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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▲ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:11132 | prostatic hypertrophy | HGNC:30620 | Homo sapiens (human) | 80310 | PDGFD |
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| DOID:4783 | mesangial proliferative glomerulonephritis | HGNC:30620 | Homo sapiens (human) | 80310 | PDGFD |
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| DOID:5082 | liver cirrhosis | HGNC:30620 | Homo sapiens (human) | 80310 | PDGFD |
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| DOID:2921 | glomerulonephritis | HGNC:30620 | Homo sapiens (human) | 80310 | PDGFD |
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| DOID:1936 | atherosclerosis | HGNC:30620 | Homo sapiens (human) | 80310 | PDGFD |
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| DOID:684 | hepatocellular carcinoma | HGNC:29484 | Homo sapiens (human) | 80312 | TET1 |
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| DOID:12236 | primary biliary cholangitis | HGNC:21747 | Homo sapiens (human) | 80315 | CPEB4 |
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| DOID:10762 | portal hypertension | HGNC:21747 | Homo sapiens (human) | 80315 | CPEB4 |
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| DOID:5082 | liver cirrhosis | HGNC:21747 | Homo sapiens (human) | 80315 | CPEB4 |
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| DOID:0111647 | Schopf-Schulz-Passarge syndrome | HGNC:13829 | Homo sapiens (human) | 80326 | WNT10A |
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| DOID:0050591 | tooth agenesis | HGNC:13829 | Homo sapiens (human) | 80326 | WNT10A |
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| DOID:2121 | ectodermal dysplasia | HGNC:13829 | Homo sapiens (human) | 80326 | WNT10A |
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| DOID:2841 | asthma | HGNC:15478 | Homo sapiens (human) | 80332 | ADAM33 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:15478 | Homo sapiens (human) | 80332 | ADAM33 |
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| DOID:4483 | rhinitis | HGNC:15478 | Homo sapiens (human) | 80332 | ADAM33 |
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| DOID:1459 | hypothyroidism | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0060158 | acquired metabolic disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0050729 | Chanarin-Dorfman syndrome | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:9970 | obesity | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:3393 | coronary artery disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:9452 | steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:5082 | liver cirrhosis | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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