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:670 | amphetamine abuse | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:12399 | pathological gambling | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:9976 | heroin dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:8893 | psoriasis | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:9828 | neonatal abstinence syndrome | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:11054 | urinary bladder cancer | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:0050741 | alcohol dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:1184 | nephrotic syndrome | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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DOID:0050730 | coenzyme Q10 deficiency disease | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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DOID:4752 | multiple system atrophy | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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DOID:0070238 | primary coenzyme Q10 deficiency 1 | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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DOID:10603 | glucose intolerance | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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DOID:0090129 | carnitine palmitoyltransferase I deficiency | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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DOID:9970 | obesity | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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DOID:3319 | lymphangioleiomyomatosis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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DOID:9352 | type 2 diabetes mellitus | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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DOID:12351 | alcoholic hepatitis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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DOID:783 | end stage renal disease | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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DOID:3146 | lipid metabolism disorder | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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DOID:0110818 | hereditary spastic paraplegia 73 | HGNC:18540 | Homo sapiens (human) | 126129 | CPT1C |
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DOID:0080000 | muscular disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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DOID:0080000 | muscular disease | FB:FBgn0035383 | Drosophila melanogaster (fruit fly) | 38355 | CPT2 |
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DOID:936 | brain disease | FB:FBgn0035383 | Drosophila melanogaster (fruit fly) | 38355 | CPT2 |
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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 v4.0.0
Last updated: August 19, 2024