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:0050833 | orotic aciduria | WB:WBGene00020036 | Caenorhabditis elegans | 172008 | R12E2.11 |
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DOID:0060363 | glycerol kinase deficiency | WB:WBGene00020007 | Caenorhabditis elegans | 173747 | R11F4.1 |
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DOID:13810 | familial hypercholesterolemia | WB:WBGene00020007 | Caenorhabditis elegans | 173747 | R11F4.1 |
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DOID:0110658 | congenital myasthenic syndrome 15 | WB:WBGene00019725 | Caenorhabditis elegans | 187398 | algn-14 |
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DOID:2018 | hyperinsulinism | WB:WBGene00019295 | Caenorhabditis elegans | 177363 | pfkb-1.2 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00019276 | Caenorhabditis elegans | 178822 | algn-5 |
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DOID:0080322 | polycystic kidney disease | WB:WBGene00019276 | Caenorhabditis elegans | 178822 | algn-5 |
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DOID:10763 | hypertension | WB:WBGene00019127 | Caenorhabditis elegans | 174001 | cgt-3 |
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DOID:3908 | lung non-small cell carcinoma | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:4988 | alcoholic pancreatitis | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:10211 | cholelithiasis | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:2394 | ovarian cancer | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:4947 | cholangiocarcinoma | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:8778 | Crohn's disease | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:1612 | breast cancer | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:1380 | endometrial cancer | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:2043 | hepatitis B | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:3803 | Crigler-Najjar syndrome | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:2739 | Gilbert syndrome | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:1793 | pancreatic cancer | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:2741 | bilirubin metabolic disorder | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:8692 | myeloid leukemia | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:11151 | cholecystolithiasis | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:0080558 | congenital disorder of glycosylation If | WB:WBGene00018181 | Caenorhabditis elegans | 179218 | mpdu-1 |
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DOID:0050565 | autosomal recessive nonsyndromic deafness | WB:WBGene00018175 | Caenorhabditis elegans | 185454 | F38B6.6 |
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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