", "gene_symbol": "[\"Ermp1\"]", "do": null }, { "gene_id": 226101, "description": "myoferlin", "gene_symbol": "[\"Myof\"]", "do": null }, { "gene_id": 226115, "description": "oligodendrocytic myelin paranodal and inner loop protein", "gene_symbol": "[\"Opalin\"]", "do": null }, { "gene_id": 226144, "description": "ER lipid raft associated 1", "gene_symbol": "[\"Erlin1\"]", "do": null }, { "gene_id": 226169, "description": "peroxisome proliferative activated receptor, gamma, coactivator-related 1", "gene_symbol": "[\"Pprc1\"]", "do": null }, { "gene_id": 226180, "description": "internexin neuronal intermediate filament protein, alpha", "gene_symbol": "[\"Ina\"]", "do": null }, { "gene_id": 226182, "description": "TATA-box binding protein associated factor 5", "gene_symbol": "[\"Taf5\"]", "do": null }, { "gene_id": 226251, "description": "actin-binding LIM protein 1", "gene_symbol": "[\"Ablim1\"]", "do": null }, { "gene_id": 226252, "description": "FHF complex subunit HOOK interacting protein 2A", "gene_symbol": "[\"Fhip2a\"]", "do": null }, { "gene_id": 226255, "description": "attractin like 1", "gene_symbol": "[\"Atrnl1\"]", "do": null }, { "gene_id": 226265, "description": "enolase 4", "gene_symbol": "[\"Eno4\"]", "do": null }, { "gene_id": 226278, "description": "prolactin releasing hormone receptor", "gene_symbol": "[\"Prlhr\"]", "do": null }, { "gene_id": 226304, "description": "neuropeptides B/W receptor 1", "gene_symbol": "[\"Npbwr1\"]", "do": null }, { "gene_id": 226412, "description": "R3H domain containing 1", "gene_symbol": "[\"R3hdm1\"]", "do": null }, { "gene_id": 226419, "description": "dual-specificity tyrosine phosphorylation regulated kinase 3", "gene_symbol": "[\"Dyrk3\"]", "do": null }, { "gene_id": 226438, "description": "immunoglobulin-like and fibronectin type III domain containing 1", "gene_symbol": "[\"Igfn1\"]", "do": null }, { "gene_id": 226442, "description": "zinc finger protein 281", "gene_symbol": "[\"Zfp281\"]", "do": null }, { "gene_id": 226517, "description": "SMG7 nonsense mediated mRNA decay factor", "gene_symbol": "[\"Smg7\"]", "do": null }, { "gene_id": 226519, "description": "laminin, gamma 1", "gene_symbol": "[\"Lamc1\"]", "do": null }, { "gene_id": 226527, "description": "crystallin zeta like 2", "gene_symbol": "[\"Cryzl2\"]", "do": null }, { "gene_id": 226541, "description": "kelch-like 20", "gene_symbol": "[\"Klhl20\"]", "do": null }, { "gene_id": 226551, "description": "SUN domain containing ossification factor", "gene_symbol": "[\"Suco\"]", "do": "[{\"label\":\"osteogenesis imperfecta type 5\",\"id\":\"DOID:0110344\"}]" }, { "gene_id": 226562, "description": "proline-rich coiled-coil 2C", "gene_symbol": "[\"Prrc2c\"]", "do": null }, { "gene_id": 226594, "description": "RCSD domain containing 1", "gene_symbol": "[\"Rcsd1\"]", "do": null }, { "gene_id": 226641, "description": "activating transcription factor 6", "gene_symbol": "[\"Atf6\"]", "do": "[{\"label\":\"achromatopsia 7\",\"id\":\"DOID:0110009\"}]" }, { "gene_id": 226652, "description": "Rho GTPase activating protein 30", "gene_symbol": "[\"Arhgap30\"]", "do": null }, { "gene_id": 226747, "description": "AT hook containing transcription factor 1", "gene_symbol": "[\"Ahctf1\"]", "do": null }, { "gene_id": 226751, "description": "CDC42 binding protein kinase alpha", "gene_symbol": "[\"Cdc42bpa\"]", "do": null }, { "gene_id": 226757, "description": "WD repeat domain 26", "gene_symbol": "[\"Wdr26\"]", "do": null }, { "gene_id": 226778, "description": "MAP/microtubule affinity regulating kinase 1", "gene_symbol": "[\"Mark1\"]", "do": null }, { "gene_id": 226844, "description": "feline leukemia virus subgroup C cellular receptor 1", "gene_symbol": "[\"Flvcr1\"]", "do": "[{\"label\":\"Diamond-Blackfan anemia\",\"id\":\"DOID:1339\"}]" }, { "gene_id": 226866, "description": "somatomedin B and thrombospondin, type 1 domain containing", "gene_symbol": "[\"Sbspon\"]", "do": null }, { "gene_id": 226976, "description": "KAT8 regulatory NSL complex subunit 3", "gene_symbol": "[\"Kansl3\"]", "do": null }, { "gene_id": 226977, "description": "ARP1 actin-related protein 1B, centractin beta", "gene_symbol": "[\"Actr1b\"]", "do": null }, { "gene_id": 226982, "description": "eukaryotic translation initiation factor 5B", "gene_symbol": "[\"Eif5b\"]", "do": null }, { "gene_id": 227059, "description": "solute carrier family 39 (zinc transporter), member 10", "gene_symbol": "[\"Slc39a10\"]", "do": null }, { "gene_id": 227197, "description": "NADH:ubiquinone oxidoreductase core subunit S1", "gene_symbol": "[\"Ndufs1\"]", "do": null }, { "gene_id": 227231, "description": "carbamoyl-phosphate synthetase 1", "gene_symbol": "[\"Cps1\"]", "do": "[{\"label\":\"carbamoyl phosphate synthetase I deficiency disease\",\"id\":\"DOID:9280\"}]" }, { "gene_id": 227288, "description": "C-X-C motif chemokine receptor 1", "gene_symbol": "[\"Cxcr1\"]", "do": null }, { "gene_id": 227289, "description": "G protein-coupled bile acid receptor 1", "gene_symbol": "[\"Gpbar1\"]", "do": null }, { "gene_id": 227325, "description": "delta/notch-like EGF repeat containing", "gene_symbol": "[\"Dner\"]", "do": null }, { "gene_id": 227326, "description": "G protein-coupled receptor 55", "gene_symbol": "[\"Gpr55\"]", "do": null }, { "gene_id": 227327, "description": "UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7", "gene_symbol": "[\"B3gnt7\"]", "do": null }, { "gene_id": 227331, "description": "GRB10 interacting GYF protein 2", "gene_symbol": "[\"Gigyf2\"]", "do": null }, { "gene_id": 227333, "description": "diacylglycerol kinase, delta", "gene_symbol": "[\"Dgkd\"]", "do": "[{\"label\":\"Lennox-Gastaut syndrome\",\"id\":\"DOID:0050561\"}]" }, { "gene_id": 227358, "description": "erythroferrone", "gene_symbol": "[\"Erfe\"]", "do": null }, { "gene_id": 227377, "description": "FERM, RhoGEF and pleckstrin domain protein 2", "gene_symbol": "[\"Farp2\"]", "do": null }, { "gene_id": 227394, "description": "solute carrier organic anion transporter family, member 4C1", "gene_symbol": "[\"Slco4c1\"]", "do": null }, { "gene_id": 227446, "description": "RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing", "gene_symbol": "[\"Relch\"]", "do": null }, { "gene_id": 227541, "description": "calcium/calmodulin-dependent protein kinase ID", "gene_symbol": "[\"Camk1d\"]", "do": null }, { "gene_id": 227545, "description": "proline and serine rich 2", "gene_symbol": "[\"Proser2\"]", "do": null }, { "gene_id": 227613, "description": "tubulin, beta 4B class IVB", "gene_symbol": "[\"Tubb4b\"]", "do": null }, { "gene_id": 227619, "description": "mannosidase, alpha, class 1B, member 1", "gene_symbol": "[\"Man1b1\"]", "do": null }, { "gene_id": 227624, "description": "RAB, member RAS oncogene family-like 6", "gene_symbol": "[\"Rabl6\"]", "do": null }, { "gene_id": 227627, "description": "odorant binding protein 2A", "gene_symbol": "[\"Obp2a\"]", "do": null }, { "gene_id": 227632, "description": "potassium channel, subfamily T, member 1", "gene_symbol": "[\"Kcnt1\"]", "do": "[{\"label\":\"developmental and epileptic encephalopathy 14\",\"id\":\"DOID:0080439\"}]" }, { "gene_id": 227634, "description": "calmodulin regulated spectrin-associated protein 1", "gene_symbol": "[\"Camsap1\"]", "do": null }, { "gene_id": 227638, "description": "quiescin Q6 sulfhydryl oxidase 2", "gene_symbol": "[\"Qsox2\"]", "do": null }, { "gene_id": 227648, "description": "SEC16 homolog A, endoplasmic reticulum export factor", "gene_symbol": "[\"Sec16a\"]", "do": null }, { "gene_id": 227656, "description": "REX4, 3'-5' exonuclease", "gene_symbol": "[\"Rexo4\"]", "do": null }, { "gene_id": 227659, "description": "solute carrier family 2 (facilitated glucose transporter), member 6", "gene_symbol": "[\"Slc2a6\"]", "do": null }, { "gene_id": 227671, "description": "globoside alpha-1,3-N-acetylgalactosaminyltransferase 1", "gene_symbol": "[\"Gbgt1\"]", "do": null }, { "gene_id": 227699, "description": "nucleoporin 188", "gene_symbol": "[\"Nup188\"]", "do": null }, { "gene_id": 227700, "description": "SH3-domain GRB2-like endophilin B2", "gene_symbol": "[\"Sh3glb2\"]", "do": null }, { "gene_id": 227720, "description": "nucleoporin 214", "gene_symbol": "[\"Nup214\"]", "do": null }, { "gene_id": 227723, "description": "proline-rich coiled-coil 2B", "gene_symbol": "[\"Prrc2b\"]", "do": null }, { "gene_id": 227753, "description": "gelsolin", "gene_symbol": "[\"Gsn\"]", "do": null }, { "gene_id": 227800, "description": "RAB GTPase activating protein 1", "gene_symbol": "[\"Rabgap1\"]", "do": null }, { "gene_id": 227801, "description": "DENN domain containing 1A", "gene_symbol": "[\"Dennd1a\"]", "do": null }, { "gene_id": 227835, "description": "queuosine-tRNA mannosyltransferase", "gene_symbol": "[\"Qtman\"]", "do": null }, { "gene_id": 227867, "description": "enhancer of polycomb homolog 2", "gene_symbol": "[\"Epc2\"]", "do": null }, { "gene_id": 227937, "description": "plakophilin 4", "gene_symbol": "[\"Pkp4\"]", "do": null }, { "gene_id": 228012, "description": "tousled-like kinase 1", "gene_symbol": "[\"Tlk1\"]", "do": null }, { "gene_id": 228026, "description": "pyruvate dehydrogenase kinase, isoenzyme 1", "gene_symbol": "[\"Pdk1\"]", "do": null }, { "gene_id": 228071, "description": "SEC14 and spectrin domains 1", "gene_symbol": "[\"Sestd1\"]", "do": null }, { "gene_id": 228136, "description": "zinc finger, DHHC domain containing 5", "gene_symbol": "[\"Zdhhc5\"]", "do": null }, { "gene_id": 228139, "description": "purinergic receptor P2X, ligand-gated ion channel, 3", "gene_symbol": "[\"P2rx3\"]", "do": null }, { "gene_id": 228140, "description": "CCR4-NOT transcription complex subunit 12", "gene_symbol": "[\"Cnot12\"]", "do": null }, { "gene_id": 228228, "description": "olfactory receptor family 5 subfamily T member 17", "gene_symbol": "[\"Or5t17\"]", "do": null }, { "gene_id": 228355, "description": "MAP-kinase activating death domain", "gene_symbol": "[\"Madd\"]", "do": "[{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 228356, "description": "centriolar satellite-associated tubulin polyglutamylase complex regulator 1", "gene_symbol": "[\"Cstpp1\"]", "do": null }, { "gene_id": 228357, "description": "low density lipoprotein receptor-related protein 4", "gene_symbol": "[\"Lrp4\"]", "do": "[{\"label\":\"sclerosteosis 2\",\"id\":\"DOID:0060757\"}]" }, { "gene_id": 228361, "description": "autophagy/beclin 1 regulator 1", "gene_symbol": "[\"Ambra1\"]", "do": null }, { "gene_id": 228366, "description": "LARGE xylosyl- and glucuronyltransferase 2", "gene_symbol": "[\"Large2\"]", "do": null }, { "gene_id": 228410, "description": "cleavage stimulation factor, 3' pre-RNA, subunit 3", "gene_symbol": "[\"Cstf3\"]", "do": null }, { "gene_id": 228432, "description": "anoctamin 3", "gene_symbol": "[\"Ano3\"]", "do": null }, { "gene_id": 228550, "description": "inositol 1,4,5-trisphosphate 3-kinase A", "gene_symbol": "[\"Itpka\"]", "do": null }, { "gene_id": 228607, "description": "mitochondrial antiviral signaling protein", "gene_symbol": "[\"Mavs\"]", "do": null }, { "gene_id": 228684, "description": "sel-1 suppressor of lin-12-like 2 (C. elegans)", "gene_symbol": "[\"Sel1l2\"]", "do": null }, { "gene_id": 228714, "description": "lysine acetyltransferase 14", "gene_symbol": "[\"Kat14\"]", "do": null }, { "gene_id": 228756, "description": "cystatin-like 1", "gene_symbol": "[\"Cstl1\"]", "do": null }, { "gene_id": 228770, "description": "R-spondin 4", "gene_symbol": "[\"Rspo4\"]", "do": null }, { "gene_id": 228790, "description": "ASXL transcriptional regulator 1", "gene_symbol": "[\"Asxl1\"]", "do": "[{\"label\":\"acute myeloid leukemia\",\"id\":\"DOID:9119\"},{\"label\":\"myelodysplastic syndrome\",\"id\":\"DOID:0050908\"},{\"label\":\"myeloproliferative neoplasm\",\"id\":\"DOID:2226\"}]" }, { "gene_id": 228796, "description": "BPI fold containing family B, member 6", "gene_symbol": "[\"Bpifb6\"]", "do": null }, { "gene_id": 228801, "description": "BPI fold containing family B, member 1", "gene_symbol": "[\"Bpifb1\"]", "do": null }, { "gene_id": 228836, "description": "DLG associated protein 4", "gene_symbol": "[\"Dlgap4\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 228852, "description": "protein phosphatase 1, regulatory subunit 16B", "gene_symbol": "[\"Ppp1r16b\"]", "do": null }, { "gene_id": 228866, "description": "phosphorylated CTD interacting factor 1", "gene_symbol": "[\"Pcif1\"]", "do": null }, { "gene_id": 228869, "description": "nuclear receptor coactivator 5", "gene_symbol": "[\"Ncoa5\"]", "do": null }, { "gene_id": 228875, "description": "solute carrier family 35 member H1", "gene_symbol": "[\"Slc35h1\"]", "do": null }, { "gene_id": 228880, "description": "zinc finger, MYND-type containing 8", "gene_symbol": "[\"Zmynd8\"]", "do": null }, { "gene_id": 228911, "description": "teashirt zinc finger family member 2", "gene_symbol": "[\"Tshz2\"]", "do": null }, { "gene_id": 228942, "description": "cerebellin 4 precursor protein", "gene_symbol": "[\"Cbln4\"]", "do": null }, { "gene_id": 228980, "description": "TATA-box binding protein associated factor 4", "gene_symbol": "[\"Taf4\"]", "do": null }, { "gene_id": 228994, "description": "YTH N6-methyladenosine RNA binding protein 1", "gene_symbol": "[\"Ythdf1\"]", "do": null }, { "gene_id": 228998, "description": "ARF GTPase activating protein 1", "gene_symbol": "[\"Arfgap1\"]", "do": null }, { "gene_id": 229004, "description": "glucocorticoid modulatory element binding protein 2", "gene_symbol": "[\"Gmeb2\"]", "do": null }, { "gene_id": 229096, "description": "YTH N6-methyladenosine RNA binding protein 3", "gene_symbol": "[\"Ythdf3\"]", "do": null }, { "gene_id": 229211, "description": "acyl-Coenzyme A dehydrogenase family, member 9", "gene_symbol": "[\"Acad9\"]", "do": "[{\"label\":\"nuclear type mitochondrial complex I deficiency 20\",\"id\":\"DOID:0112072\"}]" }, { "gene_id": 229214, "description": "pyroglutamylated RFamide peptide receptor", "gene_symbol": "[\"Qrfpr\"]", "do": "[{\"label\":\"bone structure disease\",\"id\":\"DOID:0080010\"}]" }, { "gene_id": 229227, "description": "bridge-like lipid transfer protein family member 1", "gene_symbol": "[\"Bltp1\"]", "do": null }, { "gene_id": 229279, "description": "heterogeneous nuclear ribonucleoprotein A3", "gene_symbol": "[\"Hnrnpa3\"]", "do": null }, { "gene_id": 229285, "description": "spartin", "gene_symbol": "[\"Spart\"]", "do": "[{\"label\":\"Troyer syndrome\",\"id\":\"DOID:0050886\"}]" }, { "gene_id": 229302, "description": "transmembrane 4 superfamily member 4", "gene_symbol": "[\"Tm4sf4\"]", "do": null }, { "gene_id": 229317, "description": "eukaryotic translation initiation factor 2A", "gene_symbol": "[\"Eif2a\"]", "do": null }, { "gene_id": 229320, "description": "clarin 1", "gene_symbol": "[\"Clrn1\"]", "do": "[{\"label\":\"Usher syndrome type 3\",\"id\":\"DOID:0110828\"},{\"label\":\"Usher syndrome type 3A\",\"id\":\"DOID:0110841\"}]" }, { "gene_id": 229323, "description": "G protein-coupled receptor 171", "gene_symbol": "[\"Gpr171\"]", "do": null }, { "gene_id": 229357, "description": "G protein-coupled receptor 149", "gene_symbol": "[\"Gpr149\"]", "do": null }, { "gene_id": 229363, "description": "guanine monophosphate synthetase", "gene_symbol": "[\"Gmps\"]", "do": null }, { "gene_id": 229389, "description": "otolin 1", "gene_symbol": "[\"Otol1\"]", "do": null }, { "gene_id": 229445, "description": "cathepsin O", "gene_symbol": "[\"Ctso\"]", "do": null }, { "gene_id": 229473, "description": "transmembrane 131 like", "gene_symbol": "[\"Tmem131l\"]", "do": null }, { "gene_id": 229499, "description": "Fc receptor-like 1", "gene_symbol": "[\"Fcrl1\"]", "do": null }, { "gene_id": 229534, "description": "pre B cell leukemia transcription factor interacting protein 1", "gene_symbol": "[\"Pbxip1\"]", "do": null }, { "gene_id": 229542, "description": "GATA zinc finger domain containing 2B", "gene_symbol": "[\"Gatad2b\"]", "do": "[{\"label\":\"GAND syndrome\",\"id\":\"DOID:0070048\"}]" }, { "gene_id": 229574, "description": "filaggrin family member 2", "gene_symbol": "[\"Flg2\"]", "do": null }, { "gene_id": 229584, "description": "pogo transposable element with ZNF domain", "gene_symbol": "[\"Pogz\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 229589, "description": "prune exopolyphosphatase", "gene_symbol": "[\"Prune1\"]", "do": null }, { "gene_id": 229595, "description": "ADAMTS-like 4", "gene_symbol": "[\"Adamtsl4\"]", "do": "[{\"label\":\"autosomal recessive isolated ectopia lentis 2\",\"id\":\"DOID:0111149\"},{\"label\":\"lens disease\",\"id\":\"DOID:110\"}]" }, { "gene_id": 229599, "description": "circadian associated repressor of transcription", "gene_symbol": "[\"Ciart\"]", "do": null }, { "gene_id": 229600, "description": "cDNA sequence BC028528", "gene_symbol": "[\"BC028528\"]", "do": null }, { "gene_id": 229603, "description": "OTU domain containing 7B", "gene_symbol": "[\"Otud7b\"]", "do": null }, { "gene_id": 229615, "description": "protein inhibitor of activated STAT 3", "gene_symbol": "[\"Pias3\"]", "do": null }, { "gene_id": 229663, "description": "cold shock domain containing E1, RNA binding", "gene_symbol": "[\"Csde1\"]", "do": null }, { "gene_id": 229706, "description": "solute carrier family 6 (neurotransmitter transporter), member 17", "gene_symbol": "[\"Slc6a17\"]", "do": null }, { "gene_id": 229714, "description": "G protein-coupled receptor 61", "gene_symbol": "[\"Gpr61\"]", "do": null }, { "gene_id": 229715, "description": "adhesion molecule with Ig like domain 1", "gene_symbol": "[\"Amigo1\"]", "do": null }, { "gene_id": 229722, "description": "endosome-lysosome associated apoptosis and autophagy regulator 1", "gene_symbol": "[\"Elapor1\"]", "do": null }, { "gene_id": 229759, "description": "olfactomedin 3", "gene_symbol": "[\"Olfm3\"]", "do": null }, { "gene_id": 229791, "description": "phospholipid phosphatase related 4", "gene_symbol": "[\"Plppr4\"]", "do": null }, { "gene_id": 229841, "description": "centromere protein E", "gene_symbol": "[\"Cenpe\"]", "do": null }, { "gene_id": 229927, "description": "chloride channel accessory 3B", "gene_symbol": "[\"Clca3b\"]", "do": null }, { "gene_id": 229933, "description": "chloride channel accessory 2", "gene_symbol": "[\"Clca2\"]", "do": null }, { "gene_id": 230027, "description": "coenzyme Q3 methyltransferase", "gene_symbol": "[\"Coq3\"]", "do": null }, { "gene_id": 230085, "description": "PHD finger protein 24", "gene_symbol": "[\"Phf24\"]", "do": null }, { "gene_id": 230088, "description": "atos homolog B", "gene_symbol": "[\"Atosb\"]", "do": null }, { "gene_id": 230099, "description": "carbonic anhydrase 9", "gene_symbol": "[\"Car9\"]", "do": null }, { "gene_id": 230101, "description": "glucosidase beta 2", "gene_symbol": "[\"Gba2\"]", "do": null }, { "gene_id": 230103, "description": "natriuretic peptide receptor 2", "gene_symbol": "[\"Npr2\"]", "do": "[{\"label\":\"achondroplasia\",\"id\":\"DOID:4480\"},{\"label\":\"acromesomelic dysplasia, Maroteaux type\",\"id\":\"DOID:0080050\"},{\"label\":\"bone development disease\",\"id\":\"DOID:0080006\"}]" }, { "gene_id": 230145, "description": "polypeptide N-acetylgalactosaminyltransferase 12", "gene_symbol": "[\"Galnt12\"]", "do": null }, { "gene_id": 230157, "description": "transmembrane protein with EGF-like and two follistatin-like domains 1", "gene_symbol": "[\"Tmeff1\"]", "do": null }, { "gene_id": 230163, "description": "aldolase B, fructose-bisphosphate", "gene_symbol": "[\"Aldob\"]", "do": null }, { "gene_id": 230233, "description": "elongator complex protein 1", "gene_symbol": "[\"Elp1\"]", "do": "[{\"label\":\"familial dysautonomia\",\"id\":\"DOID:11589\"},{\"label\":\"hemophagocytic lymphohistiocytosis\",\"id\":\"DOID:0050120\"}]" }, { "gene_id": 230235, "description": "ferric-chelate reductase 1 like", "gene_symbol": "[\"Frrs1l\"]", "do": null }, { "gene_id": 230249, "description": "Ecm29 proteasome adaptor and scaffold", "gene_symbol": "[\"Ecpas\"]", "do": null }, { "gene_id": 230316, "description": "multiple EGF-like-domains 9", "gene_symbol": "[\"Megf9\"]", "do": null }, { "gene_id": 230379, "description": "alkaline ceramidase 2", "gene_symbol": "[\"Acer2\"]", "do": null }, { "gene_id": 230396, "description": "interferon alpha 13", "gene_symbol": "[\"Ifna13\"]", "do": null }, { "gene_id": 230398, "description": "interferon alpha 16", "gene_symbol": "[\"Ifna16\"]", "do": null }, { "gene_id": 230558, "description": "complement component 8, alpha polypeptide", "gene_symbol": "[\"C8a\"]", "do": null }, { "gene_id": 230579, "description": "family with sequence simliarity 151, member A", "gene_symbol": "[\"Fam151a\"]", "do": null }, { "gene_id": 230584, "description": "Yip1 domain family, member 1", "gene_symbol": "[\"Yipf1\"]", "do": null }, { "gene_id": 230598, "description": "nardilysin convertase", "gene_symbol": "[\"Nrdc\"]", "do": null }, { "gene_id": 230612, "description": "solute carrier family 5 (sodium/glucose cotransporter), member 9", "gene_symbol": "[\"Slc5a9\"]", "do": null }, { "gene_id": 230613, "description": "selection and upkeep of intraepithelial T cells 10", "gene_symbol": "[\"Skint10\"]", "do": null }, { "gene_id": 230622, "description": "selection and upkeep of intraepithelial T cells 6", "gene_symbol": "[\"Skint6\"]", "do": null }, { "gene_id": 230648, "description": "EF-hand calcium binding domain 14", "gene_symbol": "[\"Efcab14\"]", "do": null }, { "gene_id": 230696, "description": "expressed sequence AU022252", "gene_symbol": "[\"AU022252\"]", "do": null }, { "gene_id": 230735, "description": "Eph receptor A10", "gene_symbol": "[\"Epha10\"]", "do": null }, { "gene_id": 230737, "description": "guanine nucleotide binding protein nucleolar 2", "gene_symbol": "[\"Gnl2\"]", "do": null }, { "gene_id": 230753, "description": "thyroid hormone receptor associated protein 3", "gene_symbol": "[\"Thrap3\"]", "do": null }, { "gene_id": 230761, "description": "zinc finger protein 362", "gene_symbol": "[\"Zfp362\"]", "do": null }, { "gene_id": 230770, "description": "transmembrane protein 39b", "gene_symbol": "[\"Tmem39b\"]", "do": null }, { "gene_id": 230775, "description": "adhesion G protein-coupled receptor B2", "gene_symbol": "[\"Adgrb2\"]", "do": null }, { "gene_id": 230777, "description": "hypocretin (orexin) receptor 1", "gene_symbol": "[\"Hcrtr1\"]", "do": null }, { "gene_id": 230793, "description": "AT hook, DNA binding motif, containing 1", "gene_symbol": "[\"Ahdc1\"]", "do": "[{\"label\":\"Xia-Gibbs Syndrome\",\"id\":\"DOID:0070055\"}]" }, { "gene_id": 230796, "description": "WD and tetratricopeptide repeats 1", "gene_symbol": "[\"Wdtc1\"]", "do": null }, { "gene_id": 230801, "description": "phosphatidylinositol glycan anchor biosynthesis, class V", "gene_symbol": "[\"Pigv\"]", "do": null }, { "gene_id": 230824, "description": "grainyhead like transcription factor 3", "gene_symbol": "[\"Grhl3\"]", "do": "[{\"label\":\"Van der Woude syndrome\",\"id\":\"DOID:0060239\"}]" }, { "gene_id": 230828, "description": "interleukin 22 receptor, alpha 1", "gene_symbol": "[\"Il22ra1\"]", "do": null }, { "gene_id": 230857, "description": "endothelin converting enzyme 1", "gene_symbol": "[\"Ece1\"]", "do": "[{\"label\":\"double outlet right ventricle\",\"id\":\"DOID:6406\"}]" }, { "gene_id": 230861, "description": "eukaryotic translation initiation factor 4 gamma, 3", "gene_symbol": "[\"Eif4g3\"]", "do": null }, { "gene_id": 230866, "description": "ER membrane protein complex subunit 1", "gene_symbol": "[\"Emc1\"]", "do": null }, { "gene_id": 230868, "description": "immunoglobulin superfamily, member 21", "gene_symbol": "[\"Igsf21\"]", "do": null }, { "gene_id": 230883, "description": "arylacetamide deacetylase like 3", "gene_symbol": "[\"Aadacl3\"]", "do": null }, { "gene_id": 230903, "description": "F-box protein 44", "gene_symbol": "[\"Fbxo44\"]", "do": null }, { "gene_id": 230904, "description": "F-box protein 2", "gene_symbol": "[\"Fbxo2\"]", "do": null }, { "gene_id": 230917, "description": "transmembrane protein 201", "gene_symbol": "[\"Tmem201\"]", "do": null }, { "gene_id": 230979, "description": "tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)", "gene_symbol": "[\"Tnfrsf14\"]", "do": null }, { "gene_id": 230991, "description": "fibronectin type III domain containing 10", "gene_symbol": "[\"Fndc10\"]", "do": null }, { "gene_id": 230996, "description": "RIKEN cDNA 9430015G10 gene", "gene_symbol": "[\"9430015G10Rik\"]", "do": null }, { "gene_id": 231014, "description": "endosome-lysosome associated apoptosis and autophagy regulator family member 2", "gene_symbol": "[\"Elapor2\"]", "do": null }, { "gene_id": 231044, "description": "gastrulation brain homeobox 1", "gene_symbol": "[\"Gbx1\"]", "do": null }, { "gene_id": 231050, "description": "polypeptide N-acetylgalactosaminyltransferase 11", "gene_symbol": "[\"Galnt11\"]", "do": null }, { "gene_id": 231128, "description": "family with sequence homology 193, member A", "gene_symbol": "[\"Fam193a\"]", "do": null }, { "gene_id": 231148, "description": "actin-binding LIM protein 2", "gene_symbol": "[\"Ablim2\"]", "do": null }, { "gene_id": 231238, "description": "sel-1 suppressor of lin-12-like 3 (C. elegans)", "gene_symbol": "[\"Sel1l3\"]", "do": null }, { "gene_id": 231290, "description": "solute carrier family 10 (sodium/bile acid cotransporter family), member 4", "gene_symbol": "[\"Slc10a4\"]", "do": null }, { "gene_id": 231293, "description": "cell wall biogenesis 43 C-terminal homolog", "gene_symbol": "[\"Cwh43\"]", "do": "[{\"label\":\"normal pressure hydrocephalus\",\"id\":\"DOID:1572\"}]" }, { "gene_id": 231296, "description": "leucine rich repeat containing 66", "gene_symbol": "[\"Lrrc66\"]", "do": null }, { "gene_id": 231327, "description": "phosphoribosyl pyrophosphate amidotransferase", "gene_symbol": "[\"Ppat\"]", "do": null }, { "gene_id": 231329, "description": "polymerase (RNA) II (DNA directed) polypeptide B", "gene_symbol": "[\"Polr2b\"]", "do": null }, { "gene_id": 231380, "description": "ubiquitin-like modifier activating enzyme 6", "gene_symbol": "[\"Uba6\"]", "do": null }, { "gene_id": 231396, "description": "UDP glucuronosyltransferase 2 family, polypeptide B36", "gene_symbol": "[\"Ugt2b36\"]", "do": null }, { "gene_id": 231440, "description": "prostate androgen-regulated mucin-like protein 1", "gene_symbol": "[\"Parm1\"]", "do": null }, { "gene_id": 231452, "description": "SDA1 domain containing 1", "gene_symbol": "[\"Sdad1\"]", "do": null }, { "gene_id": 231470, "description": "Fraser extracellular matrix complex subunit 1", "gene_symbol": "[\"Fras1\"]", "do": "[{\"label\":\"Fraser syndrome\",\"id\":\"DOID:0090001\"},{\"label\":\"clubfoot\",\"id\":\"DOID:11836\"}]" }, { "gene_id": 231506, "description": "lin-54 DREAM MuvB core complex component", "gene_symbol": "[\"Lin54\"]", "do": null }, { "gene_id": 231532, "description": "Rho GTPase activating protein 24", "gene_symbol": "[\"Arhgap24\"]", "do": null }, { "gene_id": 231571, "description": "RNA polymerase II associated protein 2", "gene_symbol": "[\"Rpap2\"]", "do": null }, { "gene_id": 231580, "description": "cyclin G associated kinase", "gene_symbol": "[\"Gak\"]", "do": null }, { "gene_id": 231583, "description": "solute carrier family 26 (sulfate transporter), member 1", "gene_symbol": "[\"Slc26a1\"]", "do": null }, { "gene_id": 231602, "description": "purinergic receptor P2X, ligand-gated ion channel, 2", "gene_symbol": "[\"P2rx2\"]", "do": "[{\"label\":\"autosomal dominant nonsyndromic deafness 41\",\"id\":\"DOID:0110567\"}]" }, { "gene_id": 231605, "description": "polypeptide N-acetylgalactosaminyltransferase 9", "gene_symbol": "[\"Galnt9\"]", "do": null }, { "gene_id": 231630, "description": "FIC domain containing", "gene_symbol": "[\"Ficd\"]", "do": null }, { "gene_id": 231633, "description": "transmembrane protein 119", "gene_symbol": "[\"Tmem119\"]", "do": null }, { "gene_id": 231659, "description": "GCN1 activator of EIF2AK4", "gene_symbol": "[\"Gcn1\"]", "do": null }, { "gene_id": 231668, "description": "V-set and immunoglobulin domain containing 10", "gene_symbol": "[\"Vsig10\"]", "do": null }, { "gene_id": 231691, "description": "serine dehydratase", "gene_symbol": "[\"Sds\"]", "do": null }, { "gene_id": 231724, "description": "RAD9 checkpoint clamp component B", "gene_symbol": "[\"Rad9b\"]", "do": null }, { "gene_id": 231727, "description": "UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 4", "gene_symbol": "[\"B3gnt4\"]", "do": null }, { "gene_id": 231760, "description": "RIMS binding protein 2", "gene_symbol": "[\"Rimbp2\"]", "do": null }, { "gene_id": 231769, "description": "splicing factor SWAP", "gene_symbol": "[\"Sfswap\"]", "do": null }, { "gene_id": 231801, "description": "ArfGAP with FG repeats 2", "gene_symbol": "[\"Agfg2\"]", "do": null }, { "gene_id": 231803, "description": "methylphosphate capping enzyme", "gene_symbol": "[\"Mepce\"]", "do": null }, { "gene_id": 231805, "description": "paired immunoglobin-like type 2 receptor alpha", "gene_symbol": "[\"Pilra\"]", "do": null }, { "gene_id": 231830, "description": "MICAL-like 2", "gene_symbol": "[\"Micall2\"]", "do": null }, { "gene_id": 231832, "description": "transmembrane protein 184a", "gene_symbol": "[\"Tmem184a\"]", "do": null }, { "gene_id": 231841, "description": "BRCA1-associated ATM activator 1", "gene_symbol": "[\"Brat1\"]", "do": null }, { "gene_id": 231861, "description": "trinucleotide repeat containing 18", "gene_symbol": "[\"Tnrc18\"]", "do": null }, { "gene_id": 231946, "description": "family with sequence similarity 221, member A", "gene_symbol": "[\"Fam221a\"]", "do": null }, { "gene_id": 231997, "description": "FK506 binding protein 14", "gene_symbol": "[\"Fkbp14\"]", "do": null }, { "gene_id": 232086, "description": "transmembrane protein 150A", "gene_symbol": "[\"Tmem150a\"]", "do": null }, { "gene_id": 232223, "description": "thioredoxin reductase 3", "gene_symbol": "[\"Txnrd3\"]", "do": null }, { "gene_id": 232227, "description": "IQ motif and Sec7 domain 1", "gene_symbol": "[\"Iqsec1\"]", "do": null }, { "gene_id": 232237, "description": "FYVE, RhoGEF and PH domain containing 5", "gene_symbol": "[\"Fgd5\"]", "do": null }, { "gene_id": 232313, "description": "glucoside xylosyltransferase 2", "gene_symbol": "[\"Gxylt2\"]", "do": null }, { "gene_id": 232314, "description": "protein phosphatase 4, regulatory subunit 2", "gene_symbol": "[\"Ppp4r2\"]", "do": null }, { "gene_id": 232333, "description": "solute carrier family 6 (neurotransmitter transporter, GABA), member 1", "gene_symbol": "[\"Slc6a1\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 232334, "description": "vestigial like family member 4", "gene_symbol": "[\"Vgll4\"]", "do": null }, { "gene_id": 232341, "description": "WNK lysine deficient protein kinase 1", "gene_symbol": "[\"Wnk1\"]", "do": null }, { "gene_id": 232345, "description": "alpha-2-macroglobulin", "gene_symbol": "[\"A2m\"]", "do": null }, { "gene_id": 232370, "description": "calsyntenin 3", "gene_symbol": "[\"Clstn3\"]", "do": null }, { "gene_id": 232371, "description": "complement component 1, r subcomponent-like", "gene_symbol": "[\"C1rl\"]", "do": null }, { "gene_id": 232400, "description": "alpha-2-macroglobulin like 1", "gene_symbol": "[\"A2ml1\"]", "do": null }, { "gene_id": 232408, "description": "killer cell lectin-like receptor subfamily B member 1F", "gene_symbol": "[\"Klrb1f\"]", "do": null }, { "gene_id": 232413, "description": "C-type lectin domain family 12, member a", "gene_symbol": "[\"Clec12a\"]", "do": null }, { "gene_id": 232414, "description": "C-type lectin domain family 9, member a", "gene_symbol": "[\"Clec9a\"]", "do": null }, { "gene_id": 232449, "description": "deoxyribose-phosphate aldolase", "gene_symbol": "[\"Dera\"]", "do": null }, { "gene_id": 232493, "description": "glycogen synthase 2", "gene_symbol": "[\"Gys2\"]", "do": null }, { "gene_id": 232536, "description": "mitochondrial ribosomal protein S35", "gene_symbol": "[\"Mrps35\"]", "do": null }, { "gene_id": 232560, "description": "caprin family member 2", "gene_symbol": "[\"Caprin2\"]", "do": null }, { "gene_id": 232670, "description": "tetraspanin 33", "gene_symbol": "[\"Tspan33\"]", "do": null }, { "gene_id": 232714, "description": "maltase-glucoamylase", "gene_symbol": "[\"Mgam\"]", "do": null }, { "gene_id": 232717, "description": "serine protease 58", "gene_symbol": "[\"Prss58\"]", "do": null }, { "gene_id": 232790, "description": "osteoclast associated receptor", "gene_symbol": "[\"Oscar\"]", "do": null }, { "gene_id": 232798, "description": "leukocyte receptor cluster (LRC) member 8", "gene_symbol": "[\"Leng8\"]", "do": null }, { "gene_id": 232807, "description": "protein phosphatase 1, regulatory subunit 12C", "gene_symbol": "[\"Ppp1r12c\"]", "do": null }, { "gene_id": 232813, "description": "shisa family member 7", "gene_symbol": "[\"Shisa7\"]", "do": null }, { "gene_id": 232906, "description": "Rho GTPase activating protein 35", "gene_symbol": "[\"Arhgap35\"]", "do": null }, { "gene_id": 232944, "description": "MAP/microtubule affinity regulating kinase 4", "gene_symbol": "[\"Mark4\"]", "do": null }, { "gene_id": 232972, "description": "Ly6/PLAUR domain containing 10", "gene_symbol": "[\"Lypd10\"]", "do": null }, { "gene_id": 232973, "description": "Ly6/Plaur domain containing 4", "gene_symbol": "[\"Lypd4\"]", "do": null }, { "gene_id": 232975, "description": "ATPase, Na+/K+ transporting, alpha 3 polypeptide", "gene_symbol": "[\"Atp1a3\"]", "do": "[{\"label\":\"alternating hemiplegia of childhood\",\"id\":\"DOID:0050635\"},{\"label\":\"bipolar disorder\",\"id\":\"DOID:3312\"}]" }, { "gene_id": 232984, "description": "UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8", "gene_symbol": "[\"B3gnt8\"]", "do": null }, { "gene_id": 232989, "description": "heterogeneous nuclear ribonucleoprotein U-like 1", "gene_symbol": "[\"Hnrnpul1\"]", "do": null }, { "gene_id": 233067, "description": "leucine rich repeat and fibronectin type III domain containing 3", "gene_symbol": "[\"Lrfn3\"]", "do": null }, { "gene_id": 233073, "description": "U2 small nuclear RNA auxiliary factor 1-like 4", "gene_symbol": "[\"U2af1l4\"]", "do": null }, { "gene_id": 233079, "description": "free fatty acid receptor 2", "gene_symbol": "[\"Ffar2\"]", "do": null }, { "gene_id": 233080, "description": "free fatty acid receptor 3", "gene_symbol": "[\"Ffar3\"]", "do": null }, { "gene_id": 233081, "description": "free fatty acid receptor 1", "gene_symbol": "[\"Ffar1\"]", "do": null }, { "gene_id": 233115, "description": "dpy-19 like C-mannosyltransferase 3", "gene_symbol": "[\"Dpy19l3\"]", "do": null }, { "gene_id": 233186, "description": "sialic acid binding Ig-like lectin F", "gene_symbol": "[\"Siglecf\"]", "do": null }, { "gene_id": 233187, "description": "lens intrinsic membrane protein 2", "gene_symbol": "[\"Lim2\"]", "do": "[{\"label\":\"cataract 19 multiple types\",\"id\":\"DOID:0110263\"},{\"label\":\"cataract\",\"id\":\"DOID:83\"}]" }, { "gene_id": 233210, "description": "proline rich 12", "gene_symbol": "[\"Prr12\"]", "do": null }, { "gene_id": 233221, "description": "MAS-related GPR, member A1", "gene_symbol": "[\"Mrgpra1\"]", "do": null }, { "gene_id": 233222, "description": "MAS-related GPR, member A3", "gene_symbol": "[\"Mrgpra3\"]", "do": null }, { "gene_id": 233230, "description": "MAS-related GPR, member B4", "gene_symbol": "[\"Mrgprb4\"]", "do": null }, { "gene_id": 233231, "description": "MAS-related GPR, member B1", "gene_symbol": "[\"Mrgprb1\"]", "do": null }, { "gene_id": 233246, "description": "anoctamin 5", "gene_symbol": "[\"Ano5\"]", "do": "[{\"label\":\"autosomal recessive limb-girdle muscular dystrophy type 2L\",\"id\":\"DOID:0110284\"},{\"label\":\"gnathodiaphyseal dysplasia\",\"id\":\"DOID:0111533\"}]" }, { "gene_id": 233271, "description": "leucine zipper protein 2", "gene_symbol": "[\"Luzp2\"]", "do": null }, { "gene_id": 233274, "description": "sialic acid binding Ig-like lectin H", "gene_symbol": "[\"Siglech\"]", "do": null }, { "gene_id": 233424, "description": "transmembrane channel-like gene family 3", "gene_symbol": "[\"Tmc3\"]", "do": null }, { "gene_id": 233489, "description": "phosphatidylinositol binding clathrin assembly protein", "gene_symbol": "[\"Picalm\"]", "do": null }, { "gene_id": 233537, "description": "glycerophosphodiester phosphodiesterase domain containing 4", "gene_symbol": "[\"Gdpd4\"]", "do": null }, { "gene_id": 233545, "description": "EMSY, BRCA2-interacting transcriptional repressor", "gene_symbol": "[\"Emsy\"]", "do": null }, { "gene_id": 233549, "description": "monoacylglycerol O-acyltransferase 2", "gene_symbol": "[\"Mogat2\"]", "do": null }, { "gene_id": 233552, "description": "glycerophosphodiester phosphodiesterase domain containing 5", "gene_symbol": "[\"Gdpd5\"]", "do": null }, { "gene_id": 233571, "description": "pyrimidinergic receptor P2Y, G-protein coupled, 6", "gene_symbol": "[\"P2ry6\"]", "do": null }, { "gene_id": 233651, "description": "dachsous cadherin related 1", "gene_symbol": "[\"Dchs1\"]", "do": "[{\"label\":\"mitral valve prolapse\",\"id\":\"DOID:988\"}]" }, { "gene_id": 233670, "description": "olfactory receptor family 6 subfamily B member 9", "gene_symbol": "[\"Or6b9\"]", "do": null }, { "gene_id": 233733, "description": "polypeptide N-acetylgalactosaminyltransferase 18", "gene_symbol": "[\"Galnt18\"]", "do": null }, { "gene_id": 233744, "description": "spondin 1, (f-spondin) extracellular matrix protein", "gene_symbol": "[\"Spon1\"]", "do": null }, { "gene_id": 233765, "description": "pleckstrin homology domain containing, family A member 7", "gene_symbol": "[\"Plekha7\"]", "do": null }, { "gene_id": 233781, "description": "xylosyltransferase 1", "gene_symbol": "[\"Xylt1\"]", "do": null }, { "gene_id": 233789, "description": "SMG1 nonsense mediated mRNA decay associated PI3K related kinase", "gene_symbol": "[\"Smg1\"]", "do": null }, { "gene_id": 233812, "description": "modulator of smoothened", "gene_symbol": "[\"Mosmo\"]", "do": null }, { "gene_id": 233833, "description": "trinucleotide repeat containing 6a", "gene_symbol": "[\"Tnrc6a\"]", "do": null }, { "gene_id": 233836, "description": "solute carrier family 5 (sodium/glucose cotransporter), member 11", "gene_symbol": "[\"Slc5a11\"]", "do": null }, { "gene_id": 233870, "description": "Tu translation elongation factor, mitochondrial", "gene_symbol": "[\"Tufm\"]", "do": null }, { "gene_id": 233871, "description": "ataxin 2-like", "gene_symbol": "[\"Atxn2l\"]", "do": null }, { "gene_id": 233878, "description": "seizure related 6 homolog like 2", "gene_symbol": "[\"Sez6l2\"]", "do": null }, { "gene_id": 233895, "description": "proline rich 14", "gene_symbol": "[\"Prr14\"]", "do": null }, { "gene_id": 233904, "description": "SET domain containing 1A", "gene_symbol": "[\"Setd1a\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 233908, "description": "fused in sarcoma", "gene_symbol": "[\"Fus\"]", "do": "[{\"label\":\"amyotrophic lateral sclerosis type 6\",\"id\":\"DOID:0060198\"}]" }, { "gene_id": 233979, "description": "two pore segment channel 2", "gene_symbol": "[\"Tpcn2\"]", "do": null }, { "gene_id": 234072, "description": "ADP-ribosylhydrolase like 1", "gene_symbol": "[\"Adprhl1\"]", "do": null }, { "gene_id": 234076, "description": "solute carrier family 9 member D1", "gene_symbol": "[\"Slc9d1\"]", "do": null }, { "gene_id": 234094, "description": "Rho guanine nucleotide exchange factor 10", "gene_symbol": "[\"Arhgef10\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 234135, "description": "nuclear receptor binding SET domain protein 3", "gene_symbol": "[\"Nsd3\"]", "do": null }, { "gene_id": 234199, "description": "fibrinogen-like protein 1", "gene_symbol": "[\"Fgl1\"]", "do": null }, { "gene_id": 234214, "description": "sorbin and SH3 domain containing 2", "gene_symbol": "[\"Sorbs2\"]", "do": null }, { "gene_id": 234258, "description": "nei like 3 (E. coli)", "gene_symbol": "[\"Neil3\"]", "do": null }, { "gene_id": 234267, "description": "glycoprotein m6a", "gene_symbol": "[\"Gpm6a\"]", "do": null }, { "gene_id": 234353, "description": "pleckstrin and Sec7 domain containing 3", "gene_symbol": "[\"Psd3\"]", "do": null }, { "gene_id": 234356, "description": "chondroitin sulfate N-acetylgalactosaminyltransferase 1", "gene_symbol": "[\"Csgalnact1\"]", "do": null }, { "gene_id": 234366, "description": "GATA zinc finger domain containing 2A", "gene_symbol": "[\"Gatad2a\"]", "do": null }, { "gene_id": 234371, "description": "transmembrane protein 161A", "gene_symbol": "[\"Tmem161a\"]", "do": null }, { "gene_id": 234407, "description": "collagen beta(1-O)galactosyltransferase 1", "gene_symbol": "[\"Colgalt1\"]", "do": null }, { "gene_id": 234549, "description": "HEAT repeat containing 3", "gene_symbol": "[\"Heatr3\"]", "do": null }, { "gene_id": 234564, "description": "carboxylesterase 1F", "gene_symbol": "[\"Ces1f\"]", "do": null }, { "gene_id": 234594, "description": "CCR4-NOT transcription complex, subunit 1", "gene_symbol": "[\"Cnot1\"]", "do": null }, { "gene_id": 234664, "description": "NEDD8 activating enzyme E1 subunit 1", "gene_symbol": "[\"Nae1\"]", "do": null }, { "gene_id": 234673, "description": "carboxylesterase 2E", "gene_symbol": "[\"Ces2e\"]", "do": null }, { "gene_id": 234677, "description": "carboxylesterase 4A", "gene_symbol": "[\"Ces4a\"]", "do": null }, { "gene_id": 234686, "description": "formin homology 2 domain containing 1", "gene_symbol": "[\"Fhod1\"]", "do": null }, { "gene_id": 234699, "description": "enhancer of mRNA decapping 4", "gene_symbol": "[\"Edc4\"]", "do": null }, { "gene_id": 234729, "description": "Vac14 homolog (S. cerevisiae)", "gene_symbol": "[\"Vac14\"]", "do": null }, { "gene_id": 234730, "description": "fucose kinase", "gene_symbol": "[\"Fcsk\"]", "do": null }, { "gene_id": 234734, "description": "alanyl-tRNA synthetase 1", "gene_symbol": "[\"Aars1\"]", "do": null }, { "gene_id": 234736, "description": "ring finger and WD repeat domain 3", "gene_symbol": "[\"Rfwd3\"]", "do": null }, { "gene_id": 234740, "description": "transmembrane protein 231", "gene_symbol": "[\"Tmem231\"]", "do": null }, { "gene_id": 234839, "description": "piezo-type mechanosensitive ion channel component 1", "gene_symbol": "[\"Piezo1\"]", "do": null }, { "gene_id": 234865, "description": "nucleoporin 133", "gene_symbol": "[\"Nup133\"]", "do": null }, { "gene_id": 234889, "description": "guanylate cyclase 1, soluble, alpha 2", "gene_symbol": "[\"Gucy1a2\"]", "do": null }, { "gene_id": 234967, "description": "solute carrier family 36 (proton/amino acid symporter), member 4", "gene_symbol": "[\"Slc36a4\"]", "do": null }, { "gene_id": 235041, "description": "KN motif and ankyrin repeat domains 2", "gene_symbol": "[\"Kank2\"]", "do": null }, { "gene_id": 235044, "description": "phospholipid phosphatase related 2", "gene_symbol": "[\"Plppr2\"]", "do": null }, { "gene_id": 235106, "description": "neurotrimin", "gene_symbol": "[\"Ntm\"]", "do": null }, { "gene_id": 235130, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 15", "gene_symbol": "[\"Adamts15\"]", "do": null }, { "gene_id": 235134, "description": "nuclear factor related to kappa B binding protein", "gene_symbol": "[\"Nfrkb\"]", "do": null }, { "gene_id": 235281, "description": "sodium channel, voltage-gated, type III, beta", "gene_symbol": "[\"Scn3b\"]", "do": "[{\"label\":\"Brugada syndrome 7\",\"id\":\"DOID:0110224\"}]" }, { "gene_id": 235312, "description": "C1q and tumor necrosis factor related protein 5", "gene_symbol": "[\"C1qtnf5\"]", "do": "[{\"label\":\"late-onset retinal degeneration\",\"id\":\"DOID:0060869\"}]" }, { "gene_id": 235315, "description": "ring finger protein 214", "gene_symbol": "[\"Rnf214\"]", "do": null }, { "gene_id": 235339, "description": "dihydrolipoamide S-acetyltransferase", "gene_symbol": "[\"Dlat\"]", "do": null }, { "gene_id": 235344, "description": "salt inducible kinase 2", "gene_symbol": "[\"Sik2\"]", "do": null }, { "gene_id": 235379, "description": "gliomedin", "gene_symbol": "[\"Gldn\"]", "do": null }, { "gene_id": 235380, "description": "Dmx-like 2", "gene_symbol": "[\"Dmxl2\"]", "do": null }, { "gene_id": 235402, "description": "leucine rich repeat and Ig domain containing 1", "gene_symbol": "[\"Lingo1\"]", "do": null }, { "gene_id": 235416, "description": "lectin, mannose-binding 1 like", "gene_symbol": "[\"Lman1l\"]", "do": null }, { "gene_id": 235431, "description": "coronin, actin binding protein, 2B", "gene_symbol": "[\"Coro2b\"]", "do": null }, { "gene_id": 235435, "description": "lactase-like", "gene_symbol": "[\"Lctl\"]", "do": null }, { "gene_id": 235439, "description": "HECT and RLD domain containing E3 ubiquitin protein ligase family member 1", "gene_symbol": "[\"Herc1\"]", "do": null }, { "gene_id": 235442, "description": "RAB8B, member RAS oncogene family", "gene_symbol": "[\"Rab8b\"]", "do": null }, { "gene_id": 235472, "description": "protogenin", "gene_symbol": "[\"Prtg\"]", "do": null }, { "gene_id": 235504, "description": "solute carrier family 17 (anion/sugar transporter), member 5", "gene_symbol": "[\"Slc17a5\"]", "do": "[{\"label\":\"lysosomal storage disease\",\"id\":\"DOID:3211\"},{\"label\":\"sialuria\",\"id\":\"DOID:3659\"}]" }, { "gene_id": 235505, "description": "CD109 antigen", "gene_symbol": "[\"Cd109\"]", "do": null }, { "gene_id": 235533, "description": "glycerol kinase 5", "gene_symbol": "[\"Gk5\"]", "do": null }, { "gene_id": 235534, "description": "2-phosphoxylose phosphatase 1", "gene_symbol": "[\"Pxylp1\"]", "do": null }, { "gene_id": 235582, "description": "glycerate kinase", "gene_symbol": "[\"Glyctk\"]", "do": null }, { "gene_id": 235587, "description": "poly (ADP-ribose) polymerase family, member 3", "gene_symbol": "[\"Parp3\"]", "do": null }, { "gene_id": 235604, "description": "CaM kinase-like vesicle-associated", "gene_symbol": "[\"Camkv\"]", "do": null }, { "gene_id": 235611, "description": "plexin B1", "gene_symbol": "[\"Plxnb1\"]", "do": null }, { "gene_id": 235623, "description": "SREBF chaperone", "gene_symbol": "[\"Scap\"]", "do": null }, { "gene_id": 235626, "description": "SET domain containing 2", "gene_symbol": "[\"Setd2\"]", "do": null }, { "gene_id": 235628, "description": "serine protease 42", "gene_symbol": "[\"Prss42\"]", "do": null }, { "gene_id": 235631, "description": "serine protease 50", "gene_symbol": "[\"Prss50\"]", "do": null }, { "gene_id": 235661, "description": "dynein cytoplasmic 1 light intermediate chain 1", "gene_symbol": "[\"Dync1li1\"]", "do": null }, { "gene_id": 235674, "description": "acetyl-Coenzyme A acyltransferase 1B", "gene_symbol": "[\"Acaa1b\"]", "do": null }, { "gene_id": 235682, "description": "zinc finger protein 445", "gene_symbol": "[\"Zfp445\"]", "do": null }, { "gene_id": 235854, "description": "MAS-related GPR, member A4", "gene_symbol": "[\"Mrgpra4\"]", "do": null }, { "gene_id": 235973, "description": "prostate and testis expressed 14", "gene_symbol": "[\"Pate14\"]", "do": null }, { "gene_id": 236149, "description": "solute carrier family 22 (organic cation transporter), member 26", "gene_symbol": "[\"Slc22a26\"]", "do": null }, { "gene_id": 236266, "description": "ALMS1, centrosome and basal body associated", "gene_symbol": "[\"Alms1\"]", "do": "[{\"label\":\"Alstrom syndrome\",\"id\":\"DOID:0050473\"},{\"label\":\"obesity\",\"id\":\"DOID:9970\"}]" }, { "gene_id": 236285, "description": "LanC lantibiotic synthetase component C-like 3 (bacterial)", "gene_symbol": "[\"Lancl3\"]", "do": null }, { "gene_id": 236293, "description": "solute carrier family 22. member 29", "gene_symbol": "[\"Slc22a29\"]", "do": null }, { "gene_id": 236574, "description": "sperm motility kinase 2B", "gene_symbol": "[\"Smok2b\"]", "do": null }, { "gene_id": 236576, "description": "sprouty RTK signaling antagonist 3", "gene_symbol": "[\"Spry3\"]", "do": null }, { "gene_id": 236690, "description": "nyctalopin", "gene_symbol": "[\"Nyx\"]", "do": "[{\"label\":\"congenital stationary night blindness 1A\",\"id\":\"DOID:0110870\"}]" }, { "gene_id": 236727, "description": "solute carrier family 9 (sodium/hydrogen exchanger), member 7", "gene_symbol": "[\"Slc9a7\"]", "do": null }, { "gene_id": 236732, "description": "RNA binding motif protein 10", "gene_symbol": "[\"Rbm10\"]", "do": null }, { "gene_id": 236794, "description": "solute carrier family 9 (sodium/hydrogen exchanger), member 6", "gene_symbol": "[\"Slc9a6\"]", "do": "[{\"label\":\"Christianson syndrome\",\"id\":\"DOID:0060825\"}]" }, { "gene_id": 237038, "description": "NADPH oxidase 1", "gene_symbol": "[\"Nox1\"]", "do": null }, { "gene_id": 237091, "description": "lipoma HMGIC fusion partner-like 1", "gene_symbol": "[\"Lhfpl1\"]", "do": null }, { "gene_id": 237175, "description": "adhesion G protein-coupled receptor G2", "gene_symbol": "[\"Adgrg2\"]", "do": null }, { "gene_id": 237213, "description": "glycine receptor, alpha 2 subunit", "gene_symbol": "[\"Glra2\"]", "do": null }, { "gene_id": 237222, "description": "OFD1, centriole and centriolar satellite protein", "gene_symbol": "[\"Ofd1\"]", "do": "[{\"label\":\"orofaciodigital syndrome I\",\"id\":\"DOID:0060316\"}]" }, { "gene_id": 237253, "description": "low density lipoprotein receptor-related protein 11", "gene_symbol": "[\"Lrp11\"]", "do": null }, { "gene_id": 237313, "description": "interleukin 20 receptor, alpha", "gene_symbol": "[\"Il20ra\"]", "do": null }, { "gene_id": 237353, "description": "SH3 domain containing ring finger 3", "gene_symbol": "[\"Sh3rf3\"]", "do": null }, { "gene_id": 237397, "description": "C2 calcium-dependent domain containing 4C", "gene_symbol": "[\"C2cd4c\"]", "do": null }, { "gene_id": 237400, "description": "mex3 RNA binding family member D", "gene_symbol": "[\"Mex3d\"]", "do": null }, { "gene_id": 237403, "description": "leucine rich repeat and Ig domain containing 3", "gene_symbol": "[\"Lingo3\"]", "do": null }, { "gene_id": 237500, "description": "transmembrane and tetratricopeptide repeat containing 3", "gene_symbol": "[\"Tmtc3\"]", "do": null }, { "gene_id": 237523, "description": "protein tyrosine phosphatase receptor type Q", "gene_symbol": "[\"Ptprq\"]", "do": null }, { "gene_id": 237553, "description": "TRH-degrading enzyme", "gene_symbol": "[\"Trhde\"]", "do": null }, { "gene_id": 237625, "description": "phospholipase A2, group III", "gene_symbol": "[\"Pla2g3\"]", "do": null }, { "gene_id": 237716, "description": "G protein-coupled receptor 75", "gene_symbol": "[\"Gpr75\"]", "do": null }, { "gene_id": 237754, "description": "butyrophilin-like 9", "gene_symbol": "[\"Btnl9\"]", "do": null }, { "gene_id": 237823, "description": "phosphoribosylformylglycinamidine synthase (FGAR amidotransferase)", "gene_symbol": "[\"Pfas\"]", "do": null }, { "gene_id": 237831, "description": "solute carrier family 13 (sodium-dependent citrate transporter), member 5", "gene_symbol": "[\"Slc13a5\"]", "do": null }, { "gene_id": 237847, "description": "reticulon 4 receptor-like 1", "gene_symbol": "[\"Rtn4rl1\"]", "do": null }, { "gene_id": 237868, "description": "sterile alpha and HEAT/Armadillo motif containing 1", "gene_symbol": "[\"Sarm1\"]", "do": null }, { "gene_id": 237877, "description": "ATPase family, AAA domain containing 5", "gene_symbol": "[\"Atad5\"]", "do": null }, { "gene_id": 237940, "description": "amine oxidase copper containing 2", "gene_symbol": "[\"Aoc2\"]", "do": null }, { "gene_id": 237943, "description": "G patch domain containing 8", "gene_symbol": "[\"Gpatch8\"]", "do": null }, { "gene_id": 237958, "description": "signal peptide peptidase 2C", "gene_symbol": "[\"Sppl2c\"]", "do": null }, { "gene_id": 237979, "description": "sidekick cell adhesion molecule 2", "gene_symbol": "[\"Sdk2\"]", "do": null }, { "gene_id": 238011, "description": "ectonucleotide pyrophosphatase/phosphodiesterase 7", "gene_symbol": "[\"Enpp7\"]", "do": null }, { "gene_id": 238023, "description": "hexosaminidase D", "gene_symbol": "[\"Hexd\"]", "do": null }, { "gene_id": 238055, "description": "apolipoprotein B", "gene_symbol": "[\"Apob\"]", "do": "[{\"label\":\"familial hypobetalipoproteinemia 2\",\"id\":\"DOID:0111061\"}]" }, { "gene_id": 238057, "description": "growth differentiation factor 7", "gene_symbol": "[\"Gdf7\"]", "do": null }, { "gene_id": 238130, "description": "dedicator of cytokinesis 4", "gene_symbol": "[\"Dock4\"]", "do": null }, { "gene_id": 238205, "description": "leucine rich repeat and fibronectin type III domain containing 5", "gene_symbol": "[\"Lrfn5\"]", "do": null }, { "gene_id": 238252, "description": "G protein-coupled receptor 135", "gene_symbol": "[\"Gpr135\"]", "do": null }, { "gene_id": 238257, "description": "cell division cycle 50 P4-ATPase accessory subunit B", "gene_symbol": "[\"Cdc50b\"]", "do": null }, { "gene_id": 238271, "description": "potassium voltage-gated channel, subfamily H (eag-related), member 5", "gene_symbol": "[\"Kcnh5\"]", "do": null }, { "gene_id": 238276, "description": "A kinase anchor protein 5", "gene_symbol": "[\"Akap5\"]", "do": null }, { "gene_id": 238330, "description": "interferon regulatory factor 2 binding protein-like", "gene_symbol": "[\"Irf2bpl\"]", "do": null }, { "gene_id": 238377, "description": "G protein-coupled receptor 68", "gene_symbol": "[\"Gpr68\"]", "do": null }, { "gene_id": 238384, "description": "solute carrier family 24 (sodium/potassium/calcium exchanger), member 4", "gene_symbol": "[\"Slc24a4\"]", "do": null }, { "gene_id": 238393, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 3F", "gene_symbol": "[\"Serpina3f\"]", "do": null }, { "gene_id": 238395, "description": "serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 3J", "gene_symbol": "[\"Serpina3j\"]", "do": null }, { "gene_id": 238405, "description": "a disintegrin and metallopeptidase domain 6B", "gene_symbol": "[\"Adam6b\"]", "do": null }, { "gene_id": 238406, "description": "a disintegrin and metallopeptidase domain 6A", "gene_symbol": "[\"Adam6a\"]", "do": null }, { "gene_id": 238555, "description": "butyrophilin, subfamily 2, member A2", "gene_symbol": "[\"Btn2a2\"]", "do": null }, { "gene_id": 238663, "description": "spermatogenesis associated 31 subfamily D, member 1D", "gene_symbol": "[\"Spata31d1d\"]", "do": null }, { "gene_id": 238880, "description": "actin, beta-like 2", "gene_symbol": "[\"Actbl2\"]", "do": null }, { "gene_id": 238988, "description": "ELKS/RAB6-interacting/CAST family member 2", "gene_symbol": "[\"Erc2\"]", "do": null }, { "gene_id": 239029, "description": "anthrax toxin receptor-like", "gene_symbol": "[\"Antxrl\"]", "do": null }, { "gene_id": 239037, "description": "leucine-rich repeat, immunoglobulin-like and transmembrane domains 1", "gene_symbol": "[\"Lrit1\"]", "do": null }, { "gene_id": 239038, "description": "leucine-rich repeat, immunoglobulin-like and transmembrane domains 2", "gene_symbol": "[\"Lrit2\"]", "do": null }, { "gene_id": 239081, "description": "toll-like receptor 11", "gene_symbol": "[\"Tlr11\"]", "do": null }, { "gene_id": 239096, "description": "cadherin-like 24", "gene_symbol": "[\"Cdh24\"]", "do": null }, { "gene_id": 239102, "description": "zinc finger homeobox 2", "gene_symbol": "[\"Zfhx2\"]", "do": "[{\"label\":\"Marsili syndrome\",\"id\":\"DOID:0081075\"}]" }, { "gene_id": 239126, "description": "C1q and tumor necrosis factor related protein 9", "gene_symbol": "[\"C1qtnf9\"]", "do": null }, { "gene_id": 239167, "description": "syncytin b", "gene_symbol": "[\"Synb\"]", "do": null }, { "gene_id": 239217, "description": "potassium channel tetramerisation domain containing 12", "gene_symbol": "[\"Kctd12\"]", "do": null }, { "gene_id": 239283, "description": "oxoglutarate (alpha-ketoglutarate) receptor 1", "gene_symbol": "[\"Oxgr1\"]", "do": null }, { "gene_id": 239336, "description": "relaxin family peptide receptor 3", "gene_symbol": "[\"Rxfp3\"]", "do": null }, { "gene_id": 239337, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 12", "gene_symbol": "[\"Adamts12\"]", "do": null }, { "gene_id": 239393, "description": "low density lipoprotein-related protein 12", "gene_symbol": "[\"Lrp12\"]", "do": null }, { "gene_id": 239405, "description": "R-spondin 2", "gene_symbol": "[\"Rspo2\"]", "do": null }, { "gene_id": 239420, "description": "CUB and Sushi multiple domains 3", "gene_symbol": "[\"Csmd3\"]", "do": null }, { "gene_id": 239447, "description": "collectin sub-family member 10", "gene_symbol": "[\"Colec10\"]", "do": null }, { "gene_id": 239528, "description": "argonaute RISC catalytic subunit 2", "gene_symbol": "[\"Ago2\"]", "do": null }, { "gene_id": 239530, "description": "G protein-coupled receptor 20", "gene_symbol": "[\"Gpr20\"]", "do": null }, { "gene_id": 239554, "description": "FAD-dependent oxidoreductase domain containing 2", "gene_symbol": "[\"Foxred2\"]", "do": null }, { "gene_id": 239559, "description": "alpha 1,4-galactosyltransferase", "gene_symbol": "[\"A4galt\"]", "do": null }, { "gene_id": 239606, "description": "solute carrier family 2 (facilitated glucose transporter), member 13", "gene_symbol": "[\"Slc2a13\"]", "do": null }, { "gene_id": 239611, "description": "mucin 19", "gene_symbol": "[\"Muc19\"]", "do": "[{\"label\":\"Sjogren's syndrome\",\"id\":\"DOID:12894\"}]" }, { "gene_id": 239667, "description": "disco interacting protein 2 homolog B", "gene_symbol": "[\"Dip2b\"]", "do": null }, { "gene_id": 239719, "description": "myocardin related transcription factor B", "gene_symbol": "[\"Mrtfb\"]", "do": null }, { "gene_id": 239731, "description": "RIMS binding protein 3", "gene_symbol": "[\"Rimbp3\"]", "do": null }, { "gene_id": 239739, "description": "lysosomal-associated membrane protein 3", "gene_symbol": "[\"Lamp3\"]", "do": null }, { "gene_id": 239759, "description": "lipase H", "gene_symbol": "[\"Liph\"]", "do": null }, { "gene_id": 239827, "description": "phosphatidylinositol glycan anchor biosynthesis, class Z", "gene_symbol": "[\"Pigz\"]", "do": null }, { "gene_id": 239839, "description": "coiled-coil domain containing 14", "gene_symbol": "[\"Ccdc14\"]", "do": null }, { "gene_id": 239845, "description": "G protein-coupled receptor 156", "gene_symbol": "[\"Gpr156\"]", "do": null }, { "gene_id": 239849, "description": "CD200 receptor 4", "gene_symbol": "[\"Cd200r4\"]", "do": null }, { "gene_id": 239852, "description": "zona pellucida like domain containing 1", "gene_symbol": "[\"Zpld1\"]", "do": null }, { "gene_id": 239853, "description": "adhesion G protein-coupled receptor G7", "gene_symbol": "[\"Adgrg7\"]", "do": null }, { "gene_id": 239857, "description": "cell adhesion molecule 2", "gene_symbol": "[\"Cadm2\"]", "do": null }, { "gene_id": 239985, "description": "AT-rich interaction domain 1B", "gene_symbol": "[\"Arid1b\"]", "do": null }, { "gene_id": 240028, "description": "leucyl/cystinyl aminopeptidase", "gene_symbol": "[\"Lnpep\"]", "do": null }, { "gene_id": 240057, "description": "synaptic Ras GTPase activating protein 1 homolog (rat)", "gene_symbol": "[\"Syngap1\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 240069, "description": "microrchidia 2B", "gene_symbol": "[\"Morc2b\"]", "do": null }, { "gene_id": 240087, "description": "mediator of DNA damage checkpoint 1", "gene_symbol": "[\"Mdc1\"]", "do": null }, { "gene_id": 240119, "description": "beta galactoside alpha 2,6 sialyltransferase 2", "gene_symbol": "[\"St6gal2\"]", "do": null }, { "gene_id": 240185, "description": "junctional cadherin 5 associated", "gene_symbol": "[\"Jcad\"]", "do": null }, { "gene_id": 240215, "description": "solute carrier family 4, sodium bicarbonate cotransporter, member 9", "gene_symbol": "[\"Slc4a9\"]", "do": null }, { "gene_id": 240239, "description": "G protein-coupled receptor 151", "gene_symbol": "[\"Gpr151\"]", "do": null }, { "gene_id": 240322, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 19", "gene_symbol": "[\"Adamts19\"]", "do": "[{\"label\":\"aortic valve disease\",\"id\":\"DOID:62\"}]" }, { "gene_id": 240332, "description": "solute carrier family 6 (neurotransmitter transporter, L-proline), member 7", "gene_symbol": "[\"Slc6a7\"]", "do": null }, { "gene_id": 240334, "description": "prenylcysteine oxidase 1 like", "gene_symbol": "[\"Pcyox1l\"]", "do": null }, { "gene_id": 240411, "description": "lipoxygenase homology domains 1", "gene_symbol": "[\"Loxhd1\"]", "do": null }, { "gene_id": 240427, "description": "SET binding protein 1", "gene_symbol": "[\"Setbp1\"]", "do": null }, { "gene_id": 240442, "description": "ADNP homeobox 2", "gene_symbol": "[\"Adnp2\"]", "do": null }, { "gene_id": 240595, "description": "potassium channel, subfamily V, member 2", "gene_symbol": "[\"Kcnv2\"]", "do": null }, { "gene_id": 240613, "description": "bromodomain containing 10", "gene_symbol": "[\"Brd10\"]", "do": null }, { "gene_id": 240633, "description": "lipase family member K", "gene_symbol": "[\"Lipk\"]", "do": null }, { "gene_id": 240667, "description": "SEC31 homolog B, COPII coat complex component", "gene_symbol": "[\"Sec31b\"]", "do": null }, { "gene_id": 240675, "description": "von Willebrand factor A domain containing 2", "gene_symbol": "[\"Vwa2\"]", "do": null }, { "gene_id": 240690, "description": "suppression of tumorigenicity 18", "gene_symbol": "[\"St18\"]", "do": null }, { "gene_id": 240725, "description": "sulfatase 1", "gene_symbol": "[\"Sulf1\"]", "do": null }, { "gene_id": 240819, "description": "transmembrane epididymal protein 1A", "gene_symbol": "[\"Teddm1a\"]", "do": null }, { "gene_id": 240832, "description": "torsin A interacting protein 2", "gene_symbol": "[\"Tor1aip2\"]", "do": null }, { "gene_id": 240843, "description": "bone morphogenic protein/retinoic acid inducible neural-specific 2", "gene_symbol": "[\"Brinp2\"]", "do": null }, { "gene_id": 240873, "description": "tumor necrosis factor (ligand) superfamily, member 18", "gene_symbol": "[\"Tnfsf18\"]", "do": null }, { "gene_id": 240888, "description": "G protein-coupled receptor 161", "gene_symbol": "[\"Gpr161\"]", "do": null }, { "gene_id": 240899, "description": "leucine rich repeat containing 52", "gene_symbol": "[\"Lrrc52\"]", "do": null }, { "gene_id": 240913, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 4", "gene_symbol": "[\"Adamts4\"]", "do": null }, { "gene_id": 241035, "description": "polycystic kidney and hepatic disease 1", "gene_symbol": "[\"Pkhd1\"]", "do": "[{\"label\":\"Caroli syndrome\",\"id\":\"DOID:0081394\"},{\"label\":\"autosomal recessive polycystic kidney disease\",\"id\":\"DOID:0110861\"},{\"label\":\"polycystic kidney disease 4\",\"id\":\"DOID:0080212\"}]" }, { "gene_id": 241062, "description": "post-GPI attachment to proteins 1", "gene_symbol": "[\"Pgap1\"]", "do": "[{\"label\":\"holoprosencephaly\",\"id\":\"DOID:4621\"}]" }, { "gene_id": 241070, "description": "chemerin chemokine-like receptor 2", "gene_symbol": "[\"Cmklr2\"]", "do": null }, { "gene_id": 241073, "description": "dystrotelin", "gene_symbol": "[\"Dytn\"]", "do": null }, { "gene_id": 241118, "description": "acid-sensing ion channel family member 4", "gene_symbol": "[\"Asic4\"]", "do": null }, { "gene_id": 241159, "description": "sialidase 4", "gene_symbol": "[\"Neu4\"]", "do": null }, { "gene_id": 241175, "description": "contactin associated protein-like 5B", "gene_symbol": "[\"Cntnap5b\"]", "do": null }, { "gene_id": 241201, "description": "cadherin 7, type 2", "gene_symbol": "[\"Cdh7\"]", "do": null }, { "gene_id": 241226, "description": "integrin alpha 8", "gene_symbol": "[\"Itga8\"]", "do": null }, { "gene_id": 241230, "description": "ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6", "gene_symbol": "[\"St8sia6\"]", "do": null }, { "gene_id": 241263, "description": "G protein-coupled receptor 158", "gene_symbol": "[\"Gpr158\"]", "do": null }, { "gene_id": 241296, "description": "leucine rich repeat containing 8A VRAC subunit A", "gene_symbol": "[\"Lrrc8a\"]", "do": null }, { "gene_id": 241324, "description": "crumbs family member 2", "gene_symbol": "[\"Crb2\"]", "do": "[{\"label\":\"retinitis pigmentosa\",\"id\":\"DOID:10584\"}]" }, { "gene_id": 241391, "description": "polypeptide N-acetylgalactosaminyltransferase 5", "gene_symbol": "[\"Galnt5\"]", "do": null }, { "gene_id": 241431, "description": "xin actin-binding repeat containing 2", "gene_symbol": "[\"Xirp2\"]", "do": null }, { "gene_id": 241447, "description": "ceramide synthase 6", "gene_symbol": "[\"Cers6\"]", "do": null }, { "gene_id": 241494, "description": "zinc finger protein 385B", "gene_symbol": "[\"Zfp385b\"]", "do": null }, { "gene_id": 241520, "description": "family with sequence similarity 171, member B", "gene_symbol": "[\"Fam171b\"]", "do": null }, { "gene_id": 241528, "description": "leucine rich repeat containing 55", "gene_symbol": "[\"Lrrc55\"]", "do": null }, { "gene_id": 241556, "description": "tetraspanin 18", "gene_symbol": "[\"Tspan18\"]", "do": null }, { "gene_id": 241568, "description": "leucine rich repeat containing 4C", "gene_symbol": "[\"Lrrc4c\"]", "do": null }, { "gene_id": 241576, "description": "low density lipoprotein receptor class A domain containing 3", "gene_symbol": "[\"Ldlrad3\"]", "do": null }, { "gene_id": 241589, "description": "RIKEN cDNA D430041D05 gene", "gene_symbol": "[\"D430041D05Rik\"]", "do": null }, { "gene_id": 241612, "description": "solute carrier family 5 (sodium/glucose cotransporter), member 12", "gene_symbol": "[\"Slc5a12\"]", "do": null }, { "gene_id": 241638, "description": "leucine zipper, putative tumor suppressor family member 3", "gene_symbol": "[\"Lzts3\"]", "do": null }, { "gene_id": 241656, "description": "p21 (RAC1) activated kinase 5", "gene_symbol": "[\"Pak5\"]", "do": null }, { "gene_id": 241727, "description": "syntaphilin", "gene_symbol": "[\"Snph\"]", "do": null }, { "gene_id": 241846, "description": "LSM family member 14B", "gene_symbol": "[\"Lsm14b\"]", "do": null }, { "gene_id": 241877, "description": "solute carrier family 10 (sodium/bile acid cotransporter family), member 5", "gene_symbol": "[\"Slc10a5\"]", "do": null }, { "gene_id": 241915, "description": "polyhomeotic 3", "gene_symbol": "[\"Phc3\"]", "do": null }, { "gene_id": 241919, "description": "solute carrier family 7 (cationic amino acid transporter, y+ system), member 14", "gene_symbol": "[\"Slc7a14\"]", "do": "[{\"label\":\"blindness\",\"id\":\"DOID:1432\"},{\"label\":\"sensorineural hearing loss\",\"id\":\"DOID:10003\"}]" }, { "gene_id": 242022, "description": "Fras1 related extracellular matrix protein 2", "gene_symbol": "[\"Frem2\"]", "do": "[{\"label\":\"Fraser syndrome\",\"id\":\"DOID:0090001\"},{\"label\":\"isolated cryptophthalmia\",\"id\":\"DOID:0111717\"}]" }, { "gene_id": 242050, "description": "immunoglobulin superfamily, member 10", "gene_symbol": "[\"Igsf10\"]", "do": null }, { "gene_id": 242083, "description": "protein phosphatase 1 (formerly 2C)-like", "gene_symbol": "[\"Ppm1l\"]", "do": null }, { "gene_id": 242093, "description": "relaxin family peptide receptor 4", "gene_symbol": "[\"Rxfp4\"]", "do": null }, { "gene_id": 242100, "description": "peptidoglycan recognition protein 3", "gene_symbol": "[\"Pglyrp3\"]", "do": null }, { "gene_id": 242122, "description": "V-set domain containing T cell activation inhibitor 1", "gene_symbol": "[\"Vtcn1\"]", "do": null }, { "gene_id": 242126, "description": "solute carrier family 22 (organic anion/cation transporter), member 15", "gene_symbol": "[\"Slc22a15\"]", "do": null }, { "gene_id": 242235, "description": "leucine-rich repeat, immunoglobulin-like and transmembrane domains 3", "gene_symbol": "[\"Lrit3\"]", "do": "[{\"label\":\"congenital stationary night blindness 1F\",\"id\":\"DOID:0110864\"}]" }, { "gene_id": 242259, "description": "solute carrier family 44, member 5", "gene_symbol": "[\"Slc44a5\"]", "do": null }, { "gene_id": 242274, "description": "leucine rich repeat containing 7", "gene_symbol": "[\"Lrrc7\"]", "do": null }, { "gene_id": 242291, "description": "3'(2'), 5'-bisphosphate nucleotidase 2", "gene_symbol": "[\"Bpnt2\"]", "do": "[{\"label\":\"chondrodysplasia with joint dislocations gPAPP type\",\"id\":\"DOID:0112224\"}]" }, { "gene_id": 242316, "description": "growth differentiation factor 6", "gene_symbol": "[\"Gdf6\"]", "do": null }, { "gene_id": 242362, "description": "mannosidase, endo-alpha", "gene_symbol": "[\"Manea\"]", "do": null }, { "gene_id": 242384, "description": "leucine rich repeat and Ig domain containing 2", "gene_symbol": "[\"Lingo2\"]", "do": null }, { "gene_id": 242409, "description": "transmembrane protein 8B", "gene_symbol": "[\"Tmem8b\"]", "do": null }, { "gene_id": 242418, "description": "DDB1 and CUL4 associated factor 10", "gene_symbol": "[\"Dcaf10\"]", "do": null }, { "gene_id": 242425, "description": "gamma-aminobutyric acid type B receptor subunit 2", "gene_symbol": "[\"Gabbr2\"]", "do": null }, { "gene_id": 242443, "description": "glutamate receptor ionotropic, NMDA3A", "gene_symbol": "[\"Grin3a\"]", "do": null }, { "gene_id": 242466, "description": "zinc finger protein 462", "gene_symbol": "[\"Zfp462\"]", "do": "[{\"label\":\"generalized anxiety disorder\",\"id\":\"DOID:14320\"}]" }, { "gene_id": 242474, "description": "transmembrane protein 245", "gene_symbol": "[\"Tmem245\"]", "do": null }, { "gene_id": 242509, "description": "basonuclin zinc finger protein 2", "gene_symbol": "[\"Bnc2\"]", "do": null }, { "gene_id": 242519, "description": "interferon alpha 12", "gene_symbol": "[\"Ifna12\"]", "do": null }, { "gene_id": 242603, "description": "CUB domain containing protein 2", "gene_symbol": "[\"Cdcp2\"]", "do": null }, { "gene_id": 242607, "description": "solute carrier family 1 (glutamate transporter), member 7", "gene_symbol": "[\"Slc1a7\"]", "do": null }, { "gene_id": 242608, "description": "podocan", "gene_symbol": "[\"Podn\"]", "do": null }, { "gene_id": 242627, "description": "selection and upkeep of intraepithelial T cells 5", "gene_symbol": "[\"Skint5\"]", "do": null }, { "gene_id": 242667, "description": "DLG associated protein 3", "gene_symbol": "[\"Dlgap3\"]", "do": null }, { "gene_id": 242687, "description": "WASP family, member 2", "gene_symbol": "[\"Wasf2\"]", "do": null }, { "gene_id": 242700, "description": "interferon lambda receptor 1", "gene_symbol": "[\"Ifnlr1\"]", "do": null }, { "gene_id": 242702, "description": "myomesin family, member 3", "gene_symbol": "[\"Myom3\"]", "do": null }, { "gene_id": 242721, "description": "kelch domain containing 7A", "gene_symbol": "[\"Klhdc7a\"]", "do": null }, { "gene_id": 242735, "description": "leucine rich repeat containing 38", "gene_symbol": "[\"Lrrc38\"]", "do": null }, { "gene_id": 242939, "description": "carboxypeptidase Z", "gene_symbol": "[\"Cpz\"]", "do": null }, { "gene_id": 243084, "description": "transmembrane protease, serine 11e", "gene_symbol": "[\"Tmprss11e\"]", "do": null }, { "gene_id": 243085, "description": "UDP glucuronosyltransferase 2 family, polypeptide B35", "gene_symbol": "[\"Ugt2b35\"]", "do": null }, { "gene_id": 243168, "description": "hydroxysteroid (17-beta) dehydrogenase 13", "gene_symbol": "[\"Hsd17b13\"]", "do": null }, { "gene_id": 243219, "description": "RIKEN cDNA 2900026A02 gene", "gene_symbol": "[\"2900026A02Rik\"]", "do": null }, { "gene_id": 243270, "description": "hydrocarboxylic acid receptor 1", "gene_symbol": "[\"Hcar1\"]", "do": null }, { "gene_id": 243277, "description": "adhesion G protein-coupled receptor D1", "gene_symbol": "[\"Adgrd1\"]", "do": null }, { "gene_id": 243300, "description": "neuronal tyrosine-phosphorylated phosphoinositide 3-kinase adaptor 1", "gene_symbol": "[\"Nyap1\"]", "do": null }, { "gene_id": 243312, "description": "leucine rich repeat and fibronectin type III, extracellular 1", "gene_symbol": "[\"Elfn1\"]", "do": null }, { "gene_id": 243328, "description": "solute carrier family 29 (nucleoside transporters), member 4", "gene_symbol": "[\"Slc29a4\"]", "do": null }, { "gene_id": 243339, "description": "transmembrane protein 130", "gene_symbol": "[\"Tmem130\"]", "do": null }, { "gene_id": 243385, "description": "GPRIN family member 3", "gene_symbol": "[\"Gprin3\"]", "do": null }, { "gene_id": 243499, "description": "leucine rich repeat transmembrane neuronal 4", "gene_symbol": "[\"Lrrtm4\"]", "do": null }, { "gene_id": 243548, "description": "prickle planar cell polarity protein 2", "gene_symbol": "[\"Prickle2\"]", "do": null }, { "gene_id": 243616, "description": "solute carrier family 6 (neurotransmitter transporter, GABA), member 11", "gene_symbol": "[\"Slc6a11\"]", "do": null }, { "gene_id": 243634, "description": "anoctamin 2", "gene_symbol": "[\"Ano2\"]", "do": null }, { "gene_id": 243653, "description": "C-type lectin domain family 1, member a", "gene_symbol": "[\"Clec1a\"]", "do": null }, { "gene_id": 243655, "description": "killer cell lectin-like receptor family E member 1", "gene_symbol": "[\"Klre1\"]", "do": null }, { "gene_id": 243743, "description": "plexin A4", "gene_symbol": "[\"Plxna4\"]", "do": null }, { "gene_id": 243764, "description": "cholinergic receptor, muscarinic 2, cardiac", "gene_symbol": "[\"Chrm2\"]", "do": null }, { "gene_id": 243771, "description": "poly (ADP-ribose) polymerase family, member 12", "gene_symbol": "[\"Parp12\"]", "do": null }, { "gene_id": 243780, "description": "DENN domain containing 11", "gene_symbol": "[\"Dennd11\"]", "do": null }, { "gene_id": 243816, "description": "glycoprotein 6 platelet", "gene_symbol": "[\"Gp6\"]", "do": null }, { "gene_id": 243819, "description": "protein phosphatase 6, regulatory subunit 1", "gene_symbol": "[\"Ppp6r1\"]", "do": null }, { "gene_id": 243842, "description": "BRD4 interacting chromatin remodeling complex associated protein", "gene_symbol": "[\"Bicra\"]", "do": null }, { "gene_id": 243853, "description": "fukutin related protein", "gene_symbol": "[\"Fkrp\"]", "do": "[{\"label\":\"autosomal recessive limb-girdle muscular dystrophy type 2I\",\"id\":\"DOID:0110299\"},{\"label\":\"muscular dystrophy-dystroglycanopathy type B1\",\"id\":\"DOID:0050588\"},{\"label\":\"muscular dystrophy-dystroglycanopathy type B5\",\"id\":\"DOID:0110635\"},{\"label\":\"muscular dystrophy\",\"id\":\"DOID:9884\"}]" }, { "gene_id": 243862, "description": "pregnancy-specific beta-1-glycoprotein 22", "gene_symbol": "[\"Psg22\"]", "do": null }, { "gene_id": 243864, "description": "MHC I like leukocyte 2", "gene_symbol": "[\"Mill2\"]", "do": null }, { "gene_id": 243911, "description": "kirre like nephrin family adhesion molecule 2", "gene_symbol": "[\"Kirrel2\"]", "do": null }, { "gene_id": 243912, "description": "heat shock protein family B (small) member 6", "gene_symbol": "[\"Hspb6\"]", "do": null }, { "gene_id": 243914, "description": "leucine-rich repeat LGI family, member 4", "gene_symbol": "[\"Lgi4\"]", "do": null }, { "gene_id": 243958, "description": "sialic acid binding Ig-like lectin G", "gene_symbol": "[\"Siglecg\"]", "do": null }, { "gene_id": 243961, "description": "SH3 and multiple ankyrin repeat domains 1", "gene_symbol": "[\"Shank1\"]", "do": null }, { "gene_id": 243967, "description": "netrin 5", "gene_symbol": "[\"Ntn5\"]", "do": null }, { "gene_id": 243978, "description": "MAS-related GPR, member X2", "gene_symbol": "[\"Mrgprx2\"]", "do": null }, { "gene_id": 243979, "description": "MAS-related GPR, member B2", "gene_symbol": "[\"Mrgprb2\"]", "do": null }, { "gene_id": 243996, "description": "RIKEN cDNA 4933405O20 gene", "gene_symbol": "[\"4933405O20Rik\"]", "do": null }, { "gene_id": 244058, "description": "repulsive guidance molecule family member A", "gene_symbol": "[\"Rgma\"]", "do": null }, { "gene_id": 244152, "description": "tsukushi, small leucine rich proteoglycan", "gene_symbol": "[\"Tsku\"]", "do": null }, { "gene_id": 244198, "description": "olfactomedin-like 1", "gene_symbol": "[\"Olfml1\"]", "do": null }, { "gene_id": 244199, "description": "ovochymase 2", "gene_symbol": "[\"Ovch2\"]", "do": null }, { "gene_id": 244216, "description": "zinc finger protein 771", "gene_symbol": "[\"Zfp771\"]", "do": null }, { "gene_id": 244218, "description": "cardiotrophin 2", "gene_symbol": "[\"Ctf2\"]", "do": null }, { "gene_id": 244237, "description": "tumor necrosis factor receptor superfamily, member 26", "gene_symbol": "[\"Tnfrsf26\"]", "do": null }, { "gene_id": 244238, "description": "MAS-related GPR, member E", "gene_symbol": "[\"Mrgpre\"]", "do": null }, { "gene_id": 244310, "description": "DLG associated protein 2", "gene_symbol": "[\"Dlgap2\"]", "do": null }, { "gene_id": 244373, "description": "ER lipid raft associated 2", "gene_symbol": "[\"Erlin2\"]", "do": null }, { "gene_id": 244416, "description": "protein phosphatase 1, regulatory subunit 3B", "gene_symbol": "[\"Ppp1r3b\"]", "do": null }, { "gene_id": 244418, "description": "PEAK1 related kinase activating pseudokinase 1", "gene_symbol": "[\"Prag1\"]", "do": null }, { "gene_id": 244431, "description": "sarcoglycan zeta", "gene_symbol": "[\"Sgcz\"]", "do": null }, { "gene_id": 244550, "description": "podocan-like 1", "gene_symbol": "[\"Podnl1\"]", "do": null }, { "gene_id": 244562, "description": "ATP-binding cassette, sub-family C member 12", "gene_symbol": "[\"Abcc12\"]", "do": null }, { "gene_id": 244646, "description": "polycystic kidney disease 1 like 3", "gene_symbol": "[\"Pkd1l3\"]", "do": null }, { "gene_id": 244653, "description": "HYDIN, axonemal central pair apparatus protein", "gene_symbol": "[\"Hydin\"]", "do": null }, { "gene_id": 244654, "description": "MTSS I-BAR domain containing 2", "gene_symbol": "[\"Mtss2\"]", "do": null }, { "gene_id": 244668, "description": "signal-induced proliferation-associated 1 like 2", "gene_symbol": "[\"Sipa1l2\"]", "do": null }, { "gene_id": 244682, "description": "contactin 5", "gene_symbol": "[\"Cntn5\"]", "do": null }, { "gene_id": 244694, "description": "lysine (K)-specific demethylase 4D", "gene_symbol": "[\"Kdm4d\"]", "do": null }, { "gene_id": 244698, "description": "hephaestin-like 1", "gene_symbol": "[\"Hephl1\"]", "do": null }, { "gene_id": 244723, "description": "olfactomedin 2", "gene_symbol": "[\"Olfm2\"]", "do": null }, { "gene_id": 244745, "description": "dpy-19 like C-mannosyltransferase 1", "gene_symbol": "[\"Dpy19l1\"]", "do": null }, { "gene_id": 244757, "description": "galactosidase, beta 1-like 2", "gene_symbol": "[\"Glb1l2\"]", "do": null }, { "gene_id": 244853, "description": "neurexophilin and PC-esterase domain family, member 4", "gene_symbol": "[\"Nxpe4\"]", "do": null }, { "gene_id": 244859, "description": "ankyrin repeat and kinase domain containing 1", "gene_symbol": "[\"Ankk1\"]", "do": null }, { "gene_id": 244864, "description": "layilin", "gene_symbol": "[\"Layn\"]", "do": null }, { "gene_id": 244867, "description": "Rho GTPase activating protein 20", "gene_symbol": "[\"Arhgap20\"]", "do": null }, { "gene_id": 244886, "description": "transmembrane protein 266", "gene_symbol": "[\"Tmem266\"]", "do": null }, { "gene_id": 244895, "description": "pseudopodium-enriched atypical kinase 1", "gene_symbol": "[\"Peak1\"]", "do": null }, { "gene_id": 244954, "description": "serine protease 35", "gene_symbol": "[\"Prss35\"]", "do": null }, { "gene_id": 244958, "description": "melanocortin 2 receptor accessory protein 2", "gene_symbol": "[\"Mrap2\"]", "do": null }, { "gene_id": 245026, "description": "collagen, type VI, alpha 6", "gene_symbol": "[\"Col6a6\"]", "do": null }, { "gene_id": 245050, "description": "golgi associated kinase 1A", "gene_symbol": "[\"Gask1a\"]", "do": null }, { "gene_id": 245126, "description": "T cell-interacting, activating receptor on myeloid cells 1", "gene_symbol": "[\"Tarm1\"]", "do": null }, { "gene_id": 245269, "description": "NIM1 serine/threonine protein kinase", "gene_symbol": "[\"Nim1k\"]", "do": null }, { "gene_id": 245424, "description": "G protein-coupled receptor 101", "gene_symbol": "[\"Gpr101\"]", "do": null }, { "gene_id": 245446, "description": "SLIT and NTRK-like family, member 4", "gene_symbol": "[\"Slitrk4\"]", "do": null }, { "gene_id": 245450, "description": "SLIT and NTRK-like family, member 2", "gene_symbol": "[\"Slitrk2\"]", "do": "[{\"label\":\"non-syndromic X-linked intellectual developmental disorder 111\",\"id\":\"DOID:0060929\"}]" }, { "gene_id": 245474, "description": "dyskeratosis congenita 1, dyskerin", "gene_symbol": "[\"Dkc1\"]", "do": "[{\"label\":\"dyskeratosis congenita\",\"id\":\"DOID:2729\"}]" }, { "gene_id": 245527, "description": "ectodysplasin A2 receptor", "gene_symbol": "[\"Eda2r\"]", "do": null }, { "gene_id": 245537, "description": "neuroligin 3", "gene_symbol": "[\"Nlgn3\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 245555, "description": "neurite extension and migration factor", "gene_symbol": "[\"Nexmif\"]", "do": null }, { "gene_id": 245607, "description": "G protein-coupled receptor associated sorting protein 2", "gene_symbol": "[\"Gprasp2\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"},{\"label\":\"intellectual disability\",\"id\":\"DOID:1059\"}]" }, { "gene_id": 245643, "description": "FERM and PDZ domain containing 3", "gene_symbol": "[\"Frmpd3\"]", "do": null }, { "gene_id": 245666, "description": "IQ motif and Sec7 domain 2", "gene_symbol": "[\"Iqsec2\"]", "do": "[{\"label\":\"non-syndromic X-linked intellectual disability\",\"id\":\"DOID:0050776\"}]" }, { "gene_id": 245684, "description": "connector enhancer of kinase suppressor of Ras 2", "gene_symbol": "[\"Cnksr2\"]", "do": null }, { "gene_id": 245688, "description": "retinoblastoma binding protein 7, chromatin remodeling factor", "gene_symbol": "[\"Rbbp7\"]", "do": null }, { "gene_id": 245827, "description": "FAT atypical cadherin 2", "gene_symbol": "[\"Fat2\"]", "do": null }, { "gene_id": 245860, "description": "autophagy related 9A", "gene_symbol": "[\"Atg9a\"]", "do": null }, { "gene_id": 245865, "description": "sperm associated antigen 4", "gene_symbol": "[\"Spag4\"]", "do": null }, { "gene_id": 245877, "description": "MAP7 domain containing 1", "gene_symbol": "[\"Map7d1\"]", "do": null }, { "gene_id": 245880, "description": "WASP family, member 3", "gene_symbol": "[\"Wasf3\"]", "do": null }, { "gene_id": 245945, "description": "RNA binding motif protein 47", "gene_symbol": "[\"Rbm47\"]", "do": null }, { "gene_id": 246048, "description": "chondrolectin", "gene_symbol": "[\"Chodl\"]", "do": null }, { "gene_id": 246103, "description": "ataxin 7", "gene_symbol": "[\"Atxn7\"]", "do": "[{\"label\":\"spinocerebellar ataxia 7\",\"id\":\"DOID:0050958\"}]" }, { "gene_id": 246133, "description": "potassium voltage-gated channel, Isk-related subfamily, gene 2", "gene_symbol": "[\"Kcne2\"]", "do": null }, { "gene_id": 246154, "description": "vasorin", "gene_symbol": "[\"Vasn\"]", "do": null }, { "gene_id": 246177, "description": "myosin IG", "gene_symbol": "[\"Myo1g\"]", "do": null }, { "gene_id": 246179, "description": "fukutin", "gene_symbol": "[\"Fktn\"]", "do": "[{\"label\":\"Fukuyama congenital muscular dystrophy\",\"id\":\"DOID:0050559\"},{\"label\":\"muscular dystrophy-dystroglycanopathy type B1\",\"id\":\"DOID:0050588\"}]" }, { "gene_id": 246190, "description": "otoancorin", "gene_symbol": "[\"Otoa\"]", "do": "[{\"label\":\"autosomal recessive nonsyndromic deafness 22\",\"id\":\"DOID:0110480\"}]" }, { "gene_id": 246198, "description": "myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6", "gene_symbol": "[\"Mllt6\"]", "do": null }, { "gene_id": 246228, "description": "von Willebrand factor A domain containing 1", "gene_symbol": "[\"Vwa1\"]", "do": null }, { "gene_id": 246256, "description": "Fc receptor, IgG, low affinity IV", "gene_symbol": "[\"Fcgr4\"]", "do": null }, { "gene_id": 246278, "description": "CD207 antigen", "gene_symbol": "[\"Cd207\"]", "do": null }, { "gene_id": 246313, "description": "prokineticin receptor 2", "gene_symbol": "[\"Prokr2\"]", "do": null }, { "gene_id": 246316, "description": "leucine-rich repeat LGI family, member 2", "gene_symbol": "[\"Lgi2\"]", "do": null }, { "gene_id": 246317, "description": "neuropilin (NRP) and tolloid (TLL)-like 1", "gene_symbol": "[\"Neto1\"]", "do": null }, { "gene_id": 246707, "description": "elastin microfibril interfacer 2", "gene_symbol": "[\"Emilin2\"]", "do": null }, { "gene_id": 246730, "description": "2'-5' oligoadenylate synthetase 1A", "gene_symbol": "[\"Oas1a\"]", "do": null }, { "gene_id": 246779, "description": "interleukin 27", "gene_symbol": "[\"Il27\"]", "do": null }, { "gene_id": 246787, "description": "solute carrier family 5 (sodium/glucose cotransporter), member 2", "gene_symbol": "[\"Slc5a2\"]", "do": null }, { "gene_id": 252837, "description": "atypical chemokine receptor 4", "gene_symbol": "[\"Ackr4\"]", "do": null }, { "gene_id": 252866, "description": "a disintegrin and metallopeptidase domain 34", "gene_symbol": "[\"Adam34\"]", "do": null }, { "gene_id": 252870, "description": "ubiquitin specific peptidase 7", "gene_symbol": "[\"Usp7\"]", "do": null }, { "gene_id": 252972, "description": "two pore channel 1", "gene_symbol": "[\"Tpcn1\"]", "do": null }, { "gene_id": 252973, "description": "grainyhead like transcription factor 2", "gene_symbol": "[\"Grhl2\"]", "do": null }, { "gene_id": 252974, "description": "thrombospondin type laminin G domain and EAR repeats", "gene_symbol": "[\"Tspear\"]", "do": null }, { "gene_id": 257630, "description": "interleukin 17F", "gene_symbol": "[\"Il17f\"]", "do": null }, { "gene_id": 257890, "description": "olfactory receptor family 9 subfamily S member 13", "gene_symbol": "[\"Or9s13\"]", "do": null }, { "gene_id": 257898, "description": "olfactory receptor family 7 subfamily D member 11", "gene_symbol": "[\"Or7d11\"]", "do": null }, { "gene_id": 258304, "description": "olfactory receptor family 5 subfamily P member 73", "gene_symbol": "[\"Or5p73\"]", "do": null }, { "gene_id": 258307, "description": "olfactory receptor family 5 subfamily P member 68", "gene_symbol": "[\"Or5p68\"]", "do": null }, { "gene_id": 258308, "description": "olfactory receptor family 5 subfamily P member 81", "gene_symbol": "[\"Or5p81\"]", "do": null }, { "gene_id": 258310, "description": "olfactory receptor family 8 subfamily B member 8", "gene_symbol": "[\"Or8b8\"]", "do": null }, { "gene_id": 258318, "description": "olfactory receptor family 5 subfamily H member 18", "gene_symbol": "[\"Or5h18\"]", "do": null }, { "gene_id": 258327, "description": "olfactory receptor family 10 subfamily D member 3", "gene_symbol": "[\"Or10d3\"]", "do": null }, { "gene_id": 258361, "description": "olfactory receptor family 5 subfamily P member 70", "gene_symbol": "[\"Or5p70\"]", "do": null }, { "gene_id": 258362, "description": "olfactory receptor family 5 subfamily T member 9", "gene_symbol": "[\"Or5t9\"]", "do": null }, { "gene_id": 258417, "description": "olfactory receptor family 5 subfamily P member 51", "gene_symbol": "[\"Or5p51\"]", "do": null }, { "gene_id": 258418, "description": "olfactory receptor family 5 subfamily P member 50", "gene_symbol": "[\"Or5p50\"]", "do": null }, { "gene_id": 258428, "description": "olfactory receptor family 5 subfamily G member 29", "gene_symbol": "[\"Or5g29\"]", "do": null }, { "gene_id": 258488, "description": "olfactory receptor family 5 subfamily P member 54", "gene_symbol": "[\"Or5p54\"]", "do": null }, { "gene_id": 258489, "description": "olfactory receptor family 5 subfamily P member 62", "gene_symbol": "[\"Or5p62\"]", "do": null }, { "gene_id": 258490, "description": "olfactory receptor family 5 subfamily P member 67", "gene_symbol": "[\"Or5p67\"]", "do": null }, { "gene_id": 258491, "description": "olfactory receptor family 5 subfamily P member 66", "gene_symbol": "[\"Or5p66\"]", "do": null }, { "gene_id": 258492, "description": "olfactory receptor family 5 subfamily P member 60", "gene_symbol": "[\"Or5p60\"]", "do": null }, { "gene_id": 258498, "description": "olfactory receptor family 10 subfamily N member 1", "gene_symbol": "[\"Or10n1\"]", "do": null }, { "gene_id": 258565, "description": "olfactory receptor family 5 subfamily G member 9", "gene_symbol": "[\"Or5g9\"]", "do": null }, { "gene_id": 258566, "description": "olfactory receptor family 5 subfamily G member 25", "gene_symbol": "[\"Or5g25\"]", "do": null }, { "gene_id": 258573, "description": "olfactory receptor family 5 subfamily AP member 2", "gene_symbol": "[\"Or5ap2\"]", "do": null }, { "gene_id": 258581, "description": "olfactory receptor family 5 subfamily M member 5", "gene_symbol": "[\"Or5m5\"]", "do": null }, { "gene_id": 258585, "description": "olfactory receptor family 5 subfamily T member 7", "gene_symbol": "[\"Or5t7\"]", "do": null }, { "gene_id": 258602, "description": "olfactory receptor family 8 subfamily G member 50", "gene_symbol": "[\"Or8g50\"]", "do": null }, { "gene_id": 258658, "description": "olfactory receptor family 4 subfamily M member 1", "gene_symbol": "[\"Or4m1\"]", "do": null }, { "gene_id": 258697, "description": "olfactory receptor family 5 subfamily B member 21", "gene_symbol": "[\"Or5b21\"]", "do": null }, { "gene_id": 258703, "description": "olfactory receptor family 3 subfamily A member 1C", "gene_symbol": "[\"Or3a1c\"]", "do": null }, { "gene_id": 258727, "description": "olfactory receptor family 5 subfamily P member 64", "gene_symbol": "[\"Or5p64\"]", "do": null }, { "gene_id": 258728, "description": "olfactory receptor family 5 subfamily P member 58", "gene_symbol": "[\"Or5p58\"]", "do": null }, { "gene_id": 258729, "description": "olfactory receptor family 5 subfamily P member 6", "gene_symbol": "[\"Or5p6\"]", "do": null }, { "gene_id": 258730, "description": "olfactory receptor family 5 subfamily P member 59", "gene_symbol": "[\"Or5p59\"]", "do": null }, { "gene_id": 258731, "description": "olfactory receptor family 5 subfamily P member 1", "gene_symbol": "[\"Or5p1\"]", "do": null }, { "gene_id": 258732, "description": "olfactory receptor family 5 subfamily P member 69", "gene_symbol": "[\"Or5p69\"]", "do": null }, { "gene_id": 258733, "description": "olfactory receptor family 5 subfamily P member 72", "gene_symbol": "[\"Or5p72\"]", "do": null }, { "gene_id": 258734, "description": "olfactory receptor family 5 subfamily P member 76", "gene_symbol": "[\"Or5p76\"]", "do": null }, { "gene_id": 258738, "description": "olfactory receptor family 5 subfamily P member 79", "gene_symbol": "[\"Or5p79\"]", "do": null }, { "gene_id": 258742, "description": "olfactory receptor family 8 subfamily G member 17", "gene_symbol": "[\"Or8g17\"]", "do": null }, { "gene_id": 258769, "description": "olfactory receptor family 5 subfamily P member 80", "gene_symbol": "[\"Or5p80\"]", "do": null }, { "gene_id": 258770, "description": "olfactory receptor family 5 subfamily P member 52", "gene_symbol": "[\"Or5p52\"]", "do": null }, { "gene_id": 258771, "description": "olfactory receptor family 5 subfamily P member 53", "gene_symbol": "[\"Or5p53\"]", "do": null }, { "gene_id": 258869, "description": "olfactory receptor family 8 subfamily B member 3", "gene_symbol": "[\"Or8b3\"]", "do": null }, { "gene_id": 258923, "description": "olfactory receptor family 1 subfamily E member 16", "gene_symbol": "[\"Or1e16\"]", "do": null }, { "gene_id": 258926, "description": "olfactory receptor family 5 subfamily P member 55", "gene_symbol": "[\"Or5p55\"]", "do": null }, { "gene_id": 258927, "description": "olfactory receptor family 5 subfamily P member 4", "gene_symbol": "[\"Or5p4\"]", "do": null }, { "gene_id": 258928, "description": "olfactory receptor family 5 subfamily P member 56", "gene_symbol": "[\"Or5p56\"]", "do": null }, { "gene_id": 258939, "description": "olfactory receptor family 10 subfamily H member 28", "gene_symbol": "[\"Or10h28\"]", "do": null }, { "gene_id": 259001, "description": "olfactory receptor family 5 subfamily K member 17", "gene_symbol": "[\"Or5k17\"]", "do": null }, { "gene_id": 259005, "description": "olfactory receptor family 3 subfamily A member 10", "gene_symbol": "[\"Or3a10\"]", "do": null }, { "gene_id": 259012, "description": "olfactory receptor family 5 subfamily J member 3", "gene_symbol": "[\"Or5j3\"]", "do": null }, { "gene_id": 259013, "description": "olfactory receptor family 8 subfamily U member 9", "gene_symbol": "[\"Or8u9\"]", "do": null }, { "gene_id": 259015, "description": "olfactory receptor family 8 subfamily U member 3", "gene_symbol": "[\"Or8u3\"]", "do": null }, { "gene_id": 259017, "description": "olfactory receptor family 5 subfamily AR member 1", "gene_symbol": "[\"Or5ar1\"]", "do": null }, { "gene_id": 259172, "description": "membrane frizzled-related protein", "gene_symbol": "[\"Mfrp\"]", "do": "[{\"label\":\"fundus albipunctatus\",\"id\":\"DOID:11105\"}]" }, { "gene_id": 259277, "description": "kallikrein related-peptidase 8", "gene_symbol": "[\"Klk8\"]", "do": null }, { "gene_id": 259279, "description": "tubulin, gamma complex component 3", "gene_symbol": "[\"Tubgcp3\"]", "do": null }, { "gene_id": 259302, "description": "SLIT-ROBO Rho GTPase activating protein 3", "gene_symbol": "[\"Srgap3\"]", "do": "[{\"label\":\"schizophrenia\",\"id\":\"DOID:5419\"}]" }, { "gene_id": 260296, "description": "tripartite motif-containing 61", "gene_symbol": "[\"Trim61\"]", "do": null }, { "gene_id": 260299, "description": "cell adhesion molecule 4", "gene_symbol": "[\"Cadm4\"]", "do": null }, { "gene_id": 260302, "description": "golgi associated, gamma adaptin ear containing, ARF binding protein 3", "gene_symbol": "[\"Gga3\"]", "do": null }, { "gene_id": 260305, "description": "nephronophthisis 4 (juvenile) homolog (human)", "gene_symbol": "[\"Nphp4\"]", "do": null }, { "gene_id": 260315, "description": "neuron navigator 3", "gene_symbol": "[\"Nav3\"]", "do": null }, { "gene_id": 260408, "description": "serine protease 45", "gene_symbol": "[\"Prss45\"]", "do": null }, { "gene_id": 263764, "description": "cellular repressor of E1A-stimulated genes 2", "gene_symbol": "[\"Creg2\"]", "do": null }, { "gene_id": 263876, "description": "spermatogenesis associated 2", "gene_symbol": "[\"Spata2\"]", "do": null }, { "gene_id": 264064, "description": "cyclin dependent kinase 8", "gene_symbol": "[\"Cdk8\"]", "do": null }, { "gene_id": 266614, "description": "lymphocyte antigen 6 family member G5B", "gene_symbol": "[\"Ly6g5b\"]", "do": null }, { "gene_id": 266690, "description": "cytochrome b5 reductase 4", "gene_symbol": "[\"Cyb5r4\"]", "do": "[{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 266692, "description": "copine I", "gene_symbol": "[\"Cpne1\"]", "do": null }, { "gene_id": 266815, "description": "MHC I like leukocyte 1", "gene_symbol": "[\"Mill1\"]", "do": null }, { "gene_id": 268301, "description": "sosondowah ankyrin repeat domain family member C", "gene_symbol": "[\"Sowahc\"]", "do": null }, { "gene_id": 268345, "description": "potassium voltage gated channel, Shaw-related subfamily, member 2", "gene_symbol": "[\"Kcnc2\"]", "do": null }, { "gene_id": 268373, "description": "peptidylprolyl isomerase A", "gene_symbol": "[\"Ppia\"]", "do": null }, { "gene_id": 268379, "description": "ATP-binding cassette, sub-family A member 13", "gene_symbol": "[\"Abca13\"]", "do": null }, { "gene_id": 268395, "description": "N-methylpurine-DNA glycosylase", "gene_symbol": "[\"Mpg\"]", "do": null }, { "gene_id": 268396, "description": "SH3 and PX domains 2B", "gene_symbol": "[\"Sh3pxd2b\"]", "do": "[{\"label\":\"glaucoma\",\"id\":\"DOID:1686\"},{\"label\":\"otitis media\",\"id\":\"DOID:10754\"}]" }, { "gene_id": 268448, "description": "PHD finger protein 12", "gene_symbol": "[\"Phf12\"]", "do": null }, { "gene_id": 268465, "description": "essential meiotic structure-specific endonuclease 1", "gene_symbol": "[\"Eme1\"]", "do": null }, { "gene_id": 268510, "description": "mannoside acetylglucosaminyltransferase 5, isoenzyme B", "gene_symbol": "[\"Mgat5b\"]", "do": null }, { "gene_id": 268512, "description": "solute carrier family 26, member 11", "gene_symbol": "[\"Slc26a11\"]", "do": null }, { "gene_id": 268515, "description": "BAH domain and coiled-coil containing 1", "gene_symbol": "[\"Bahcc1\"]", "do": null }, { "gene_id": 268566, "description": "gephyrin", "gene_symbol": "[\"Gphn\"]", "do": null }, { "gene_id": 268591, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 5", "gene_symbol": "[\"Serpina5\"]", "do": null }, { "gene_id": 268663, "description": "cadherin-related family member 2", "gene_symbol": "[\"Cdhr2\"]", "do": null }, { "gene_id": 268697, "description": "cyclin B1", "gene_symbol": "[\"Ccnb1\"]", "do": null }, { "gene_id": 268706, "description": "solute carrier family 38, member 9", "gene_symbol": "[\"Slc38a9\"]", "do": null }, { "gene_id": 268721, "description": "zinc finger SWIM-type containing 8", "gene_symbol": "[\"Zswim8\"]", "do": null }, { "gene_id": 268739, "description": "Rho guanine nucleotide exchange factor 40", "gene_symbol": "[\"Arhgef40\"]", "do": null }, { "gene_id": 268741, "description": "TOX high mobility group box family member 4", "gene_symbol": "[\"Tox4\"]", "do": null }, { "gene_id": 268747, "description": "capping protein regulator and myosin 1 linker 3", "gene_symbol": "[\"Carmil3\"]", "do": null }, { "gene_id": 268756, "description": "gulonolactone (L-) oxidase", "gene_symbol": "[\"Gulo\"]", "do": null }, { "gene_id": 268759, "description": "RIKEN cDNA 9930012K11 gene", "gene_symbol": "[\"9930012K11Rik\"]", "do": null }, { "gene_id": 268780, "description": "EGF-like, fibronectin type III and laminin G domains", "gene_symbol": "[\"Egflam\"]", "do": null }, { "gene_id": 268782, "description": "alanine-glyoxylate aminotransferase 2", "gene_symbol": "[\"Agxt2\"]", "do": null }, { "gene_id": 268859, "description": "RNA binding protein, fox-1 homolog (C. elegans) 1", "gene_symbol": "[\"Rbfox1\"]", "do": null }, { "gene_id": 268878, "description": "ATPase type 13A5", "gene_symbol": "[\"Atp13a5\"]", "do": null }, { "gene_id": 268880, "description": "xyloside xylosyltransferase 1", "gene_symbol": "[\"Xxylt1\"]", "do": null }, { "gene_id": 268890, "description": "limbic system-associated membrane protein", "gene_symbol": "[\"Lsamp\"]", "do": null }, { "gene_id": 268902, "description": "roundabout guidance receptor 2", "gene_symbol": "[\"Robo2\"]", "do": null }, { "gene_id": 268932, "description": "CASK interacting protein 1", "gene_symbol": "[\"Caskin1\"]", "do": null }, { "gene_id": 268934, "description": "glutamate receptor, metabotropic 4", "gene_symbol": "[\"Grm4\"]", "do": null }, { "gene_id": 268935, "description": "signal peptide, CUB domain, EGF-like 3", "gene_symbol": "[\"Scube3\"]", "do": null }, { "gene_id": 268949, "description": "mucin like 3", "gene_symbol": "[\"Mucl3\"]", "do": null }, { "gene_id": 268970, "description": "Rho GTPase activating protein 28", "gene_symbol": "[\"Arhgap28\"]", "do": null }, { "gene_id": 268977, "description": "latent transforming growth factor beta binding protein 1", "gene_symbol": "[\"Ltbp1\"]", "do": null }, { "gene_id": 268980, "description": "striatin, calmodulin binding protein", "gene_symbol": "[\"Strn\"]", "do": null }, { "gene_id": 269003, "description": "Sin3A associated protein 130", "gene_symbol": "[\"Sap130\"]", "do": "[{\"label\":\"congenital heart disease\",\"id\":\"DOID:1682\"},{\"label\":\"hypoplastic left heart syndrome\",\"id\":\"DOID:9955\"}]" }, { "gene_id": 269023, "description": "zinc finger protein 608", "gene_symbol": "[\"Zfp608\"]", "do": null }, { "gene_id": 269060, "description": "diacylglycerol lipase, alpha", "gene_symbol": "[\"Dagla\"]", "do": null }, { "gene_id": 269109, "description": "dipeptidylpeptidase 10", "gene_symbol": "[\"Dpp10\"]", "do": null }, { "gene_id": 269113, "description": "nucleoporin 54", "gene_symbol": "[\"Nup54\"]", "do": null }, { "gene_id": 269116, "description": "neurofascin", "gene_symbol": "[\"Nfasc\"]", "do": null }, { "gene_id": 269120, "description": "opticin", "gene_symbol": "[\"Optc\"]", "do": null }, { "gene_id": 269132, "description": "collagen beta(1-O)galactosyltransferase 2", "gene_symbol": "[\"Colgalt2\"]", "do": null }, { "gene_id": 269180, "description": "inositol polyphosphate-4-phosphatase, type I", "gene_symbol": "[\"Inpp4a\"]", "do": null }, { "gene_id": 269181, "description": "mannoside acetylglucosaminyltransferase 4, isoenzyme A", "gene_symbol": "[\"Mgat4a\"]", "do": null }, { "gene_id": 269233, "description": "family with sequence similarity 171, member A1", "gene_symbol": "[\"Fam171a1\"]", "do": null }, { "gene_id": 269254, "description": "senataxin", "gene_symbol": "[\"Setx\"]", "do": "[{\"label\":\"amyotrophic lateral sclerosis type 4\",\"id\":\"DOID:0060196\"}]" }, { "gene_id": 269261, "description": "ribosomal protein L12", "gene_symbol": "[\"Rpl12\"]", "do": null }, { "gene_id": 269295, "description": "reticulon 4 receptor-like 2", "gene_symbol": "[\"Rtn4rl2\"]", "do": null }, { "gene_id": 269328, "description": "mucin 15", "gene_symbol": "[\"Muc15\"]", "do": null }, { "gene_id": 269346, "description": "solute carrier family 28 (sodium-coupled nucleoside transporter), member 2", "gene_symbol": "[\"Slc28a2\"]", "do": null }, { "gene_id": 269356, "description": "solute carrier family 4, sodium bicarbonate transporter-like, member 11", "gene_symbol": "[\"Slc4a11\"]", "do": "[{\"label\":\"congenital hereditary endothelial dystrophy of cornea\",\"id\":\"DOID:0060649\"}]" }, { "gene_id": 269378, "description": "S-adenosylhomocysteine hydrolase", "gene_symbol": "[\"Ahcy\"]", "do": null }, { "gene_id": 269397, "description": "SS18, nBAF chromatin remodeling complex subunit like 1", "gene_symbol": "[\"Ss18l1\"]", "do": null }, { "gene_id": 269423, "description": "abhydrolase domain containing 18", "gene_symbol": "[\"Abhd18\"]", "do": null }, { "gene_id": 269473, "description": "leucine-rich repeats and immunoglobulin-like domains 2", "gene_symbol": "[\"Lrig2\"]", "do": null }, { "gene_id": 269529, "description": "F-box protein 10", "gene_symbol": "[\"Fbxo10\"]", "do": null }, { "gene_id": 269587, "description": "erythrocyte membrane protein band 4.1", "gene_symbol": "[\"Epb41\"]", "do": null }, { "gene_id": 269593, "description": "leucine zipper protein 1", "gene_symbol": "[\"Luzp1\"]", "do": null }, { "gene_id": 269639, "description": "zinc finger protein 512", "gene_symbol": "[\"Zfp512\"]", "do": null }, { "gene_id": 269682, "description": "golgin A3", "gene_symbol": "[\"Golga3\"]", "do": null }, { "gene_id": 269701, "description": "cilia and flagella associated protein 251", "gene_symbol": "[\"Cfap251\"]", "do": null }, { "gene_id": 269713, "description": "CAP-GLY domain containing linker protein 2", "gene_symbol": "[\"Clip2\"]", "do": "[{\"label\":\"Williams-Beuren syndrome\",\"id\":\"DOID:1928\"}]" }, { "gene_id": 269774, "description": "AP2 associated kinase 1", "gene_symbol": "[\"Aak1\"]", "do": null }, { "gene_id": 269784, "description": "contactin 4", "gene_symbol": "[\"Cntn4\"]", "do": null }, { "gene_id": 269788, "description": "lipoma HMGIC fusion partner-like protein 4", "gene_symbol": "[\"Lhfpl4\"]", "do": null }, { "gene_id": 269800, "description": "zinc finger protein 384", "gene_symbol": "[\"Zfp384\"]", "do": null }, { "gene_id": 269823, "description": "paraoxonase 3", "gene_symbol": "[\"Pon3\"]", "do": null }, { "gene_id": 269855, "description": "scavenger receptor cysteine rich family, 5 domains", "gene_symbol": "[\"Ssc5d\"]", "do": null }, { "gene_id": 269878, "description": "multiple EGF-like-domains 8", "gene_symbol": "[\"Megf8\"]", "do": "[{\"label\":\"Carpenter syndrome\",\"id\":\"DOID:0060234\"},{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 269881, "description": "mitogen-activated protein kinase kinase kinase 10", "gene_symbol": "[\"Map3k10\"]", "do": null }, { "gene_id": 269941, "description": "chondroitin sulfate synthase 1", "gene_symbol": "[\"Chsy1\"]", "do": null }, { "gene_id": 269951, "description": "isocitrate dehydrogenase 2 (NADP+), mitochondrial", "gene_symbol": "[\"Idh2\"]", "do": "[{\"label\":\"bone remodeling disease\",\"id\":\"DOID:0080005\"}]" }, { "gene_id": 269952, "description": "GDP-D-glucose phosphorylase 1", "gene_symbol": "[\"Gdpgp1\"]", "do": null }, { "gene_id": 269959, "description": "ADAMTS-like 3", "gene_symbol": "[\"Adamtsl3\"]", "do": null }, { "gene_id": 269966, "description": "nucleoporin 98", "gene_symbol": "[\"Nup98\"]", "do": null }, { "gene_id": 270028, "description": "NALCN channel auxiliary factor 1", "gene_symbol": "[\"Nalf1\"]", "do": null }, { "gene_id": 270035, "description": "leucine zipper-EF-hand containing transmembrane protein 2", "gene_symbol": "[\"Letm2\"]", "do": null }, { "gene_id": 270049, "description": "UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 6", "gene_symbol": "[\"Galntl6\"]", "do": null }, { "gene_id": 270058, "description": "microtubule-associated protein 1S", "gene_symbol": "[\"Map1s\"]", "do": null }, { "gene_id": 270109, "description": "pecanex homolog 2", "gene_symbol": "[\"Pcnx2\"]", "do": null }, { "gene_id": 270110, "description": "interferon regulatory factor 2 binding protein 2", "gene_symbol": "[\"Irf2bp2\"]", "do": null }, { "gene_id": 270120, "description": "FAT atypical cadherin 3", "gene_symbol": "[\"Fat3\"]", "do": null }, { "gene_id": 270151, "description": "NLR family member X1", "gene_symbol": "[\"Nlrx1\"]", "do": null }, { "gene_id": 270152, "description": "junction adhesion molecule like", "gene_symbol": "[\"Jaml\"]", "do": null }, { "gene_id": 270163, "description": "myosin IXa", "gene_symbol": "[\"Myo9a\"]", "do": "[{\"label\":\"focal segmental glomerulosclerosis\",\"id\":\"DOID:1312\"},{\"label\":\"obstructive hydrocephalus\",\"id\":\"DOID:14159\"}]" }, { "gene_id": 270190, "description": "Eph receptor B1", "gene_symbol": "[\"Ephb1\"]", "do": null }, { "gene_id": 270198, "description": "6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4", "gene_symbol": "[\"Pfkfb4\"]", "do": null }, { "gene_id": 270627, "description": "TATA-box binding protein associated factor 1", "gene_symbol": "[\"Taf1\"]", "do": null }, { "gene_id": 270669, "description": "membrane-bound transcription factor peptidase, site 2", "gene_symbol": "[\"Mbtps2\"]", "do": null }, { "gene_id": 270672, "description": "mitogen-activated protein kinase kinase kinase 15", "gene_symbol": "[\"Map3k15\"]", "do": null }, { "gene_id": 270757, "description": "BPI fold containing family C", "gene_symbol": "[\"Bpifc\"]", "do": null }, { "gene_id": 270893, "description": "transmembrane protein 132E", "gene_symbol": "[\"Tmem132e\"]", "do": null }, { "gene_id": 271036, "description": "cation channel sperm associated auxiliary subunit beta", "gene_symbol": "[\"Catsperb\"]", "do": null }, { "gene_id": 271047, "description": "serine (or cysteine) peptidase inhibitor, clade A, member 3B", "gene_symbol": "[\"Serpina3b\"]", "do": null }, { "gene_id": 271127, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 16", "gene_symbol": "[\"Adamts16\"]", "do": null }, { "gene_id": 271375, "description": "Cd200 receptor 2", "gene_symbol": "[\"Cd200r2\"]", "do": null }, { "gene_id": 271564, "description": "vacuolar protein sorting 13A", "gene_symbol": "[\"Vps13a\"]", "do": "[{\"label\":\"choreaacanthocytosis\",\"id\":\"DOID:0050766\"}]" }, { "gene_id": 271639, "description": "adenylate cyclase 10", "gene_symbol": "[\"Adcy10\"]", "do": null }, { "gene_id": 271786, "description": "polypeptide N-acetylgalactosaminyltransferase 13", "gene_symbol": "[\"Galnt13\"]", "do": null }, { "gene_id": 271813, "description": "ATP/GTP binding protein-like 2", "gene_symbol": "[\"Agbl2\"]", "do": null }, { "gene_id": 271970, "description": "arylsulfatase J", "gene_symbol": "[\"Arsj\"]", "do": null }, { "gene_id": 272031, "description": "phospholipid phosphatase related 1", "gene_symbol": "[\"Plppr1\"]", "do": null }, { "gene_id": 272381, "description": "leucine rich repeat containing 4B", "gene_symbol": "[\"Lrrc4b\"]", "do": null }, { "gene_id": 272411, "description": "UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6", "gene_symbol": "[\"B3gnt6\"]", "do": null }, { "gene_id": 276742, "description": "trace amine-associated receptor 7E", "gene_symbol": "[\"Taar7e\"]", "do": null }, { "gene_id": 276846, "description": "phosphatidylinositol glycan anchor biosynthesis, class S", "gene_symbol": "[\"Pigs\"]", "do": null }, { "gene_id": 276891, "description": "T cell immunoglobulin and mucin domain containing 4", "gene_symbol": "[\"Timd4\"]", "do": "[{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 276920, "description": "coiled-coil domain containing 42", "gene_symbol": "[\"Ccdc42\"]", "do": null }, { "gene_id": 277154, "description": "NYN domain and retroviral integrase containing", "gene_symbol": "[\"Nynrin\"]", "do": null }, { "gene_id": 277203, "description": "transmembrane 4 L six family member 19", "gene_symbol": "[\"Tm4sf19\"]", "do": null }, { "gene_id": 277250, "description": "KDM3B lysine (K)-specific demethylase 3B", "gene_symbol": "[\"Kdm3b\"]", "do": null }, { "gene_id": 277328, "description": "transient receptor potential cation channel, subfamily A, member 1", "gene_symbol": "[\"Trpa1\"]", "do": null }, { "gene_id": 277360, "description": "phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1", "gene_symbol": "[\"Prex1\"]", "do": null }, { "gene_id": 277463, "description": "G protein-coupled receptor 107", "gene_symbol": "[\"Gpr107\"]", "do": null }, { "gene_id": 277468, "description": "solute carrier family 39 (zinc transporter), member 12", "gene_symbol": "[\"Slc39a12\"]", "do": null }, { "gene_id": 277854, "description": "DEP domain containing 5", "gene_symbol": "[\"Depdc5\"]", "do": null }, { "gene_id": 277939, "description": "C2 calcium-dependent domain containing 3", "gene_symbol": "[\"C2cd3\"]", "do": null }, { "gene_id": 278203, "description": "sperm acrosome associated 5", "gene_symbol": "[\"Spaca5\"]", "do": null }, { "gene_id": 278279, "description": "transmembrane and tetratricopeptide repeat containing 2", "gene_symbol": "[\"Tmtc2\"]", "do": null }, { "gene_id": 278507, "description": "WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2", "gene_symbol": "[\"Wfikkn2\"]", "do": null }, { "gene_id": 279028, "description": "ADAM metallopeptidase with thrombospondin type 1 motif 13", "gene_symbol": "[\"Adamts13\"]", "do": null }, { "gene_id": 279561, "description": "WNK lysine deficient protein kinase 3", "gene_symbol": "[\"Wnk3\"]", "do": null }, { "gene_id": 279572, "description": "toll-like receptor 13", "gene_symbol": "[\"Tlr13\"]", "do": null }, { "gene_id": 279653, "description": "protocadherin 19", "gene_symbol": "[\"Pcdh19\"]", "do": null }, { "gene_id": 280635, "description": "elastin microfibril interfacer 3", "gene_symbol": "[\"Emilin3\"]", "do": null }, { "gene_id": 280645, "description": "beta-1,3-glucuronyltransferase 2", "gene_symbol": "[\"B3gat2\"]", "do": null }, { "gene_id": 280662, "description": "afamin", "gene_symbol": "[\"Afm\"]", "do": null }, { "gene_id": 280667, "description": "a disintegrin and metallopeptidase domain 1b", "gene_symbol": "[\"Adam1b\"]", "do": null }, { "gene_id": 280668, "description": "a disintegrin and metallopeptidase domain 1a", "gene_symbol": "[\"Adam1a\"]", "do": null }, { "gene_id": 286940, "description": "filamin, beta", "gene_symbol": "[\"Flnb\"]", "do": "[{\"label\":\"spondylocarpotarsal synostosis syndrome\",\"id\":\"DOID:0090116\"}]" }, { "gene_id": 317677, "description": "complement component 1, s subcomponent 2", "gene_symbol": "[\"C1s2\"]", "do": null }, { "gene_id": 319155, "description": "H4 clustered histone 3", "gene_symbol": "[\"H4c3\"]", "do": null }, { "gene_id": 319156, "description": "H4 clustered histone 4", "gene_symbol": "[\"H4c4\"]", "do": null }, { "gene_id": 319157, "description": "H4 clustered histone 6", "gene_symbol": "[\"H4c6\"]", "do": null }, { "gene_id": 319158, "description": "H4 clustered histone 9", "gene_symbol": "[\"H4c9\"]", "do": null }, { "gene_id": 319159, "description": "H4 clustered histone 11", "gene_symbol": "[\"H4c11\"]", "do": null }, { "gene_id": 319160, "description": "H4 clustered histone 12", "gene_symbol": "[\"H4c12\"]", "do": null }, { "gene_id": 319161, "description": "H4 clustered histone 18", "gene_symbol": "[\"H4c18\"]", "do": null }, { "gene_id": 319162, "description": "H2A clustered histone 25", "gene_symbol": "[\"H2ac25\"]", "do": null }, { "gene_id": 319178, "description": "H2B clustered histone 3", "gene_symbol": "[\"H2bc3\"]", "do": null }, { "gene_id": 319179, "description": "H2B clustered histone 6", "gene_symbol": "[\"H2bc6\"]", "do": null }, { "gene_id": 319180, "description": "H2B clustered histone 7", "gene_symbol": "[\"H2bc7\"]", "do": null }, { "gene_id": 319181, "description": "H2B clustered histone 8", "gene_symbol": "[\"H2bc8\"]", "do": null }, { "gene_id": 319182, "description": "H2B clustered histone 9", "gene_symbol": "[\"H2bc9\"]", "do": null }, { "gene_id": 319183, "description": "H2B clustered histone 11", "gene_symbol": "[\"H2bc11\"]", "do": null }, { "gene_id": 319184, "description": "H2B clustered histone 12", "gene_symbol": "[\"H2bc12\"]", "do": null }, { "gene_id": 319185, "description": "H2B clustered histone 13", "gene_symbol": "[\"H2bc13\"]", "do": null }, { "gene_id": 319186, "description": "H2B clustered histone 14", "gene_symbol": "[\"H2bc14\"]", "do": null }, { "gene_id": 319187, "description": "H2B clustered histone 15", "gene_symbol": "[\"H2bc15\"]", "do": null }, { "gene_id": 319188, "description": "H2B clustered histone 22", "gene_symbol": "[\"H2bc22\"]", "do": null }, { "gene_id": 319189, "description": "H2B clustered histone 18", "gene_symbol": "[\"H2bc18\"]", "do": null }, { "gene_id": 319190, "description": "H2B clustered histone 21", "gene_symbol": "[\"H2bc21\"]", "do": null }, { "gene_id": 319197, "description": "G protein-coupled receptor 4", "gene_symbol": "[\"Gpr4\"]", "do": null }, { "gene_id": 319200, "description": "G protein-coupled receptor 82", "gene_symbol": "[\"Gpr82\"]", "do": null }, { "gene_id": 319229, "description": "secretin receptor", "gene_symbol": "[\"Sctr\"]", "do": null }, { "gene_id": 319239, "description": "neuropeptide S receptor 1", "gene_symbol": "[\"Npsr1\"]", "do": "[{\"label\":\"sleep disorder\",\"id\":\"DOID:535\"}]" }, { "gene_id": 319277, "description": "WASH complex subunit 4", "gene_symbol": "[\"Washc4\"]", "do": "[{\"label\":\"Wiskott-Aldrich syndrome\",\"id\":\"DOID:9169\"}]" }, { "gene_id": 319322, "description": "splicing factor 3b, subunit 2", "gene_symbol": "[\"Sf3b2\"]", "do": null }, { "gene_id": 319352, "description": "PILR alpha associated neural protein", "gene_symbol": "[\"Pianp\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 319387, "description": "adhesion G protein-coupled receptor L3", "gene_symbol": "[\"Adgrl3\"]", "do": "[{\"label\":\"attention deficit hyperactivity disorder\",\"id\":\"DOID:1094\"}]" }, { "gene_id": 319415, "description": "heparan sulfate (glucosamine) 3-O-sulfotransferase 5", "gene_symbol": "[\"Hs3st5\"]", "do": null }, { "gene_id": 319430, "description": "complement component 5a receptor 2", "gene_symbol": "[\"C5ar2\"]", "do": null }, { "gene_id": 319446, "description": "dipeptidase 2", "gene_symbol": "[\"Dpep2\"]", "do": null }, { "gene_id": 319455, "description": "phospholipase D family member 5", "gene_symbol": "[\"Pld5\"]", "do": null }, { "gene_id": 319476, "description": "leucine-rich repeats and transmembrane domains 1", "gene_symbol": "[\"Lrtm1\"]", "do": null }, { "gene_id": 319482, "description": "Fc fragment of IgG binding protein like 1", "gene_symbol": "[\"Fcgbpl1\"]", "do": null }, { "gene_id": 319504, "description": "neuronal cell adhesion molecule", "gene_symbol": "[\"Nrcam\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 319530, "description": "zinc finger protein 750", "gene_symbol": "[\"Zfp750\"]", "do": null }, { "gene_id": 319535, "description": "zinc finger protein 182", "gene_symbol": "[\"Zfp182\"]", "do": null }, { "gene_id": 319554, "description": "isopentenyl-diphosphate delta isomerase", "gene_symbol": "[\"Idi1\"]", "do": null }, { "gene_id": 319565, "description": "spectrin repeat containing, nuclear envelope 2", "gene_symbol": "[\"Syne2\"]", "do": null }, { "gene_id": 319604, "description": "family with sequence similarity 168, member A", "gene_symbol": "[\"Fam168a\"]", "do": null }, { "gene_id": 319625, "description": "galactose mutarotase", "gene_symbol": "[\"Galm\"]", "do": null }, { "gene_id": 319655, "description": "podocalyxin-like 2", "gene_symbol": "[\"Podxl2\"]", "do": null }, { "gene_id": 319660, "description": "alkylglycerol monooxygenase", "gene_symbol": "[\"Agmo\"]", "do": null }, { "gene_id": 319713, "description": "actin binding LIM protein family, member 3", "gene_symbol": "[\"Ablim3\"]", "do": null }, { "gene_id": 319734, "description": "calcium channel, voltage-dependent, alpha 2/delta subunit 4", "gene_symbol": "[\"Cacna2d4\"]", "do": null }, { "gene_id": 319742, "description": "myelin protein zero-like 3", "gene_symbol": "[\"Mpzl3\"]", "do": null }, { "gene_id": 319748, "description": "zinc finger protein 865", "gene_symbol": "[\"Zfp865\"]", "do": null }, { "gene_id": 319757, "description": "smoothened, frizzled class receptor", "gene_symbol": "[\"Smo\"]", "do": "[{\"label\":\"medulloblastoma\",\"id\":\"DOID:0050902\"},{\"label\":\"pulmonary emphysema\",\"id\":\"DOID:9675\"}]" }, { "gene_id": 319764, "description": "serine rich and transmembrane domain containing 2", "gene_symbol": "[\"Sertm2\"]", "do": null }, { "gene_id": 319800, "description": "solute carrier family 22, member 30", "gene_symbol": "[\"Slc22a30\"]", "do": null }, { "gene_id": 319804, "description": "glycosyltransferase 1 domain containing 1", "gene_symbol": "[\"Glt1d1\"]", "do": null }, { "gene_id": 319817, "description": "ring finger and CCCH-type zinc finger domains 2", "gene_symbol": "[\"Rc3h2\"]", "do": null }, { "gene_id": 319823, "description": "CD200 receptor 1 like", "gene_symbol": "[\"Cd200r1l\"]", "do": null }, { "gene_id": 319845, "description": "Bardet-Biedl syndrome 9", "gene_symbol": "[\"Bbs9\"]", "do": null }, { "gene_id": 319848, "description": "solute carrier family 17 (sodium phosphate), member 4", "gene_symbol": "[\"Slc17a4\"]", "do": null }, { "gene_id": 319875, "description": "transmembrane protease, serine 11B", "gene_symbol": "[\"Tmprss11b\"]", "do": null }, { "gene_id": 319876, "description": "Cobl-like 1", "gene_symbol": "[\"Cobll1\"]", "do": null }, { "gene_id": 319899, "description": "dedicator of cytokinesis 6", "gene_symbol": "[\"Dock6\"]", "do": null }, { "gene_id": 319901, "description": "dermatan sulfate epimerase-like", "gene_symbol": "[\"Dsel\"]", "do": null }, { "gene_id": 319939, "description": "tensin 3", "gene_symbol": "[\"Tns3\"]", "do": null }, { "gene_id": 319996, "description": "golgi membrane protein 2", "gene_symbol": "[\"Golm2\"]", "do": null }, { "gene_id": 320007, "description": "SID1 transmembrane family, member 1", "gene_symbol": "[\"Sidt1\"]", "do": null }, { "gene_id": 320011, "description": "UDP-glucose glycoprotein glucosyltransferase 1", "gene_symbol": "[\"Uggt1\"]", "do": null }, { "gene_id": 320024, "description": "neutral cholesterol ester hydrolase 1", "gene_symbol": "[\"Nceh1\"]", "do": null }, { "gene_id": 320027, "description": "follistatin-like 4", "gene_symbol": "[\"Fstl4\"]", "do": null }, { "gene_id": 320078, "description": "olfactomedin-like 2B", "gene_symbol": "[\"Olfml2b\"]", "do": null }, { "gene_id": 320091, "description": "anoctamin 4", "gene_symbol": "[\"Ano4\"]", "do": null }, { "gene_id": 320095, "description": "RIKEN cDNA 6430550D23 gene", "gene_symbol": "[\"6430550D23Rik\"]", "do": null }, { "gene_id": 320100, "description": "RELT tumor necrosis factor receptor", "gene_symbol": "[\"Relt\"]", "do": "[{\"label\":\"amelogenesis imperfecta type 3C\",\"id\":\"DOID:0111722\"}]" }, { "gene_id": 320106, "description": "solute carrier family 38, member 11", "gene_symbol": "[\"Slc38a11\"]", "do": null }, { "gene_id": 320129, "description": "G protein-coupled receptor kinase 3", "gene_symbol": "[\"Grk3\"]", "do": null }, { "gene_id": 320165, "description": "transforming, acidic coiled-coil containing protein 1", "gene_symbol": "[\"Tacc1\"]", "do": null }, { "gene_id": 320181, "description": "fibronectin type III domain containing 7", "gene_symbol": "[\"Fndc7\"]", "do": null }, { "gene_id": 320202, "description": "left-right determination factor 2", "gene_symbol": "[\"Lefty2\"]", "do": null }, { "gene_id": 320225, "description": "cation channel sperm associated auxiliary subunit gamma 1", "gene_symbol": "[\"Catsperg1\"]", "do": null }, { "gene_id": 320234, "description": "coiled-coil domain containing 66", "gene_symbol": "[\"Ccdc66\"]", "do": "[{\"label\":\"retinitis pigmentosa\",\"id\":\"DOID:10584\"}]" }, { "gene_id": 320302, "description": "glycosyltransferase 28 domain containing 2", "gene_symbol": "[\"Glt28d2\"]", "do": null }, { "gene_id": 320332, "description": "H4 histone 16", "gene_symbol": "[\"H4c16\"]", "do": null }, { "gene_id": 320343, "description": "LY6/PLAUR domain containing 6", "gene_symbol": "[\"Lypd6\"]", "do": null }, { "gene_id": 320365, "description": "FRY microtubule binding protein", "gene_symbol": "[\"Fry\"]", "do": null }, { "gene_id": 320376, "description": "BCL6 co-repressor-like 1", "gene_symbol": "[\"Bcorl1\"]", "do": null }, { "gene_id": 320398, "description": "leucine-rich repeats and immunoglobulin-like domains 3", "gene_symbol": "[\"Lrig3\"]", "do": null }, { "gene_id": 320405, "description": "Ca2+-dependent activator protein for secretion 2", "gene_symbol": "[\"Cadps2\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 320407, "description": "killer cell lectin-like receptor family I member 2", "gene_symbol": "[\"Klri2\"]", "do": null }, { "gene_id": 320438, "description": "ALG6 alpha-1,3-glucosyltransferase", "gene_symbol": "[\"Alg6\"]", "do": null }, { "gene_id": 320454, "description": "transmembrane protease, serine 11g", "gene_symbol": "[\"Tmprss11g\"]", "do": null }, { "gene_id": 320495, "description": "interaction protein for cytohesin exchange factors 1", "gene_symbol": "[\"Ipcef1\"]", "do": null }, { "gene_id": 320506, "description": "LMBR1 domain containing 2", "gene_symbol": "[\"Lmbrd2\"]", "do": null }, { "gene_id": 320508, "description": "cache domain containing 1", "gene_symbol": "[\"Cachd1\"]", "do": null }, { "gene_id": 320528, "description": "vacuolar protein sorting 13C", "gene_symbol": "[\"Vps13c\"]", "do": null }, { "gene_id": 320534, "description": "solute carrier family 38 member 12", "gene_symbol": "[\"Slc38a12\"]", "do": null }, { "gene_id": 320538, "description": "ubinuclein 2", "gene_symbol": "[\"Ubn2\"]", "do": null }, { "gene_id": 320563, "description": "immunoglobulin superfamily containing leucine-rich repeat 2", "gene_symbol": "[\"Islr2\"]", "do": null }, { "gene_id": 320595, "description": "PHD finger protein 8", "gene_symbol": "[\"Phf8\"]", "do": "[{\"label\":\"syndromic X-linked intellectual disability Siderius type\",\"id\":\"DOID:0060812\"}]" }, { "gene_id": 320604, "description": "coiled-coil domain containing 169", "gene_symbol": "[\"Ccdc169\"]", "do": null }, { "gene_id": 320632, "description": "small nuclear ribonucleoprotein 200 (U5)", "gene_symbol": "[\"Snrnp200\"]", "do": null }, { "gene_id": 320640, "description": "selection and upkeep of intraepithelial T cells 4", "gene_symbol": "[\"Skint4\"]", "do": null }, { "gene_id": 320655, "description": "post-GPI attachment to proteins 3", "gene_symbol": "[\"Pgap3\"]", "do": null }, { "gene_id": 320678, "description": "intermediate filament family orphan 1", "gene_symbol": "[\"Iffo1\"]", "do": null }, { "gene_id": 320685, "description": "dCMP deaminase", "gene_symbol": "[\"Dctd\"]", "do": null }, { "gene_id": 320696, "description": "coiled-coil domain containing 158", "gene_symbol": "[\"Ccdc158\"]", "do": null }, { "gene_id": 320709, "description": "transmembrane protein 117", "gene_symbol": "[\"Tmem117\"]", "do": null }, { "gene_id": 320712, "description": "ABI family member 3 binding protein", "gene_symbol": "[\"Abi3bp\"]", "do": null }, { "gene_id": 320736, "description": "V-set and transmembrane domain containing 4", "gene_symbol": "[\"Vstm4\"]", "do": null }, { "gene_id": 320747, "description": "leucine rich repeat and Ig domain containing 4", "gene_symbol": "[\"Lingo4\"]", "do": null }, { "gene_id": 320752, "description": "dpy-19 like 2", "gene_symbol": "[\"Dpy19l2\"]", "do": null }, { "gene_id": 320769, "description": "peroxiredoxin 6B", "gene_symbol": "[\"Prdx6b\"]", "do": null }, { "gene_id": 320772, "description": "MAM domain containing glycosylphosphatidylinositol anchor 2", "gene_symbol": "[\"Mdga2\"]", "do": null }, { "gene_id": 320795, "description": "protein kinase N1", "gene_symbol": "[\"Pkn1\"]", "do": null }, { "gene_id": 320799, "description": "zinc fingers and homeoboxes 3", "gene_symbol": "[\"Zhx3\"]", "do": null }, { "gene_id": 320840, "description": "neuronal growth regulator 1", "gene_symbol": "[\"Negr1\"]", "do": null }, { "gene_id": 320844, "description": "adhesion molecule with Ig like domain 3", "gene_symbol": "[\"Amigo3\"]", "do": null }, { "gene_id": 320865, "description": "cadherin 18", "gene_symbol": "[\"Cdh18\"]", "do": null }, { "gene_id": 320873, "description": "cadherin 10", "gene_symbol": "[\"Cdh10\"]", "do": null }, { "gene_id": 320910, "description": "integrin beta 8", "gene_symbol": "[\"Itgb8\"]", "do": null }, { "gene_id": 320916, "description": "WSC domain containing 2", "gene_symbol": "[\"Wscd2\"]", "do": null }, { "gene_id": 320924, "description": "collagen and calcium binding EGF domains 1", "gene_symbol": "[\"Ccbe1\"]", "do": null }, { "gene_id": 320974, "description": "leucine rich repeat neuronal 4", "gene_symbol": "[\"Lrrn4\"]", "do": null }, { "gene_id": 320981, "description": "ectonucleotide pyrophosphatase/phosphodiesterase 6", "gene_symbol": "[\"Enpp6\"]", "do": null }, { "gene_id": 321000, "description": "ligand dependent nuclear receptor interacting factor 1", "gene_symbol": "[\"Lrif1\"]", "do": null }, { "gene_id": 321006, "description": "DDB1 and CUL4 associated factor 1", "gene_symbol": "[\"Dcaf1\"]", "do": null }, { "gene_id": 321019, "description": "G protein-coupled receptor 183", "gene_symbol": "[\"Gpr183\"]", "do": null }, { "gene_id": 321020, "description": "formyl peptide receptor, related sequence 6", "gene_symbol": "[\"Fpr-rs6\"]", "do": null }, { "gene_id": 321021, "description": "formyl peptide receptor, related sequence 7", "gene_symbol": "[\"Fpr-rs7\"]", "do": null }, { "gene_id": 321022, "description": "carnitine deficiency-associated gene expressed in ventricle 3", "gene_symbol": "[\"Cdv3\"]", "do": null }, { "gene_id": 326619, "description": "H4 clustered histone 1", "gene_symbol": "[\"H4c1\"]", "do": null }, { "gene_id": 326620, "description": "H4 clustered histone 2", "gene_symbol": "[\"H4c2\"]", "do": null }, { "gene_id": 326623, "description": "tumor necrosis factor (ligand) superfamily, member 15", "gene_symbol": "[\"Tnfsf15\"]", "do": "[{\"label\":\"inflammatory bowel disease 16\",\"id\":\"DOID:0110896\"}]" }, { "gene_id": 327743, "description": "cellular communication network factor 6", "gene_symbol": "[\"Ccn6\"]", "do": "[{\"label\":\"breast metaplastic carcinoma\",\"id\":\"DOID:4680\"},{\"label\":\"progressive pseudorheumatoid arthropathy of childhood\",\"id\":\"DOID:0090004\"}]" }, { "gene_id": 327766, "description": "transmembrane protein 26", "gene_symbol": "[\"Tmem26\"]", "do": null }, { "gene_id": 327799, "description": "ubiquitin specific peptidase 44", "gene_symbol": "[\"Usp44\"]", "do": null }, { "gene_id": 327814, "description": "protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 2", "gene_symbol": "[\"Ppfia2\"]", "do": null }, { "gene_id": 327826, "description": "fibroblast growth factor receptor substrate 2", "gene_symbol": "[\"Frs2\"]", "do": null }, { "gene_id": 328133, "description": "solute carrier family 39 (zinc transporter), member 9", "gene_symbol": "[\"Slc39a9\"]", "do": null }, { "gene_id": 328250, "description": "NUT family member 2", "gene_symbol": "[\"Nutm2\"]", "do": null }, { "gene_id": 328329, "description": "microtubule associated serine/threonine kinase family member 4", "gene_symbol": "[\"Mast4\"]", "do": "[{\"label\":\"Sertoli cell-only syndrome\",\"id\":\"DOID:0050457\"}]" }, { "gene_id": 328401, "description": "ribonuclease, RNase A family, 9 (non-active)", "gene_symbol": "[\"Rnase9\"]", "do": null }, { "gene_id": 328417, "description": "poly (ADP-ribose) polymerase family, member 4", "gene_symbol": "[\"Parp4\"]", "do": null }, { "gene_id": 328505, "description": "selection and upkeep of intraepithelial T cells 7", "gene_symbol": "[\"Skint7\"]", "do": null }, { "gene_id": 328572, "description": "E1A binding protein p300", "gene_symbol": "[\"Ep300\"]", "do": "[{\"label\":\"systemic lupus erythematosus\",\"id\":\"DOID:9074\"}]" }, { "gene_id": 328580, "description": "tubulin, gamma complex component 6", "gene_symbol": "[\"Tubgcp6\"]", "do": null }, { "gene_id": 328779, "description": "heparan sulfate (glucosamine) 3-O-sulfotransferase 6", "gene_symbol": "[\"Hs3st6\"]", "do": null }, { "gene_id": 328780, "description": "serine protease 34", "gene_symbol": "[\"Prss34\"]", "do": null }, { "gene_id": 328783, "description": "mesothelin-like", "gene_symbol": "[\"Mslnl\"]", "do": null }, { "gene_id": 328830, "description": "triggering receptor expressed on myeloid cells 4", "gene_symbol": "[\"Trem4\"]", "do": null }, { "gene_id": 328833, "description": "triggering receptor expressed on myeloid cells-like 2", "gene_symbol": "[\"Treml2\"]", "do": null }, { "gene_id": 328977, "description": "zinc finger protein 532", "gene_symbol": "[\"Zfp532\"]", "do": null }, { "gene_id": 329003, "description": "zinc finger protein 516", "gene_symbol": "[\"Zfp516\"]", "do": null }, { "gene_id": 329015, "description": "autophagy related 2A", "gene_symbol": "[\"Atg2a\"]", "do": null }, { "gene_id": 329064, "description": "polycystic kidney disease 2-like 1", "gene_symbol": "[\"Pkd2l1\"]", "do": null }, { "gene_id": 329093, "description": "carboxypeptidase A6", "gene_symbol": "[\"Cpa6\"]", "do": null }, { "gene_id": 329165, "description": "abl interactor 2", "gene_symbol": "[\"Abi2\"]", "do": null }, { "gene_id": 329178, "description": "unc-80, NALCN activator", "gene_symbol": "[\"Unc80\"]", "do": null }, { "gene_id": 329244, "description": "interleukin 19", "gene_symbol": "[\"Il19\"]", "do": null }, { "gene_id": 329251, "description": "protein phosphatase 1, regulatory subunit 12B", "gene_symbol": "[\"Ppp1r12b\"]", "do": null }, { "gene_id": 329252, "description": "leucine-rich repeat-containing G protein-coupled receptor 6", "gene_symbol": "[\"Lgr6\"]", "do": null }, { "gene_id": 329278, "description": "tenascin N", "gene_symbol": "[\"Tnn\"]", "do": null }, { "gene_id": 329547, "description": "bactericidal permeablility increasing protein", "gene_symbol": "[\"Bpi\"]", "do": null }, { "gene_id": 329559, "description": "zinc finger protein 335", "gene_symbol": "[\"Zfp335\"]", "do": null }, { "gene_id": 329628, "description": "FAT atypical cadherin 4", "gene_symbol": "[\"Fat4\"]", "do": null }, { "gene_id": 329659, "description": "mitochondrial inner membrane subdomain organizer 1", "gene_symbol": "[\"Miso1\"]", "do": null }, { "gene_id": 329693, "description": "Fc receptor-like 5", "gene_symbol": "[\"Fcrl5\"]", "do": null }, { "gene_id": 329702, "description": "DC-STAMP domain containing 2", "gene_symbol": "[\"Dcst2\"]", "do": null }, { "gene_id": 329777, "description": "phosphatidylinositol glycan anchor biosynthesis, class K", "gene_symbol": "[\"Pigk\"]", "do": null }, { "gene_id": 329795, "description": "transmembrane protein 67", "gene_symbol": "[\"Tmem67\"]", "do": "[{\"label\":\"Joubert syndrome 6\",\"id\":\"DOID:0111001\"},{\"label\":\"Meckel syndrome\",\"id\":\"DOID:0050778\"},{\"label\":\"cystic kidney disease\",\"id\":\"DOID:2975\"},{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 329828, "description": "myogenesis regulating glycosidase (putative)", "gene_symbol": "[\"Myorg\"]", "do": "[{\"label\":\"basal ganglia calcification\",\"id\":\"DOID:0060230\"}]" }, { "gene_id": 329872, "description": "Fras1 related extracellular matrix protein 1", "gene_symbol": "[\"Frem1\"]", "do": "[{\"label\":\"Fraser syndrome\",\"id\":\"DOID:0090001\"},{\"label\":\"chromosome 9p deletion syndrome\",\"id\":\"DOID:0060732\"},{\"label\":\"congenital diaphragmatic hernia\",\"id\":\"DOID:3827\"}]" }, { "gene_id": 329908, "description": "ubiquitin specific peptidase 24", "gene_symbol": "[\"Usp24\"]", "do": null }, { "gene_id": 329918, "description": "selection and upkeep of intraepithelial T cells 9", "gene_symbol": "[\"Skint9\"]", "do": null }, { "gene_id": 329919, "description": "selection and upkeep of intraepithelial T cells 2", "gene_symbol": "[\"Skint2\"]", "do": null }, { "gene_id": 329941, "description": "collagen, type VIII, alpha 2", "gene_symbol": "[\"Col8a2\"]", "do": "[{\"label\":\"Fuchs' endothelial dystrophy\",\"id\":\"DOID:11555\"}]" }, { "gene_id": 330064, "description": "solute carrier family 5 (sodium-dependent vitamin transporter), member 6", "gene_symbol": "[\"Slc5a6\"]", "do": null }, { "gene_id": 330217, "description": "galactose-3-O-sulfotransferase 4", "gene_symbol": "[\"Gal3st4\"]", "do": null }, { "gene_id": 330222, "description": "sidekick cell adhesion molecule 1", "gene_symbol": "[\"Sdk1\"]", "do": null }, { "gene_id": 330260, "description": "paraoxonase 2", "gene_symbol": "[\"Pon2\"]", "do": null }, { "gene_id": 330267, "description": "thrombospondin, type I, domain containing 7A", "gene_symbol": "[\"Thsd7a\"]", "do": null }, { "gene_id": 330286, "description": "RIKEN cDNA D630045J12 gene", "gene_symbol": "[\"D630045J12Rik\"]", "do": null }, { "gene_id": 330323, "description": "MINDY lysine 48 deubiquitinase 4", "gene_symbol": "[\"Mindy4\"]", "do": null }, { "gene_id": 330369, "description": "F-box protein 41", "gene_symbol": "[\"Fbxo41\"]", "do": null }, { "gene_id": 330406, "description": "beta-1,4-N-acetyl-galactosaminyl transferase 3", "gene_symbol": "[\"B4galnt3\"]", "do": null }, { "gene_id": 330460, "description": "transmembrane protein 150B", "gene_symbol": "[\"Tmem150b\"]", "do": null }, { "gene_id": 330470, "description": "binder of sperm protein homolog 1", "gene_symbol": "[\"Bsph1\"]", "do": null }, { "gene_id": 330483, "description": "CEA cell adhesion molecule 16", "gene_symbol": "[\"Ceacam16\"]", "do": "[{\"label\":\"autosomal dominant nonsyndromic deafness 4A\",\"id\":\"DOID:0110573\"}]" }, { "gene_id": 330485, "description": "transmembrane protein 145", "gene_symbol": "[\"Tmem145\"]", "do": null }, { "gene_id": 330496, "description": "interferon lambda 2", "gene_symbol": "[\"Ifnl2\"]", "do": null }, { "gene_id": 330671, "description": "beta-1,4-N-acetyl-galactosaminyl transferase 4", "gene_symbol": "[\"B4galnt4\"]", "do": null }, { "gene_id": 330790, "description": "hyaluronan and proteoglycan link protein 4", "gene_symbol": "[\"Hapln4\"]", "do": null }, { "gene_id": 330812, "description": "ring finger protein 150", "gene_symbol": "[\"Rnf150\"]", "do": null }, { "gene_id": 330814, "description": "adhesion G protein-coupled receptor L1", "gene_symbol": "[\"Adgrl1\"]", "do": null }, { "gene_id": 330863, "description": "tripartite motif-containing 67", "gene_symbol": "[\"Trim67\"]", "do": null }, { "gene_id": 330908, "description": "opioid binding protein/cell adhesion molecule-like", "gene_symbol": "[\"Opcml\"]", "do": null }, { "gene_id": 330914, "description": "Rho GTPase activating protein 32", "gene_symbol": "[\"Arhgap32\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 330941, "description": "expressed sequence AI593442", "gene_symbol": "[\"AI593442\"]", "do": null }, { "gene_id": 330953, "description": "hyperpolarization-activated, cyclic nucleotide-gated K+ 4", "gene_symbol": "[\"Hcn4\"]", "do": null }, { "gene_id": 331004, "description": "solute carrier family 9 (sodium/hydrogen exchanger), member 9", "gene_symbol": "[\"Slc9a9\"]", "do": "[{\"label\":\"autism spectrum disorder\",\"id\":\"DOID:0060041\"}]" }, { "gene_id": 331046, "description": "transglutaminase 4 (prostate)", "gene_symbol": "[\"Tgm4\"]", "do": null }, { "gene_id": 331401, "description": "THO complex 2", "gene_symbol": "[\"Thoc2\"]", "do": "[{\"label\":\"X-linked intellectual disability-short stature-overweight syndrome\",\"id\":\"DOID:0112056\"}]" }, { "gene_id": 331461, "description": "interleukin 1 receptor accessory protein-like 1", "gene_symbol": "[\"Il1rapl1\"]", "do": null }, { "gene_id": 331532, "description": "transcription elongation factor A (SII)-like 5", "gene_symbol": "[\"Tceal5\"]", "do": null }, { "gene_id": 331535, "description": "serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 7", "gene_symbol": "[\"Serpina7\"]", "do": null }, { "gene_id": 332396, "description": "potassium channel, subfamily K, member 18", "gene_symbol": "[\"Kcnk18\"]", "do": null }, { "gene_id": 332427, "description": "lysozyme G-like 2", "gene_symbol": "[\"Lyg2\"]", "do": null }, { "gene_id": 332578, "description": "lipocalin 10", "gene_symbol": "[\"Lcn10\"]", "do": null }, { "gene_id": 333050, "description": "kinase suppressor of ras 2", "gene_symbol": "[\"Ksr2\"]", "do": null }, { "gene_id": 333088, "description": "kielin/chordin-like protein", "gene_symbol": "[\"Kcp\"]", "do": null }, { "gene_id": 333424, "description": "alpha-1,4-N-acetylglucosaminyltransferase", "gene_symbol": "[\"A4gnt\"]", "do": null }, { "gene_id": 333433, "description": "glycerol-3-phosphate dehydrogenase 1-like", "gene_symbol": "[\"Gpd1l\"]", "do": null }, { "gene_id": 333639, "description": "mastermind-like domain containing 1", "gene_symbol": "[\"Mamld1\"]", "do": null }, { "gene_id": 333669, "description": "predicted gene 5134", "gene_symbol": "[\"Gm5134\"]", "do": null }, { "gene_id": 333883, "description": "CD59b antigen", "gene_symbol": "[\"Cd59b\"]", "do": null }, { "gene_id": 338320, "description": "MIA SH3 domain ER export factor 2", "gene_symbol": "[\"Mia2\"]", "do": null }, { "gene_id": 338346, "description": "G protein-coupled receptor 21", "gene_symbol": "[\"Gpr21\"]", "do": null }, { "gene_id": 338352, "description": "NEL-like 1", "gene_symbol": "[\"Nell1\"]", "do": null }, { "gene_id": 338355, "description": "FK506 binding protein 15", "gene_symbol": "[\"Fkbp15\"]", "do": null }, { "gene_id": 338362, "description": "uronyl-2-sulfotransferase", "gene_symbol": "[\"Ust\"]", "do": null }, { "gene_id": 338366, "description": "MIA SH3 domain ER export factor 3", "gene_symbol": "[\"Mia3\"]", "do": null }, { "gene_id": 338367, "description": "myosin ID", "gene_symbol": "[\"Myo1d\"]", "do": null }, { "gene_id": 338370, "description": "sodium leak channel, non-selective", "gene_symbol": "[\"Nalcn\"]", "do": null }, { "gene_id": 338467, "description": "microrchidia 3", "gene_symbol": "[\"Morc3\"]", "do": null }, { "gene_id": 353148, "description": "taste receptor, type 2, member 139", "gene_symbol": "[\"Tas2r139\"]", "do": null }, { "gene_id": 353166, "description": "taste receptor, type 2, member 117", "gene_symbol": "[\"Tas2r117\"]", "do": null }, { "gene_id": 353167, "description": "taste receptor, type 2, member 123", "gene_symbol": "[\"Tas2r123\"]", "do": null }, { "gene_id": 353169, "description": "solute carrier family 2 (facilitated glucose transporter), member 12", "gene_symbol": "[\"Slc2a12\"]", "do": null }, { "gene_id": 353188, "description": "a disintegrin and metallopeptidase domain 32", "gene_symbol": "[\"Adam32\"]", "do": null }, { "gene_id": 353237, "description": "protocadherin alpha subfamily C, 2", "gene_symbol": "[\"Pcdhac2\"]", "do": null }, { "gene_id": 353310, "description": "zinc finger protein 703", "gene_symbol": "[\"Zfp703\"]", "do": null }, { "gene_id": 353328, "description": "mucin 6, gastric", "gene_symbol": "[\"Muc6\"]", "do": null }, { "gene_id": 353344, "description": "opsin 5", "gene_symbol": "[\"Opn5\"]", "do": null }, { "gene_id": 353346, "description": "G protein-coupled receptor 141", "gene_symbol": "[\"Gpr141\"]", "do": null }, { "gene_id": 353499, "description": "transmembrane channel-like gene family 4", "gene_symbol": "[\"Tmc4\"]", "do": null }, { "gene_id": 360013, "description": "myosin XVIIIA", "gene_symbol": "[\"Myo18a\"]", "do": null }, { "gene_id": 368202, "description": "serine protease 48", "gene_symbol": "[\"Prss48\"]", "do": null }, { "gene_id": 373864, "description": "collagen, type XXVII, alpha 1", "gene_symbol": "[\"Col27a1\"]", "do": null }, { "gene_id": 378431, "description": "taxilin beta", "gene_symbol": "[\"Txlnb\"]", "do": null }, { "gene_id": 378700, "description": "BPI fold containing family B, member 3", "gene_symbol": "[\"Bpifb3\"]", "do": null }, { "gene_id": 378702, "description": "small EDRK-rich factor 2", "gene_symbol": "[\"Serf2\"]", "do": null }, { "gene_id": 378937, "description": "leucine rich repeat containing 24", "gene_symbol": "[\"Lrrc24\"]", "do": null }, { "gene_id": 379043, "description": "retinoic acid early transcript 1E", "gene_symbol": "[\"Raet1e\"]", "do": null }, { "gene_id": 380608, "description": "T cell activation GTPase activating protein 1", "gene_symbol": "[\"Tagap1\"]", "do": null }, { "gene_id": 380664, "description": "LEM domain containing 3", "gene_symbol": "[\"Lemd3\"]", "do": null }, { "gene_id": 380684, "description": "neurofilament, heavy polypeptide", "gene_symbol": "[\"Nefh\"]", "do": null }, { "gene_id": 380702, "description": "shisa family member 6", "gene_symbol": "[\"Shisa6\"]", "do": null }, { "gene_id": 380711, "description": "RAP1 GTPase activating protein 2", "gene_symbol": "[\"Rap1gap2\"]", "do": null }, { "gene_id": 380713, "description": "scavenger receptor class F, member 1", "gene_symbol": "[\"Scarf1\"]", "do": null }, { "gene_id": 380730, "description": "leucine rich repeat containing 37", "gene_symbol": "[\"Lrrc37\"]", "do": null }, { "gene_id": 380732, "description": "mast cell immunoglobulin like receptor 1", "gene_symbol": "[\"Milr1\"]", "do": null }, { "gene_id": 380780, "description": "serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 11", "gene_symbol": "[\"Serpina11\"]", "do": null }, { "gene_id": 380785, "description": "brain-enriched guanylate kinase-associated", "gene_symbol": "[\"Begain\"]", "do": null }, { "gene_id": 380921, "description": "diacylglycerol kinase, eta", "gene_symbol": "[\"Dgkh\"]", "do": null }, { "gene_id": 380924, "description": "olfactomedin 4", "gene_symbol": "[\"Olfm4\"]", "do": null }, { "gene_id": 380959, "description": "ALG10 alpha-1,2-glucosyltransferase", "gene_symbol": "[\"Alg10\"]", "do": "[{\"label\":\"nonsyndromic deafness\",\"id\":\"DOID:0050563\"}]" }, { "gene_id": 380967, "description": "transmembrane protein 106C", "gene_symbol": "[\"Tmem106c\"]", "do": null }, { "gene_id": 380969, "description": "NCK-associated protein 5-like", "gene_symbol": "[\"Nckap5l\"]", "do": null }, { "gene_id": 381058, "description": "unc-93 homolog A", "gene_symbol": "[\"Unc93a\"]", "do": null }, { "gene_id": 381072, "description": "ATP-binding cassette, sub-family A member 17", "gene_symbol": "[\"Abca17\"]", "do": null }, { "gene_id": 381101, "description": "2'-deoxynucleoside 5'-phosphate N-hydrolase 1", "gene_symbol": "[\"Dnph1\"]", "do": null }, { "gene_id": 381203, "description": "solute carrier family 22 (organic anion transporter), member 20", "gene_symbol": "[\"Slc22a20\"]", "do": null }, { "gene_id": 381204, "description": "N-acetylated alpha-linked acidic dipeptidase-like 1", "gene_symbol": "[\"Naaladl1\"]", "do": null }, { "gene_id": 381236, "description": "lipase, member O3", "gene_symbol": "[\"Lipo3\"]", "do": null }, { "gene_id": 381284, "description": "ciliary rootlet coiled-coil, rootletin family member 2", "gene_symbol": "[\"Crocc2\"]", "do": null }, { "gene_id": 381290, "description": "ATPase, Ca++ transporting, plasma membrane 4", "gene_symbol": "[\"Atp2b4\"]", "do": null }, { "gene_id": 381314, "description": "isoleucine-tRNA synthetase 2, mitochondrial", "gene_symbol": "[\"Iars2\"]", "do": null }, { "gene_id": 381334, "description": "galactose-3-O-sulfotransferase 2", "gene_symbol": "[\"Gal3st2\"]", "do": null }, { "gene_id": 381339, "description": "transmembrane protein 182", "gene_symbol": "[\"Tmem182\"]", "do": null }, { "gene_id": 381353, "description": "apical junction component 1", "gene_symbol": "[\"Ajm1\"]", "do": null }, { "gene_id": 381399, "description": "BPI fold containing family B, member 4", "gene_symbol": "[\"Bpifb4\"]", "do": null }, { "gene_id": 381409, "description": "cadherin-like 26", "gene_symbol": "[\"Cdh26\"]", "do": null }, { "gene_id": 381413, "description": "G protein-coupled receptor 176", "gene_symbol": "[\"Gpr176\"]", "do": null }, { "gene_id": 381417, "description": "solute carrier family 28 member 2b", "gene_symbol": "[\"Slc28a2b\"]", "do": null }, { "gene_id": 381489, "description": "relaxin/insulin-like family peptide receptor 1", "gene_symbol": "[\"Rxfp1\"]", "do": null }, { "gene_id": 381510, "description": "dpy-19 like 4", "gene_symbol": "[\"Dpy19l4\"]", "do": null }, { "gene_id": 381531, "description": "major urinary protein 21", "gene_symbol": "[\"Mup21\"]", "do": null }, { "gene_id": 381538, "description": "maestro heat-like repeat family member 7", "gene_symbol": "[\"Mroh7\"]", "do": null }, { "gene_id": 381569, "description": "PRAME like 26", "gene_symbol": "[\"Pramel26\"]", "do": null }, { "gene_id": 381570, "description": "oogenesin 2", "gene_symbol": "[\"Oog2\"]", "do": null }, { "gene_id": 381572, "description": "AADACL4 family member 1", "gene_symbol": "[\"Aadacl4fm1\"]", "do": null }, { "gene_id": 381605, "description": "TBC1 domain family, member 2", "gene_symbol": "[\"Tbc1d2\"]", "do": null }, { "gene_id": 381626, "description": "RNA binding motif protein 33", "gene_symbol": "[\"Rbm33\"]", "do": null }, { "gene_id": 381628, "description": "adhesion G protein-coupled receptor F3", "gene_symbol": "[\"Adgrf3\"]", "do": null }, { "gene_id": 381629, "description": "all-trans retinoic acid induced differentiation factor", "gene_symbol": "[\"Atraid\"]", "do": null }, { "gene_id": 381694, "description": "beta-3-glucosyltransferase", "gene_symbol": "[\"B3glct\"]", "do": "[{\"label\":\"Peters plus syndrome\",\"id\":\"DOID:0080201\"}]" }, { "gene_id": 381716, "description": "PTTG1IP family member 2", "gene_symbol": "[\"Pttg1ip2\"]", "do": null }, { "gene_id": 381738, "description": "dynein regulatory complex subunit 1", "gene_symbol": "[\"Drc1\"]", "do": "[{\"label\":\"Kartagener syndrome\",\"id\":\"DOID:0050144\"},{\"label\":\"primary ciliary dyskinesia 21\",\"id\":\"DOID:0110596\"},{\"label\":\"visceral heterotaxy\",\"id\":\"DOID:0050545\"}]" }, { "gene_id": 381810, "description": "lysophosphatidic acid receptor 5", "gene_symbol": "[\"Lpar5\"]", "do": null }, { "gene_id": 381853, "description": "gastric inhibitory polypeptide receptor", "gene_symbol": "[\"Gipr\"]", "do": null }, { "gene_id": 381903, "description": "ALG8 alpha-1,3-glucosyltransferase", "gene_symbol": "[\"Alg8\"]", "do": null }, { "gene_id": 381924, "description": "integrin, alpha D", "gene_symbol": "[\"Itgad\"]", "do": null }, { "gene_id": 381983, "description": "lemur tyrosine kinase 3", "gene_symbol": "[\"Lmtk3\"]", "do": null }, { "gene_id": 382014, "description": "anoctamin 8", "gene_symbol": "[\"Ano8\"]", "do": null }, { "gene_id": 382018, "description": "unc-13 homolog A", "gene_symbol": "[\"Unc13a\"]", "do": null }, { "gene_id": 382034, "description": "genetic suppressor element 1, coiled-coil protein", "gene_symbol": "[\"Gse1\"]", "do": null }, { "gene_id": 382035, "description": "poly(A)binding protein nuclear 1-like", "gene_symbol": "[\"Pabpn1l\"]", "do": null }, { "gene_id": 382045, "description": "adhesion G protein-coupled receptor G5", "gene_symbol": "[\"Adgrg5\"]", "do": null }, { "gene_id": 382053, "description": "carboxylesterase 3A", "gene_symbol": "[\"Ces3a\"]", "do": null }, { "gene_id": 382056, "description": "CREB regulated transcription coactivator 1", "gene_symbol": "[\"Crtc1\"]", "do": "[{\"label\":\"major depressive disorder\",\"id\":\"DOID:1470\"}]" }, { "gene_id": 382097, "description": "predicted gene 1123", "gene_symbol": "[\"Gm1123\"]", "do": null }, { "gene_id": 382113, "description": "solute carrier family 22 (organic cation transporter), member 14", "gene_symbol": "[\"Slc22a14\"]", "do": null }, { "gene_id": 382117, "description": "T cell activation inhibitor, mitochondrial", "gene_symbol": "[\"Tcaim\"]", "do": null }, { "gene_id": 382118, "description": "zinc finger with KRAB and SCAN domains 7", "gene_symbol": "[\"Zkscan7\"]", "do": null }, { "gene_id": 382236, "description": "bromodomain and WD repeat domain containing 3", "gene_symbol": "[\"Brwd3\"]", "do": null }, { "gene_id": 382253, "description": "cyclin dependent kinase like 5", "gene_symbol": "[\"Cdkl5\"]", "do": "[{\"label\":\"developmental and epileptic encephalopathy 2\",\"id\":\"DOID:0080467\"}]" }, { "gene_id": 382348, "description": "trace amine-associated receptor 8B", "gene_symbol": "[\"Taar8b\"]", "do": null }, { "gene_id": 382423, "description": "ataxin 7-like 3B", "gene_symbol": "[\"Atxn7l3b\"]", "do": null }, { "gene_id": 382522, "description": "H2B clustered histone 26", "gene_symbol": "[\"H2bc26\"]", "do": null }, { "gene_id": 382913, "description": "nei like 2 (E. coli)", "gene_symbol": "[\"Neil2\"]", "do": null }, { "gene_id": 383348, "description": "potassium channel tetramerisation domain containing 16", "gene_symbol": "[\"Kctd16\"]", "do": null }, { "gene_id": 383491, "description": "PR domain containing 14", "gene_symbol": "[\"Prdm14\"]", "do": null }, { "gene_id": 384059, "description": "toll-like receptor 12", "gene_symbol": "[\"Tlr12\"]", "do": null }, { "gene_id": 384061, "description": "fibronectin type III domain containing 5", "gene_symbol": "[\"Fndc5\"]", "do": null }, { "gene_id": 384783, "description": "insulin receptor substrate 2", "gene_symbol": "[\"Irs2\"]", "do": "[{\"label\":\"type 2 diabetes mellitus\",\"id\":\"DOID:9352\"}]" }, { "gene_id": 384997, "description": "peptidoglycan recognition protein 4", "gene_symbol": "[\"Pglyrp4\"]", "do": null }, { "gene_id": 385643, "description": "kininogen 2", "gene_symbol": "[\"Kng2\"]", "do": null }, { "gene_id": 386611, "description": "ring finger protein 133", "gene_symbol": "[\"Rnf133\"]", "do": null }, { "gene_id": 386750, "description": "SLIT and NTRK-like family, member 3", "gene_symbol": "[\"Slitrk3\"]", "do": null }, { "gene_id": 387285, "description": "hypocretin (orexin) receptor 2", "gene_symbol": "[\"Hcrtr2\"]", "do": "[{\"label\":\"narcolepsy\",\"id\":\"DOID:8986\"}]" }, { "gene_id": 387314, "description": "transmembrane and tetratricopeptide repeat containing 1", "gene_symbol": "[\"Tmtc1\"]", "do": null }, { "gene_id": 387340, "description": "taste receptor, type 2, member 104", "gene_symbol": "[\"Tas2r104\"]", "do": null }, { "gene_id": 387341, "description": "taste receptor, type 2, member 106", "gene_symbol": "[\"Tas2r106\"]", "do": null }, { "gene_id": 387342, "description": "taste receptor, type 2, member 107", "gene_symbol": "[\"Tas2r107\"]", "do": null }, { "gene_id": 387343, "description": "taste receptor, type 2, member 109", "gene_symbol": "[\"Tas2r109\"]", "do": null }, { "gene_id": 387344, "description": "taste receptor, type 2, member 110", "gene_symbol": "[\"Tas2r110\"]", "do": null }, { "gene_id": 387345, "description": "taste receptor, type 2, member 113", "gene_symbol": "[\"Tas2r113\"]", "do": null }, { "gene_id": 387346, "description": "taste receptor, type 2, member 114", "gene_symbol": "[\"Tas2r114\"]", "do": null }, { "gene_id": 387347, "description": "taste receptor, type 2, member 118", "gene_symbol": "[\"Tas2r118\"]", "do": null }, { "gene_id": 387348, "description": "taste receptor, type 2, member 120", "gene_symbol": "[\"Tas2r120\"]", "do": null }, { "gene_id": 387349, "description": "taste receptor, type 2, member 121", "gene_symbol": "[\"Tas2r121\"]", "do": null }, { "gene_id": 387351, "description": "taste receptor, type 2, member 124", "gene_symbol": "[\"Tas2r124\"]", "do": null }, { "gene_id": 387352, "description": "taste receptor, type 2, member 125", "gene_symbol": "[\"Tas2r125\"]", "do": null }, { "gene_id": 387353, "description": "taste receptor, type 2, member 126", "gene_symbol": "[\"Tas2r126\"]", "do": null }, { "gene_id": 387354, "description": "taste receptor, type 2, member 129", "gene_symbol": "[\"Tas2r129\"]", "do": null }, { "gene_id": 387355, "description": "taste receptor, type 2, member 130", "gene_symbol": "[\"Tas2r130\"]", "do": null }, { "gene_id": 387511, "description": "taste receptor, type 2, member 134", "gene_symbol": "[\"Tas2r134\"]", "do": null }, { "gene_id": 387512, "description": "taste receptor, type 2, member 135", "gene_symbol": "[\"Tas2r135\"]", "do": null }, { "gene_id": 387513, "description": "taste receptor, type 2, member 138", "gene_symbol": "[\"Tas2r138\"]", "do": null }, { "gene_id": 387514, "description": "taste receptor, type 2, member 143", "gene_symbol": "[\"Tas2r143\"]", "do": null }, { "gene_id": 387515, "description": "taste receptor, type 2, member 144", "gene_symbol": "[\"Tas2r144\"]", "do": null }, { "gene_id": 387609, "description": "zinc fingers and homeoboxes 2", "gene_symbol": "[\"Zhx2\"]", "do": null }, { "gene_id": 387616, "description": "taste receptor, type 2, member 140", "gene_symbol": "[\"Tas2r140\"]", "do": null }, { "gene_id": 394430, "description": "UDP glycosyltransferase 1 family, polypeptide A10", "gene_symbol": "[\"Ugt1a10\"]", "do": null }, { "gene_id": 394432, "description": "UDP glucuronosyltransferase 1 family, polypeptide A7C", "gene_symbol": "[\"Ugt1a7c\"]", "do": null }, { "gene_id": 394433, "description": "UDP glucuronosyltransferase 1 family, polypeptide A5", "gene_symbol": "[\"Ugt1a5\"]", "do": null }, { "gene_id": 394434, "description": "UDP glucuronosyltransferase 1 family, polypeptide A9", "gene_symbol": "[\"Ugt1a9\"]", "do": null }, { "gene_id": 394435, "description": "UDP glucuronosyltransferase 1 family, polypeptide A6B", "gene_symbol": "[\"Ugt1a6b\"]", "do": null }, { "gene_id": 394436, "description": "UDP glucuronosyltransferase 1 family, polypeptide A1", "gene_symbol": "[\"Ugt1a1\"]", "do": null }, { "gene_id": 396184, "description": "fibronectin leucine rich transmembrane protein 1", "gene_symbol": "[\"Flrt1\"]", "do": null }, { "gene_id": 399548, "description": "sodium channel, type IV, beta", "gene_symbol": "[\"Scn4b\"]", "do": null }, { "gene_id": 399558, "description": "fibronectin leucine rich transmembrane protein 2", "gene_symbol": "[\"Flrt2\"]", "do": null }, { "gene_id": 404194, "description": "GDNF family receptor alpha like", "gene_symbol": "[\"Gfral\"]", "do": null }, { "gene_id": 404237, "description": "MAS-related GPR, member A8", "gene_symbol": "[\"Mrgpra8\"]", "do": null }, { "gene_id": 404239, "description": "MAS-related GPR, member B5", "gene_symbol": "[\"Mrgprb5\"]", "do": null }, { "gene_id": 404240, "description": "MAS-related GPR, member B8", "gene_symbol": "[\"Mrgprb8\"]", "do": null }, { "gene_id": 404242, "description": "MAS-related GPR, member X1", "gene_symbol": "[\"Mrgprx1\"]", "do": null }, { "gene_id": 404545, "description": "anoctamin 7", "gene_symbol": "[\"Ano7\"]", "do": null }, { "gene_id": 404710, "description": "IQ motif containing GTPase activating protein 3", "gene_symbol": "[\"Iqgap3\"]", "do": null }, { "gene_id": 406186, "description": "olfactory receptor family 4 subfamily B member 13", "gene_symbol": "[\"Or4b13\"]", "do": null }, { "gene_id": 406218, "description": "pannexin 2", "gene_symbol": "[\"Panx2\"]", "do": null }, { "gene_id": 406220, "description": "keratin 77", "gene_symbol": "[\"Krt77\"]", "do": null }, { "gene_id": 407786, "description": "TATA-box binding protein associated factor 9B", "gene_symbol": "[\"Taf9b\"]", "do": null }, { "gene_id": 407795, "description": "small integral membrane protein 31", "gene_symbol": "[\"Smim31\"]", "do": null }, { "gene_id": 407800, "description": "extracellular matrix protein 2, female organ and adipocyte specific", "gene_symbol": "[\"Ecm2\"]", "do": null }, { "gene_id": 407831, "description": "transmembrane protein 204", "gene_symbol": "[\"Tmem204\"]", "do": null }, { "gene_id": 414801, "description": "inositol 1,4,5-triphosphate receptor interacting protein", "gene_symbol": "[\"Itprip\"]", "do": null }, { "gene_id": 432442, "description": "A kinase anchor protein 7", "gene_symbol": "[\"Akap7\"]", "do": null }, { "gene_id": 432486, "description": "N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits", "gene_symbol": "[\"Gnptab\"]", "do": "[{\"label\":\"mucolipidosis II alpha/beta\",\"id\":\"DOID:0080070\"}]" }, { "gene_id": 432508, "description": "cleavage and polyadenylation specific factor 6", "gene_symbol": "[\"Cpsf6\"]", "do": null }, { "gene_id": 432516, "description": "myosin IA", "gene_symbol": "[\"Myo1a\"]", "do": null }, { "gene_id": 432530, "description": "adenylate cyclase 1", "gene_symbol": "[\"Adcy1\"]", "do": null }, { "gene_id": 432677, "description": "vertebrae development associated", "gene_symbol": "[\"Vrtn\"]", "do": null }, { "gene_id": 433102, "description": "surfactant associated 2", "gene_symbol": "[\"Sfta2\"]", "do": null }, { "gene_id": 433181, "description": "serine peptidase inhibitor, Kazal type 11", "gene_symbol": "[\"Spink11\"]", "do": null }, { "gene_id": 433182, "description": "enolase 1B, retrotransposed", "gene_symbol": "[\"Eno1b\"]", "do": null }, { "gene_id": 433256, "description": "acyl-CoA synthetase long-chain family member 5", "gene_symbol": "[\"Acsl5\"]", "do": null }, { "gene_id": 433375, "description": "cellular repressor of E1A-stimulated genes 1", "gene_symbol": "[\"Creg1\"]", "do": null }, { "gene_id": 433492, "description": "BPI fold containing family B, member 9B", "gene_symbol": "[\"Bpifb9b\"]", "do": null }, { "gene_id": 433586, "description": "mastermind like transcriptional coactivator 3", "gene_symbol": "[\"Maml3\"]", "do": null }, { "gene_id": 433759, "description": "histone deacetylase 1", "gene_symbol": "[\"Hdac1\"]", "do": null }, { "gene_id": 433926, "description": "leucine rich repeat containing 8 family, member B", "gene_symbol": "[\"Lrrc8b\"]", "do": null }, { "gene_id": 433931, "description": "phosphatidylinositol glycan anchor biosynthesis, class G", "gene_symbol": "[\"Pigg\"]", "do": null }, { "gene_id": 434203, "description": "solute carrier family 28 (sodium-coupled nucleoside transporter), member 1", "gene_symbol": "[\"Slc28a1\"]", "do": null }, { "gene_id": 434215, "description": "leucine rich repeat containing 32", "gene_symbol": "[\"Lrrc32\"]", "do": null }, { "gene_id": 434341, "description": "NLR family, CARD domain containing 5", "gene_symbol": "[\"Nlrc5\"]", "do": null }, { "gene_id": 434674, "description": "solute carrier family 22, member 28", "gene_symbol": "[\"Slc22a28\"]", "do": null }, { "gene_id": 435145, "description": "shisa family member 8", "gene_symbol": "[\"Shisa8\"]", "do": null }, { "gene_id": 435206, "description": "trace amine-associated receptor 7D", "gene_symbol": "[\"Taar7d\"]", "do": null }, { "gene_id": 435207, "description": "trace amine-associated receptor 7F", "gene_symbol": "[\"Taar7f\"]", "do": null }, { "gene_id": 435529, "description": "adhesion G protein-coupled receptor F2", "gene_symbol": "[\"Adgrf2\"]", "do": null }, { "gene_id": 435653, "description": "Fc receptor-like B", "gene_symbol": "[\"Fcrlb\"]", "do": null }, { "gene_id": 435845, "description": "transmembrane protease, serine 11c", "gene_symbol": "[\"Tmprss11c\"]", "do": null }, { "gene_id": 435965, "description": "low density lipoprotein receptor-related protein 3", "gene_symbol": "[\"Lrp3\"]", "do": null }, { "gene_id": 436090, "description": "G protein-coupled receptor 62", "gene_symbol": "[\"Gpr62\"]", "do": null }, { "gene_id": 436440, "description": "G protein-coupled receptor 31, D17Leh66b region", "gene_symbol": "[\"Gpr31b\"]", "do": null }, { "gene_id": 448987, "description": "F-box and leucine-rich repeat protein 7", "gene_symbol": "[\"Fbxl7\"]", "do": null }, { "gene_id": 493583, "description": "intelectin b", "gene_symbol": "[\"Itlnb\"]", "do": null }, { "gene_id": 493809, "description": "trace amine-associated receptor 3", "gene_symbol": "[\"Taar3\"]", "do": null }, { "gene_id": 494468, "description": "armadillo repeat containing, X-linked 5", "gene_symbol": "[\"Armcx5\"]", "do": null }, { "gene_id": 494504, "description": "adenomatosis polyposis coli down-regulated 1", "gene_symbol": "[\"Apcdd1\"]", "do": null }, { "gene_id": 494519, "description": "secretoglobin, family 2B, member 20", "gene_symbol": "[\"Scgb2b20\"]", "do": null }, { "gene_id": 494546, "description": "trace amine-associated receptor 8C", "gene_symbol": "[\"Taar8c\"]", "do": null }, { "gene_id": 497113, "description": "ribonuclease, RNase A family, 11 (non-active)", "gene_symbol": "[\"Rnase11\"]", "do": null }, { "gene_id": 503550, 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"otogelin-like", "gene_symbol": "[\"Otogl\"]", "do": null }, { "gene_id": 630146, "description": "CD101 antigen", "gene_symbol": "[\"Cd101\"]", "do": null }, { "gene_id": 631784, "description": "predicted gene 7073", "gene_symbol": "[\"Gm7073\"]", "do": null }, { "gene_id": 632126, "description": "butyrophilin-like 4", "gene_symbol": "[\"Btnl4\"]", "do": null }, { "gene_id": 634825, "description": "defensin, alpha, 38", "gene_symbol": "[\"Defa38\"]", "do": null }, { "gene_id": 635702, "description": "N-acetylated alpha-linked acidic dipeptidase-like 2", "gene_symbol": "[\"Naaladl2\"]", "do": null }, { "gene_id": 636808, "description": "contactin associated protein-like 5A", "gene_symbol": "[\"Cntnap5a\"]", "do": null }, { "gene_id": 636931, "description": "tripartite motif-containing 71", "gene_symbol": "[\"Trim71\"]", "do": "[{\"label\":\"hydrocephalus\",\"id\":\"DOID:10908\"}]" }, { "gene_id": 639774, "description": "selection and upkeep of intraepithelial T cells 8", "gene_symbol": 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"description": "phospholipase B1", "gene_symbol": "[\"Plb1\"]", "do": null }, { "gene_id": 665775, "description": "biorientation of chromosomes in cell division 1-like", "gene_symbol": "[\"Bod1l\"]", "do": null }, { "gene_id": 666048, "description": "TraB domain containing 2B", "gene_symbol": "[\"Trabd2b\"]", "do": null }, { "gene_id": 666060, "description": "FERM and PDZ domain containing 1", "gene_symbol": "[\"Frmpd1\"]", "do": null }, { "gene_id": 666279, "description": "dentin sialophosphoprotein", "gene_symbol": "[\"Dspp\"]", "do": "[{\"label\":\"dentinogenesis imperfecta\",\"id\":\"DOID:4154\"},{\"label\":\"periodontal disease\",\"id\":\"DOID:3388\"}]" }, { "gene_id": 666339, "description": "mucin 17, cell surface associated", "gene_symbol": "[\"Muc17\"]", "do": null }, { "gene_id": 667277, "description": "complement component 1, r subcomponent B", "gene_symbol": "[\"C1rb\"]", "do": null }, { "gene_id": 667281, "description": "histocompatibility 60b", "gene_symbol": "[\"H60b\"]", "do": null }, { "gene_id": 667742, "description": "piezo-type mechanosensitive ion channel component 2", "gene_symbol": "[\"Piezo2\"]", "do": null }, { "gene_id": 667823, "description": "tripartite motif-containing 5", "gene_symbol": "[\"Trim5\"]", "do": null }, { "gene_id": 667977, "description": "histocompatibility 2, T region locus 26", "gene_symbol": "[\"H2-T26\"]", "do": null }, { "gene_id": 667992, "description": "taste receptor, type 2, member 103", "gene_symbol": "[\"Tas2r103\"]", "do": null }, { "gene_id": 668101, "description": "signal-regulatory protein beta 1B", "gene_symbol": "[\"Sirpb1b\"]", "do": null }, { "gene_id": 668940, "description": "myosin, heavy chain 7B, cardiac muscle, beta", "gene_symbol": "[\"Myh7b\"]", "do": null }, { "gene_id": 670558, "description": "histocompatibility 60c", "gene_symbol": "[\"H60c\"]", "do": null }, { "gene_id": 671232, "description": "testis and ovary specific PAZ domain containing 1", "gene_symbol": "[\"Topaz1\"]", "do": null }, { "gene_id": 671535, "description": "poly (ADP-ribose) polymerase family, member 10", "gene_symbol": "[\"Parp10\"]", "do": null }, { "gene_id": 672511, "description": "ring finger protein 213", "gene_symbol": "[\"Rnf213\"]", "do": null }, { "gene_id": 677296, "description": "Fc receptor-like 6", "gene_symbol": "[\"Fcrl6\"]", "do": null }, { "gene_id": 677884, "description": "paralemmin A kinase anchor protein", "gene_symbol": "[\"Pakap\"]", "do": null }, { "gene_id": 751865, "description": "Sin3A associated protein 25", "gene_symbol": "[\"Sap25\"]", "do": null }, { "gene_id": 100037283, "description": "ribonuclease T2A", "gene_symbol": "[\"Rnaset2a\"]", "do": null }, { "gene_id": 100038347, "description": "family with sequence similarity 174, member B", "gene_symbol": "[\"Fam174b\"]", "do": null }, { "gene_id": 100038417, "description": "serine peptidase inhibitor, Kazal type 13", "gene_symbol": "[\"Spink13\"]", "do": null }, { "gene_id": 100038909, "description": "paired-Ig-like receptor A12", "gene_symbol": "[\"Pira12\"]", "do": null }, { "gene_id": 100038947, "description": "signal-regulatory protein beta 1C", "gene_symbol": "[\"Sirpb1c\"]", "do": null }, { "gene_id": 100039953, "description": "golgi-associated olfactory signaling regulator", "gene_symbol": "[\"Gfy\"]", "do": null }, { "gene_id": 100041230, "description": "H4 clustered histone 17", "gene_symbol": "[\"H4c17\"]", "do": null }, { "gene_id": 100041296, "description": "PRAME like 47", "gene_symbol": "[\"Pramel47\"]", "do": null }, { "gene_id": 100041596, "description": "galactose-3-O-sulfotransferase 2B", "gene_symbol": "[\"Gal3st2b\"]", "do": null }, { "gene_id": 100042480, "description": "NHS like 2", "gene_symbol": "[\"Nhsl2\"]", "do": null }, { "gene_id": 100043207, "description": "amylase 2a1", "gene_symbol": "[\"Amy2a1\"]", "do": null }, { "gene_id": 100043684, "description": "amylase 2a4", "gene_symbol": "[\"Amy2a4\"]", "do": null }, { "gene_id": 100043686, "description": "amylase 2a3", 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channel, voltage-dependent, beta subunit associated regulatory protein", "gene_symbol": "[\"Cbarp\"]", "do": null }, { "gene_id": 100503895, "description": "tryptase alpha/beta 1", "gene_symbol": "[\"Tpsab1\"]", "do": null }, { "gene_id": 100504404, "description": "histocompatibility 2, class II antigen E alpha", "gene_symbol": "[\"H2-Ea\"]", "do": null }, { "gene_id": 100504663, "description": "autophagy related 14", "gene_symbol": "[\"Atg14\"]", "do": null }, { "gene_id": 100529082, "description": "histocompatibility 2, T region locus 27", "gene_symbol": "[\"H2-T27\"]", "do": null }, { "gene_id": 101055671, "description": "lipase, member O2", "gene_symbol": "[\"Lipo2\"]", "do": null }, { "gene_id": 102635496, "description": "MAM and LDL receptor class A domain containing 1", "gene_symbol": "[\"Malrd1\"]", "do": null }, { "gene_id": 110599584, "description": "Eef1akmt4-endothelin converting enzyme 2 readthrough", "gene_symbol": "[\"Eef1ece2\"]", "do": null }, { "gene_id": 116621581, "description": "DERPC proline and glycine rich nuclear protein", "gene_symbol": "[\"Derpc\"]", "do": null } ]