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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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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 | July 29, 2024 |
| 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:9238 | Homo sapiens (human) | 5471 | PPAT |
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| DOID:0070430 | combined oxidative phosphorylation deficiency 57 | HGNC:16148 | Homo sapiens (human) | 54675 | CRLS1 |
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| DOID:1793 | pancreatic cancer | HGNC:9235 | Homo sapiens (human) | 5467 | PPARD |
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| DOID:4607 | biliary tract cancer | HGNC:9235 | Homo sapiens (human) | 5467 | PPARD |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9235 | Homo sapiens (human) | 5467 | PPARD |
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| DOID:11151 | cholecystolithiasis | 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:74 | hematopoietic system disease | 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:8692 | myeloid leukemia | 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: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:10211 | cholelithiasis | 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:1380 | endometrial 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:2394 | ovarian cancer | 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: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:10908 | hydrocephalus | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:9452 | steatotic liver disease | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:5419 | schizophrenia | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:3146 | lipid metabolism disorder | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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