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:585 | nephrolithiasis | WB:WBGene00003731 | Caenorhabditis elegans | 183811 | nhx-3 |
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DOID:0060777 | congenital secretory sodium diarrhea 8 | WB:WBGene00003731 | Caenorhabditis elegans | 183811 | nhx-3 |
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DOID:783 | end stage renal disease | WB:WBGene00003731 | Caenorhabditis elegans | 183811 | nhx-3 |
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DOID:783 | end stage renal disease | WB:WBGene00003736 | Caenorhabditis elegans | 178126 | nhx-9 |
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DOID:0060777 | congenital secretory sodium diarrhea 8 | WB:WBGene00003736 | Caenorhabditis elegans | 178126 | nhx-9 |
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DOID:9970 | obesity | WB:WBGene00003736 | Caenorhabditis elegans | 178126 | nhx-9 |
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DOID:10763 | hypertension | WB:WBGene00003736 | Caenorhabditis elegans | 178126 | nhx-9 |
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DOID:585 | nephrolithiasis | WB:WBGene00003736 | Caenorhabditis elegans | 178126 | nhx-9 |
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DOID:1591 | renovascular hypertension | WB:WBGene00003736 | Caenorhabditis elegans | 178126 | nhx-9 |
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DOID:12849 | autistic disorder | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:0090130 | cortical dysplasia-focal epilepsy syndrome | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:0060244 | specific language impairment | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:0060488 | Pitt-Hopkins syndrome | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:0060308 | autosomal recessive intellectual developmental disorder | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:4189 | mutism | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:0060558 | lethal congenital contracture syndrome | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:5419 | schizophrenia | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:11257 | social phobia | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:13365 | reading disorder | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:1059 | intellectual disability | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:4186 | articulation disorder | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:11832 | visual epilepsy | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:0060041 | autism spectrum disorder | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:1470 | major depressive disorder | WB:WBGene00003772 | Caenorhabditis elegans | 178167 | nlr-1 |
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DOID:9952 | acute lymphoblastic leukemia | WB:WBGene00003800 | Caenorhabditis elegans | 172813 | npp-14 |
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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