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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:6432 | pulmonary hypertension | HGNC:11009 | Homo sapiens (human) | 6517 | SLC2A4 |
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| DOID:583 | hemolytic anemia | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:9471 | meningitis | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:0050700 | cardiomyopathy | HGNC:4432 | Homo sapiens (human) | 2805 | GOT1 |
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| DOID:0111265 | Boucher-Neuhauser syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0014667 | disease of metabolism | HGNC:9021 | Homo sapiens (human) | 5315 | PKM |
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| DOID:14749 | methylmalonic acidemia | HGNC:7526 | Homo sapiens (human) | 4594 | MMUT |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:576 | proteinuria | HGNC:10658 | Homo sapiens (human) | 6382 | SDC1 |
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| DOID:13250 | diarrhea | HGNC:6530 | Homo sapiens (human) | 3938 | LCT |
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| DOID:14330 | Parkinson's disease | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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| DOID:13241 | Behcet's disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0014667 | disease of metabolism | HGNC:2898 | Homo sapiens (human) | 1738 | DLD |
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| DOID:2741 | bilirubin metabolic disorder | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:0050741 | alcohol dependence | HGNC:250 | Homo sapiens (human) | 125 | ADH1B |
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| DOID:1596 | depressive disorder | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:7998 | hyperthyroidism | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:10763 | hypertension | HGNC:20575 | Homo sapiens (human) | 284541 | CYP4A22 |
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| DOID:2394 | ovarian cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:574 | peripheral nervous system disease | HGNC:6719 | Homo sapiens (human) | 4056 | LTC4S |
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| DOID:2977 | primary hyperoxaluria | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:219 | colon cancer | HGNC:9376 | Homo sapiens (human) | 5562 | PRKAA1 |
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| DOID:1612 | breast cancer | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:10652 | Alzheimer's disease | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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