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:2340 | craniosynostosis | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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DOID:0080787 | proximal symphalangism 1 | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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DOID:12556 | acute kidney tubular necrosis | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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DOID:0110975 | brachydactyly type B2 | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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DOID:0050789 | tarsal-carpal coalition syndrome | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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DOID:0080329 | cold-induced sweating syndrome 1 | HGNC:2364 | Homo sapiens (human) | 9244 | CRLF1 |
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DOID:0014667 | disease of metabolism | HGNC:21481 | Homo sapiens (human) | 92483 | LDHAL6B |
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DOID:635 | acquired immunodeficiency syndrome | HGNC:1706 | Homo sapiens (human) | 925 | CD8A |
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DOID:0050185 | erythema multiforme | HGNC:1706 | Homo sapiens (human) | 925 | CD8A |
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DOID:3454 | brain infarction | HGNC:1706 | Homo sapiens (human) | 925 | CD8A |
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DOID:10534 | stomach cancer | HGNC:1706 | Homo sapiens (human) | 925 | CD8A |
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DOID:612 | primary immunodeficiency disease | HGNC:1706 | Homo sapiens (human) | 925 | CD8A |
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DOID:670 | amphetamine abuse | HGNC:1706 | Homo sapiens (human) | 925 | CD8A |
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DOID:0080600 | COVID-19 | HGNC:1706 | Homo sapiens (human) | 925 | CD8A |
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DOID:1319 | brain cancer | HGNC:8061 | Homo sapiens (human) | 9253 | NUMBL |
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DOID:1826 | epilepsy | HGNC:1400 | Homo sapiens (human) | 9254 | CACNA2D2 |
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DOID:0060790 | hypomyelinating leukodystrophy 3 | HGNC:10648 | Homo sapiens (human) | 9255 | AIMP1 |
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DOID:1289 | neurodegenerative disease | HGNC:10648 | Homo sapiens (human) | 9255 | AIMP1 |
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DOID:5844 | myocardial infarction | HGNC:10648 | Homo sapiens (human) | 9255 | AIMP1 |
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DOID:0112136 | severe congenital neutropenia 4 | HGNC:24861 | Homo sapiens (human) | 92579 | G6PC3 |
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DOID:4415 | fibrous histiocytoma | HGNC:16982 | Homo sapiens (human) | 9258 | MFHAS1 |
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DOID:423 | myopathy | HGNC:22958 | Homo sapiens (human) | 9260 | PDLIM7 |
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DOID:0080095 | myofibrillar myopathy 4 | HGNC:22958 | Homo sapiens (human) | 9260 | PDLIM7 |
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DOID:0050700 | cardiomyopathy | HGNC:22958 | Homo sapiens (human) | 9260 | PDLIM7 |
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DOID:12930 | dilated cardiomyopathy | HGNC:24456 | Homo sapiens (human) | 92737 | DNER |
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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