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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources July 29, 2024
Displaying entries 4401 - 4425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence Code Names References
DOID:4450 renal cell carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:17094408
DOID:6498 seborrheic keratosis MGI:1206581 Mus musculus (house mouse) 18706 Pik3ca
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:17290104
  • PMID:20486200
DOID:5844 myocardial infarction HGNC:4799 Homo sapiens (human) 3033 HADH
  • MGI:6194238
DOID:11506 suppurative otitis media FB:FBgn0262473 Drosophila melanogaster (fruit fly) 43222 Tl
  • MGI:6194238
DOID:0060841 isolated microphthalmia 8 HGNC:409 Homo sapiens (human) 220 ALDH1A3
  • RGD:7240710
DOID:5419 schizophrenia ZFIN:ZDB-GENE-040801-191 Danio rerio (zebrafish) 445060 b3gat2
  • MGI:6194238
DOID:8719 in situ carcinoma HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • PMID:8649861
DOID:0110295 autosomal recessive limb-girdle muscular dystrophy type 2U HGNC:37276 Homo sapiens (human) 729920 CRPPA
  • MGI:6194238
  • RGD:7240710
DOID:0060256 Dowling-Degos disease HGNC:22954 Homo sapiens (human) 56983 POGLUT1
  • RGD:7240710
DOID:2841 asthma RGD:620874 Rattus norvegicus (Norway rat) 89824 Chi3l1
  • MGI:6194238
DOID:4029 gastritis MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:13608 biliary atresia HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:29056230
DOID:3910 lung adenocarcinoma SGD:S000005646 Saccharomyces cerevisiae S288C 854287 GCY1
  • MGI:6194238
DOID:2747 glycogen storage disease MGI:2385254 Mus musculus (house mouse) 232493 Gys2
  • MGI:6194238
DOID:2913 acute pancreatitis HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:7998 hyperthyroidism WB:WBGene00010904 Caenorhabditis elegans 175591 ugt-62
  • MGI:6194238
DOID:1062 Fanconi syndrome HGNC:11006 Homo sapiens (human) 6514 SLC2A2
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:11009 Homo sapiens (human) 6517 SLC2A4
  • PMID:18778861
DOID:206 hereditary multiple exostoses WB:WBGene00004361 Caenorhabditis elegans 176502 rib-2
  • PMID:17237233
DOID:11446 sciatic neuropathy HGNC:14076 Homo sapiens (human) 29956 CERS2
  • MGI:6194238
DOID:10241 thalassemia RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:10825 essential hypertension HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • RGD:7240710
DOID:11121 pulpitis RGD:3870 Rattus norvegicus (Norway rat) 29260 Tlr4
  • PMID:24267924
DOID:1287 cardiovascular system disease HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • PMID:21282363

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024