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: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:0112216 | developmental and epileptic encephalopathy 80 | WB:WBGene00194986 | Caenorhabditis elegans | 13184808 | pigb-1 |
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DOID:10112 | sleeping sickness | WB:WBGene00194986 | Caenorhabditis elegans | 13184808 | pigb-1 |
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DOID:0111626 | D-glyceric aciduria | HGNC:24247 | Homo sapiens (human) | 132158 | GLYCTK |
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DOID:3571 | liver cancer | HGNC:24436 | Homo sapiens (human) | 134526 | ACOT12 |
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DOID:0110676 | congenital myasthenic syndrome 13 | MGI:1196396 | Mus musculus (house mouse) | 13478 | Dpagt1 |
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DOID:0080562 | congenital disorder of glycosylation Ij | MGI:1196396 | Mus musculus (house mouse) | 13478 | Dpagt1 |
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DOID:0080557 | congenital disorder of glycosylation Ie | MGI:1330239 | Mus musculus (house mouse) | 13480 | Dpm1 |
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DOID:0050570 | congenital disorder of glycosylation type I | MGI:1330239 | Mus musculus (house mouse) | 13480 | Dpm1 |
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DOID:0050570 | congenital disorder of glycosylation type I | MGI:1330238 | Mus musculus (house mouse) | 13481 | Dpm2 |
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DOID:0080571 | congenital disorder of glycosylation Iu | MGI:1330238 | Mus musculus (house mouse) | 13481 | Dpm2 |
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DOID:5419 | schizophrenia | HGNC:922 | Homo sapiens (human) | 135152 | B3GAT2 |
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DOID:9206 | Barrett's esophagus | HGNC:922 | Homo sapiens (human) | 135152 | B3GAT2 |
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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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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