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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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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 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:1059 | intellectual disability | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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| DOID:9452 | steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0112349 | hereditary spastic paraplegia 81 | HGNC:29361 | Homo sapiens (human) | 85465 | SELENOI |
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| DOID:0080459 | developmental and epileptic encephalopathy 12 | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:3717 | gastric adenocarcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0080762 | autosomal recessive limb-girdle muscular dystrophy type 2Z | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:13078 | eumycotic mycetoma | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0081120 | Graves ophthalmopathy | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:8970 | subacute sclerosing panencephalitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3393 | coronary artery disease | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:684 | hepatocellular carcinoma | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:0110444 | dilated cardiomyopathy 1X | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0112237 | lissencephaly 1 | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:3132 | porphyria cutanea tarda | HGNC:2596 | Homo sapiens (human) | 1544 | CYP1A2 |
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| DOID:0110479 | autosomal recessive nonsyndromic deafness 21 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:10933 | obsessive-compulsive disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0110961 | atypical Gaucher's disease due to saposin c deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:1324 | lung cancer | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:11400 | pyelonephritis | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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| DOID:14557 | primary pulmonary hypertension | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:252 | alcoholic psychosis | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0080081 | nonsyndromic congenital nail disorder 3 | HGNC:9060 | Homo sapiens (human) | 5333 | PLCD1 |
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