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:13078 | eumycotic mycetoma | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:10591 | pre-eclampsia | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:9505 | cannabis abuse | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:0060001 | withdrawal disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:9970 | obesity | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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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:0112321 | alacrima, achalasia, and impaired intellectual development syndrome | HGNC:22923 | Homo sapiens (human) | 29926 | GMPPA |
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DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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DOID:0111233 | congenital muscular dystrophy-dystroglycanopathy A14 | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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DOID:0112377 | muscular dystrophy-dystroglycanopathy type B14 | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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DOID:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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DOID:0060256 | Dowling-Degos disease | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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DOID:0080762 | autosomal recessive limb-girdle muscular dystrophy type 2Z | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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DOID:0060174 | GABA aminotransferase deficiency | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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DOID:10763 | hypertension | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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DOID:9976 | heroin dependence | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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DOID:11832 | visual epilepsy | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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DOID:0080855 | Parkinsonism | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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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