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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:12399 | pathological gambling | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0080037 | Worth syndrome | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0050211 | swine influenza | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:1793 | pancreatic cancer | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:0112318 | Schindler disease type 1 | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:10941 | intracranial aneurysm | HGNC:2464 | Homo sapiens (human) | 1462 | VCAN |
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| DOID:104 | bacterial infectious disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:1380 | endometrial cancer | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:9993 | hypoglycemia | HGNC:9291 | Homo sapiens (human) | 5506 | PPP1R3A |
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| DOID:11123 | Henoch-Schoenlein purpura | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0080055 | achondrogenesis type IB | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:0111352 | D-2-hydroxyglutaric aciduria 2 | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:13241 | Behcet's disease | HGNC:2860 | Homo sapiens (human) | 1717 | DHCR7 |
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| DOID:0070516 | Mitchell syndrome | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:0050650 | familial atrial fibrillation | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:0111271 | Oliver-McFarlane syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0112219 | developmental and epileptic encephalopathy 84 | HGNC:12525 | Homo sapiens (human) | 7358 | UGDH |
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| DOID:0050770 | polycystic liver disease | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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| DOID:9976 | heroin dependence | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:0080351 | CLOVES syndrome | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:9976 | heroin dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0050144 | Kartagener syndrome | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:1380 | endometrial cancer | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:648 | kuru | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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