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:13641 | exfoliation syndrome | WB:WBGene00010775 | Caenorhabditis elegans | 187297 | poml-1 |
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DOID:1040 | chronic lymphocytic leukemia | WB:WBGene00010775 | Caenorhabditis elegans | 187297 | poml-1 |
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DOID:1067 | open-angle glaucoma | WB:WBGene00010775 | Caenorhabditis elegans | 187297 | poml-1 |
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DOID:11713 | diabetic angiopathy | WB:WBGene00010775 | Caenorhabditis elegans | 187297 | poml-1 |
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DOID:0110219 | Brugada syndrome 2 | WB:WBGene00010778 | Caenorhabditis elegans | 176399 | gpdh-2 |
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DOID:783 | end stage renal disease | WB:WBGene00010872 | Caenorhabditis elegans | 172457 | plag-15 |
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DOID:2349 | arteriosclerosis | WB:WBGene00010872 | Caenorhabditis elegans | 172457 | plag-15 |
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DOID:1391 | Norum disease | WB:WBGene00010872 | Caenorhabditis elegans | 172457 | plag-15 |
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DOID:5844 | myocardial infarction | WB:WBGene00010872 | Caenorhabditis elegans | 172457 | plag-15 |
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DOID:1168 | familial hyperlipidemia | WB:WBGene00010872 | Caenorhabditis elegans | 172457 | plag-15 |
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DOID:2741 | bilirubin metabolic disorder | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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DOID:7998 | hyperthyroidism | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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DOID:9352 | type 2 diabetes mellitus | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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DOID:9744 | type 1 diabetes mellitus | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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DOID:3803 | Crigler-Najjar syndrome | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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DOID:783 | end stage renal disease | WB:WBGene00011076 | Caenorhabditis elegans | 181200 | scav-5 |
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DOID:891 | progressive myoclonus epilepsy | WB:WBGene00011076 | Caenorhabditis elegans | 181200 | scav-5 |
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DOID:3211 | lysosomal storage disease | WB:WBGene00011095 | Caenorhabditis elegans | 179660 | gana-1 |
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DOID:14499 | Fabry disease | WB:WBGene00011095 | Caenorhabditis elegans | 179660 | gana-1 |
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DOID:0112319 | Kanzaki disease | WB:WBGene00011095 | Caenorhabditis elegans | 179660 | gana-1 |
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DOID:2367 | neuroaxonal dystrophy | WB:WBGene00011095 | Caenorhabditis elegans | 179660 | gana-1 |
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DOID:479 | angiokeratoma | WB:WBGene00011095 | Caenorhabditis elegans | 179660 | gana-1 |
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DOID:0112318 | Schindler disease type 1 | WB:WBGene00011095 | Caenorhabditis elegans | 179660 | gana-1 |
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DOID:0080470 | developmental and epileptic encephalopathy 36 | WB:WBGene00011193 | Caenorhabditis elegans | 179890 | algn-13 |
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DOID:0080411 | familial adenomatous polyposis 3 | WB:WBGene00011201 | Caenorhabditis elegans | 187770 | nth-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