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:1459 | hypothyroidism | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:2513 | basal cell carcinoma | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:0080171 | esophageal atresia/tracheoesophageal fistula | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:10534 | stomach cancer | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:0050424 | familial adenomatous polyposis | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:0111564 | hypoplastic or aplastic tibia with polydactyly | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:0110964 | brachydactyly type A1 | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:13608 | biliary atresia | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:0111816 | syndactyly type 1 | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:1312 | focal segmental glomerulosclerosis | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:14448 | 46,XY sex reversal | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:10487 | Hirschsprung's disease | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:0080855 | Parkinsonism | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:0060041 | autism spectrum disorder | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:8398 | osteoarthritis | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:2377 | multiple sclerosis | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:784 | chronic kidney disease | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:9282 | ocular hypertension | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:10976 | membranous glomerulonephritis | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:9253 | gastrointestinal stromal tumor | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:0060850 | annular pancreas | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:3328 | temporal lobe epilepsy | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:3525 | middle cerebral artery infarction | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:14679 | VACTERL association | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:4621 | holoprosencephaly | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-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 v4.1.0
Last updated: December 9, 2024