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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:11476 | osteoporosis | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:6432 | pulmonary hypertension | HGNC:4818 | Homo sapiens (human) | 3036 | HAS1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:4450 | renal cell carcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0050719 | cerebral folate receptor alpha deficiency | HGNC:3791 | Homo sapiens (human) | 2348 | FOLR1 |
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| DOID:2580 | rhizomelic chondrodysplasia punctata | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:11832 | visual epilepsy | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:4607 | biliary tract cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:10588 | adrenoleukodystrophy | HGNC:24174 | Homo sapiens (human) | 81616 | ACSBG2 |
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| DOID:11823 | hepatorenal syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9351 | diabetes mellitus | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:6432 | pulmonary hypertension | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10652 | Alzheimer's disease | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:3393 | coronary artery disease | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:9743 | diabetic neuropathy | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:11168 | anogenital venereal wart | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0112127 | HRPT-related hyperuricemia | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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| DOID:5614 | eye disease | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0050851 | glomerulosclerosis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:14453 | farmer's lung | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0110443 | dilated cardiomyopathy 1B | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0070238 | primary coenzyme Q10 deficiency 1 | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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