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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:0050809 | mucopolysaccharidosis IX | HGNC:5320 | Homo sapiens (human) | 3373 | HYAL1 |
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| DOID:3121 | gallbladder cancer | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:9427 | hypertensive encephalopathy | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:9119 | acute myeloid leukemia | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:418 | systemic scleroderma | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:14264 | benign neonatal seizures | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0110980 | Joubert syndrome 1 | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:12351 | alcoholic hepatitis | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:1561 | cognitive disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:1793 | pancreatic cancer | HGNC:7413 | Homo sapiens (human) | 4507 | MTAP |
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| DOID:9273 | citrullinemia | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:8947 | diabetic retinopathy | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:0050663 | Bethlem myopathy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0080855 | Parkinsonism | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:653 | purine-pyrimidine metabolic disorder | HGNC:7892 | Homo sapiens (human) | 4860 | PNP |
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| DOID:573 | nerve compression syndrome | HGNC:6783 | Homo sapiens (human) | 4099 | MAG |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:1380 | endometrial cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:9970 | obesity | HGNC:24865 | Homo sapiens (human) | 57678 | GPAM |
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| DOID:219 | colon cancer | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:37 | skin disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080932 | primary localized cutaneous amyloidosis 3 | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:3021 | acute kidney failure | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:1168 | familial hyperlipidemia | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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