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:526 | human immunodeficiency virus infectious disease | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:1824 | status epilepticus | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:8577 | ulcerative colitis | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:4481 | allergic rhinitis | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:10939 | antisocial personality disorder | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:684 | hepatocellular carcinoma | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:2987 | familial mediterranean fever | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:2957 | pulmonary tuberculosis | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:1168 | familial hyperlipidemia | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:12365 | malaria | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:2154 | nephroblastoma | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:2917 | cryoglobulinemia | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:0060750 | familial temporal lobe epilepsy 3 | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:13413 | hepatic encephalopathy | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:783 | end stage renal disease | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:3328 | temporal lobe epilepsy | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:635 | acquired immunodeficiency syndrome | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:0111364 | Alzheimer's disease 9 | HGNC:37 | Homo sapiens (human) | 10347 | ABCA7 |
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DOID:0050817 | Stargardt disease | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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DOID:0110015 | age related macular degeneration 2 | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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DOID:4448 | macular degeneration | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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DOID:8501 | fundus dystrophy | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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DOID:0110354 | retinitis pigmentosa 19 | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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DOID:8466 | retinal degeneration | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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DOID:0111013 | cone-rod dystrophy 3 | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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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