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:0050742 | nicotine dependence | HGNC:2345 | Homo sapiens (human) | 1385 | CREB1 |
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DOID:9973 | substance dependence | HGNC:2345 | Homo sapiens (human) | 1385 | CREB1 |
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DOID:11206 | opioid abuse | HGNC:2345 | Homo sapiens (human) | 1385 | CREB1 |
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DOID:12858 | Huntington's disease | HGNC:2345 | Homo sapiens (human) | 1385 | CREB1 |
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DOID:3525 | middle cerebral artery infarction | HGNC:2345 | Homo sapiens (human) | 1385 | CREB1 |
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DOID:9975 | cocaine dependence | HGNC:2345 | Homo sapiens (human) | 1385 | CREB1 |
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DOID:10933 | obsessive-compulsive disorder | HGNC:2345 | Homo sapiens (human) | 1385 | CREB1 |
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DOID:9976 | heroin dependence | HGNC:2345 | Homo sapiens (human) | 1385 | CREB1 |
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DOID:10763 | hypertension | HGNC:2345 | Homo sapiens (human) | 1385 | CREB1 |
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DOID:10584 | retinitis pigmentosa | HGNC:18688 | Homo sapiens (human) | 286204 | CRB2 |
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DOID:0111134 | focal segmental glomerulosclerosis 9 | HGNC:18688 | Homo sapiens (human) | 286204 | CRB2 |
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DOID:0111625 | ventriculomegaly - cystic kidney disease | HGNC:18688 | Homo sapiens (human) | 286204 | CRB2 |
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DOID:10584 | retinitis pigmentosa | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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DOID:14791 | Leber congenital amaurosis | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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DOID:0110079 | Leber congenital amaurosis 8 | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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DOID:0111541 | pigmented paravenous chorioretinal atrophy | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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DOID:0110358 | retinitis pigmentosa 12 | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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DOID:0050572 | cone-rod dystrophy | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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DOID:0110734 | neurodegeneration with brain iron accumulation | HGNC:2342 | Homo sapiens (human) | 1384 | CRAT |
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DOID:0081150 | common variable immunodeficiency 7 | HGNC:2336 | Homo sapiens (human) | 1380 | CR2 |
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DOID:526 | human immunodeficiency virus infectious disease | HGNC:2336 | Homo sapiens (human) | 1380 | CR2 |
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DOID:9261 | nasopharynx carcinoma | HGNC:2336 | Homo sapiens (human) | 1380 | CR2 |
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DOID:9074 | systemic lupus erythematosus | HGNC:2336 | Homo sapiens (human) | 1380 | CR2 |
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DOID:12365 | malaria | HGNC:2334 | Homo sapiens (human) | 1378 | CR1 |
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DOID:3146 | lipid metabolism disorder | FB:FBgn0035383 | Drosophila melanogaster (fruit fly) | 38355 | CPT2 |
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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