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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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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:0081219 | autosomal recessive intellectual developmental disorder 57 | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
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| DOID:1380 | endometrial cancer | HGNC:2596 | Homo sapiens (human) | 1544 | CYP1A2 |
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| DOID:12306 | vitiligo | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:1485 | cystic fibrosis | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:10763 | hypertension | HGNC:6080 | Homo sapiens (human) | 3636 | INPPL1 |
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| DOID:0111334 | congenital leptin deficiency | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:0070254 | congenital disorder of glycosylation type IIb | HGNC:24862 | Homo sapiens (human) | 7841 | MOGS |
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| DOID:1793 | pancreatic cancer | HGNC:251 | Homo sapiens (human) | 126 | ADH1C |
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| DOID:1287 | cardiovascular system disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:0112250 | Gaucher's disease type IIIC | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:2526 | prostate adenocarcinoma | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:9452 | steatotic liver disease | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0110960 | Gaucher's disease perinatal lethal | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:684 | hepatocellular carcinoma | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:674 | cleft palate | HGNC:10659 | Homo sapiens (human) | 6383 | SDC2 |
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| DOID:341 | peripheral vascular disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:13550 | angle-closure glaucoma | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0080855 | Parkinsonism | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:10652 | Alzheimer's disease | HGNC:24864 | Homo sapiens (human) | 26330 | GAPDHS |
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| DOID:5041 | esophageal cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:4367 | apparent mineralocorticoid excess syndrome | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:653 | purine-pyrimidine metabolic disorder | HGNC:12563 | Homo sapiens (human) | 7372 | UMPS |
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