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 |
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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 |
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DOID:409 | liver disease | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:10763 | hypertension | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:3454 | brain infarction | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:9970 | obesity | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:0050741 | alcohol dependence | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:1793 | pancreatic cancer | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:9744 | type 1 diabetes mellitus | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:9976 | heroin dependence | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:1574 | alcohol use disorder | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:684 | hepatocellular carcinoma | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:5844 | myocardial infarction | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:9743 | diabetic neuropathy | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:14018 | alcoholic liver cirrhosis | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:14501 | Sjogren-Larsson syndrome | HGNC:405 | Homo sapiens (human) | 218 | ALDH3A1 |
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DOID:2349 | arteriosclerosis | HGNC:405 | Homo sapiens (human) | 218 | ALDH3A1 |
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DOID:14501 | Sjogren-Larsson syndrome | HGNC:403 | Homo sapiens (human) | 224 | ALDH3A2 |
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DOID:14501 | Sjogren-Larsson syndrome | HGNC:410 | Homo sapiens (human) | 221 | ALDH3B1 |
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DOID:14501 | Sjogren-Larsson syndrome | HGNC:411 | Homo sapiens (human) | 222 | ALDH3B2 |
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DOID:1826 | epilepsy | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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DOID:0060175 | succinic semialdehyde dehydrogenase deficiency | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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DOID:1826 | epilepsy | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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DOID:0080768 | pyridoxine-dependent epilepsy | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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DOID:0070519 | early-onset vitamin B6-dependent epilepsy 4 | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024