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:1852 | intrahepatic cholestasis | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:1920 | hyperuricemia | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:2841 | asthma | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:1074 | kidney failure | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:7148 | rheumatoid arthritis | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:8778 | Crohn's disease | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:783 | end stage renal disease | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:0050908 | myelodysplastic syndrome | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:6000 | congestive heart failure | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:13619 | extrahepatic cholestasis | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:14365 | systemic primary carnitine deficiency disease | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:0050700 | cardiomyopathy | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:3021 | acute kidney failure | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:655 | inherited metabolic disorder | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 1-Oct |
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DOID:14365 | systemic primary carnitine deficiency disease | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 45566 |
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DOID:2841 | asthma | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 45566 |
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DOID:7148 | rheumatoid arthritis | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 45566 |
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DOID:1852 | intrahepatic cholestasis | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 45566 |
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DOID:6000 | congestive heart failure | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 45566 |
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DOID:783 | end stage renal disease | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 45566 |
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DOID:0050908 | myelodysplastic syndrome | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 45566 |
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DOID:8778 | Crohn's disease | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 45566 |
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DOID:1920 | hyperuricemia | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 45566 |
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DOID:0050700 | cardiomyopathy | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 45566 |
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DOID:1074 | kidney failure | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 45566 |
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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