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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:0050598 | extrapulmonary tuberculosis | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:0081120 | Graves ophthalmopathy | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0080572 | congenital disorder of glycosylation Iw | HGNC:30611 | Homo sapiens (human) | 201595 | STT3B |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:10763 | hypertension | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:10763 | hypertension | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:3454 | brain infarction | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:11717 | neonatal diabetes | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:3500 | gallbladder adenocarcinoma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3669 | intermittent claudication | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:5394 | prolactinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:14330 | Parkinson's disease | HGNC:6876 | Homo sapiens (human) | 1432 | MAPK14 |
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| DOID:10652 | Alzheimer's disease | HGNC:11007 | Homo sapiens (human) | 6515 | SLC2A3 |
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| DOID:783 | end stage renal disease | HGNC:6522 | Homo sapiens (human) | 3931 | LCAT |
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| DOID:9146 | visceral leishmaniasis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:224 | transient cerebral ischemia | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:162 | cancer | HGNC:12009 | Homo sapiens (human) | 7167 | TPI1 |
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| DOID:0080599 | Coronavirus infectious disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9351 | diabetes mellitus | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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| DOID:1073 | renal hypertension | HGNC:2622 | Homo sapiens (human) | 1558 | CYP2C8 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:2986 | IgA glomerulonephritis | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:1289 | neurodegenerative disease | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:10003 | sensorineural hearing loss | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:1712 | aortic valve stenosis | HGNC:3354 | Homo sapiens (human) | 2027 | ENO3 |
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