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:8893 | psoriasis | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:1926 | Gaucher's disease | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:0080855 | Parkinsonism | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:0112250 | Gaucher's disease type IIIC | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:0110957 | Gaucher's disease type I | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:0050474 | Netherton syndrome | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:0110959 | Gaucher's disease type III | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:14330 | Parkinson's disease | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:0110960 | Gaucher's disease perinatal lethal | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:0110958 | Gaucher's disease type II | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:12217 | Lewy body dementia | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:0070254 | congenital disorder of glycosylation type IIb | WB:WBGene00008775 | Caenorhabditis elegans | 177998 | mogs-1 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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DOID:5212 | congenital disorder of glycosylation | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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DOID:0080552 | congenital disorder of glycosylation Ia | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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DOID:0060227 | Adams-Oliver syndrome | WB:WBGene00010386 | Caenorhabditis elegans | 179990 | H12D21.10 |
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DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | WB:WBGene00010694 | Caenorhabditis elegans | 3565692 | bgnt-1.5 |
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DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | WB:WBGene00010694 | Caenorhabditis elegans | 3565692 | bgnt-1.5 |
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DOID:0111242 | congenital muscular dystrophy-dystroglycanopathy type A6 | WB:WBGene00010716 | Caenorhabditis elegans | 187206 | lge-1 |
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DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | WB:WBGene00010716 | Caenorhabditis elegans | 187206 | lge-1 |
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DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | WB:WBGene00010716 | Caenorhabditis elegans | 187206 | lge-1 |
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DOID:11727 | facioscapulohumeral muscular dystrophy | WB:WBGene00010716 | Caenorhabditis elegans | 187206 | lge-1 |
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DOID:5212 | congenital disorder of glycosylation | WB:WBGene00010720 | Caenorhabditis elegans | 175065 | algn-3 |
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DOID:0080556 | congenital disorder of glycosylation Id | WB:WBGene00010720 | Caenorhabditis elegans | 175065 | algn-3 |
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DOID:14250 | Down syndrome | WB:WBGene00010757 | Caenorhabditis elegans | 259529 | pad-2 |
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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