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:799 | varicose veins | WB:WBGene00008656 | Caenorhabditis elegans | 184307 | lron-5 |
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DOID:2566 | corneal dystrophy | WB:WBGene00008656 | Caenorhabditis elegans | 184307 | lron-5 |
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DOID:3087 | gingivitis | WB:WBGene00008656 | Caenorhabditis elegans | 184307 | lron-5 |
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DOID:824 | periodontitis | WB:WBGene00008656 | Caenorhabditis elegans | 184307 | lron-5 |
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DOID:3407 | carotid artery disease | WB:WBGene00008656 | Caenorhabditis elegans | 184307 | lron-5 |
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DOID:0060287 | cornea plana | WB:WBGene00008656 | Caenorhabditis elegans | 184307 | lron-5 |
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DOID:10126 | keratoconus | WB:WBGene00008656 | Caenorhabditis elegans | 184307 | lron-5 |
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DOID:3393 | coronary artery disease | WB:WBGene00008656 | Caenorhabditis elegans | 184307 | lron-5 |
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DOID:783 | end stage renal disease | WB:WBGene00008692 | Caenorhabditis elegans | 181429 | scav-4 |
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DOID:891 | progressive myoclonus epilepsy | WB:WBGene00008692 | Caenorhabditis elegans | 181429 | scav-4 |
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DOID:0080855 | Parkinsonism | 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:0112250 | Gaucher's disease type IIIC | 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: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:0060892 | late onset Parkinson's disease | 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:8893 | psoriasis | 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:0110960 | Gaucher's disease perinatal lethal | 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:0080540 | galactosialidosis | WB:WBGene00008741 | Caenorhabditis elegans | 174802 | ctsa-1.2 |
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DOID:3211 | lysosomal storage disease | WB:WBGene00008741 | Caenorhabditis elegans | 174802 | ctsa-1.2 |
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DOID:0070254 | congenital disorder of glycosylation type IIb | WB:WBGene00008775 | Caenorhabditis elegans | 177998 | mogs-1 |
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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