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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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Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:4988 | alcoholic pancreatitis | HGNC:12539 | Homo sapiens (human) | 54577 | UGT1A7 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12538 | Homo sapiens (human) | 54578 | UGT1A6 |
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| DOID:2043 | hepatitis B | HGNC:12538 | Homo sapiens (human) | 54578 | UGT1A6 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12531 | Homo sapiens (human) | 54575 | UGT1A10 |
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| DOID:1380 | endometrial cancer | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:8778 | Crohn's disease | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:11151 | cholecystolithiasis | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:2043 | hepatitis B | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:74 | hematopoietic system disease | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:2394 | ovarian cancer | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:2739 | Gilbert syndrome | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:8692 | myeloid leukemia | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:10211 | cholelithiasis | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:2741 | bilirubin metabolic disorder | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:1612 | breast cancer | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:3803 | Crigler-Najjar syndrome | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:7998 | hyperthyroidism | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:162 | cancer | HGNC:12527 | Homo sapiens (human) | 7360 | UGP2 |
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| DOID:0112218 | developmental and epileptic encephalopathy 83 | HGNC:12527 | Homo sapiens (human) | 7360 | UGP2 |
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| DOID:0112219 | developmental and epileptic encephalopathy 84 | HGNC:12525 | Homo sapiens (human) | 7358 | UGDH |
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| DOID:10763 | hypertension | HGNC:12524 | Homo sapiens (human) | 7357 | UGCG |
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| DOID:1289 | neurodegenerative disease | HGNC:12520 | Homo sapiens (human) | 7353 | UFD1 |
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