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 | October 9, 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:636 | central pontine myelinolysis | HGNC:637 | Homo sapiens (human) | 361 | AQP4 |
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DOID:1727 | retinal vein occlusion | HGNC:637 | Homo sapiens (human) | 361 | AQP4 |
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DOID:2316 | brain ischemia | HGNC:637 | Homo sapiens (human) | 361 | AQP4 |
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DOID:0080122 | Alpers-Huttenlocher syndrome | HGNC:637 | Homo sapiens (human) | 361 | AQP4 |
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DOID:224 | transient cerebral ischemia | HGNC:637 | Homo sapiens (human) | 361 | AQP4 |
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DOID:1459 | hypothyroidism | HGNC:636 | Homo sapiens (human) | 360 | AQP3 |
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DOID:2316 | brain ischemia | HGNC:636 | Homo sapiens (human) | 360 | AQP3 |
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DOID:12387 | nephrogenic diabetes insipidus | HGNC:636 | Homo sapiens (human) | 360 | AQP3 |
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DOID:4724 | brain edema | HGNC:636 | Homo sapiens (human) | 360 | AQP3 |
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DOID:0081061 | nephrogenic diabetes insipidus type 2 | HGNC:634 | Homo sapiens (human) | 359 | AQP2 |
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DOID:10763 | hypertension | HGNC:634 | Homo sapiens (human) | 359 | AQP2 |
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DOID:9409 | diabetes insipidus | HGNC:634 | Homo sapiens (human) | 359 | AQP2 |
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DOID:1837 | diabetic ketoacidosis | HGNC:634 | Homo sapiens (human) | 359 | AQP2 |
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DOID:12387 | nephrogenic diabetes insipidus | HGNC:634 | Homo sapiens (human) | 359 | AQP2 |
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DOID:10763 | hypertension | HGNC:633 | Homo sapiens (human) | 358 | AQP1 |
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DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:633 | Homo sapiens (human) | 358 | AQP1 |
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DOID:13141 | uveitis | HGNC:633 | Homo sapiens (human) | 358 | AQP1 |
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DOID:636 | central pontine myelinolysis | HGNC:633 | Homo sapiens (human) | 358 | AQP1 |
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DOID:4724 | brain edema | HGNC:633 | Homo sapiens (human) | 358 | AQP1 |
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DOID:1727 | retinal vein occlusion | HGNC:633 | Homo sapiens (human) | 358 | AQP1 |
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DOID:10908 | hydrocephalus | HGNC:633 | Homo sapiens (human) | 358 | AQP1 |
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DOID:9351 | diabetes mellitus | HGNC:633 | Homo sapiens (human) | 358 | AQP1 |
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DOID:9428 | intracranial hypertension | HGNC:633 | Homo sapiens (human) | 358 | AQP1 |
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DOID:1824 | status epilepticus | HGNC:633 | Homo sapiens (human) | 358 | AQP1 |
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DOID:14784 | olivopontocerebellar atrophy | HGNC:15984 | Homo sapiens (human) | 54840 | APTX |
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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 v4.1.0
Last updated: December 9, 2024