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:10579 | leukodystrophy | HGNC:16066 | Homo sapiens (human) | 55331 | ACER3 |
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DOID:437 | myasthenia gravis | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:12858 | Huntington's disease | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:2377 | multiple sclerosis | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:1826 | epilepsy | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:2297 | leptospirosis | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:6088 | acute stress disorder | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:9744 | type 1 diabetes mellitus | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:10652 | Alzheimer's disease | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:10487 | Hirschsprung's disease | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:9470 | bacterial meningitis | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:14330 | Parkinson's disease | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:331 | central nervous system disease | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
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DOID:13268 | porphyria | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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DOID:14330 | Parkinson's disease | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
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DOID:1289 | neurodegenerative disease | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
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DOID:0111442 | optic atrophy 9 | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
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DOID:1891 | optic nerve disease | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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DOID:0050883 | infantile cerebellar-retinal degeneration | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
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DOID:1724 | duodenal ulcer | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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DOID:331 | central nervous system disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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DOID:0111442 | optic atrophy 9 | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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DOID:14330 | Parkinson's disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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DOID:1289 | neurodegenerative disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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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