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:0111380 | solitary median maxillary central incisor | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:0050784 | primary progressive multiple sclerosis | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:2512 | nevoid basal cell carcinoma syndrome | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:5844 | myocardial infarction | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:0111818 | syndactyly type 4 | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:0110875 | holoprosencephaly 3 | WB:WBGene00001691 | Caenorhabditis elegans | 180349 | grd-2 |
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DOID:0080042 | autosomal recessive spinocerebellar ataxia 18 | ZFIN:ZDB-GENE-040913-1 | Danio rerio (zebrafish) | 448841 | grid2 |
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DOID:3526 | cerebral infarction | Xenbase:XB-GENE-866327 | Xenopus laevis (African clawed frog) | 397953 | grin1.L |
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DOID:0070387 | developmental and epileptic encephalopathy 101 | Xenbase:XB-GENE-866327 | Xenopus laevis (African clawed frog) | 397953 | grin1.L |
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DOID:11206 | opioid abuse | Xenbase:XB-GENE-866327 | Xenopus laevis (African clawed frog) | 397953 | grin1.L |
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DOID:1574 | alcohol use disorder | Xenbase:XB-GENE-866327 | Xenopus laevis (African clawed frog) | 397953 | grin1.L |
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DOID:10652 | Alzheimer's disease | Xenbase:XB-GENE-866327 | Xenopus laevis (African clawed frog) | 397953 | grin1.L |
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DOID:8725 | vascular dementia | Xenbase:XB-GENE-866327 | Xenopus laevis (African clawed frog) | 397953 | grin1.L |
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DOID:0070038 | autosomal dominant intellectual developmental disorder 8 | Xenbase:XB-GENE-866327 | Xenopus laevis (African clawed frog) | 397953 | grin1.L |
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DOID:0070038 | autosomal dominant intellectual developmental disorder 8 | Xenbase:XB-GENE-17335935 | Xenopus laevis (African clawed frog) | 108699855 | grin1.S |
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DOID:1574 | alcohol use disorder | Xenbase:XB-GENE-17335935 | Xenopus laevis (African clawed frog) | 108699855 | grin1.S |
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DOID:10652 | Alzheimer's disease | Xenbase:XB-GENE-17335935 | Xenopus laevis (African clawed frog) | 108699855 | grin1.S |
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DOID:0070387 | developmental and epileptic encephalopathy 101 | Xenbase:XB-GENE-17335935 | Xenopus laevis (African clawed frog) | 108699855 | grin1.S |
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DOID:8725 | vascular dementia | Xenbase:XB-GENE-17335935 | Xenopus laevis (African clawed frog) | 108699855 | grin1.S |
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DOID:11206 | opioid abuse | Xenbase:XB-GENE-17335935 | Xenopus laevis (African clawed frog) | 108699855 | grin1.S |
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DOID:3526 | cerebral infarction | Xenbase:XB-GENE-17335935 | Xenopus laevis (African clawed frog) | 108699855 | grin1.S |
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DOID:9261 | nasopharynx carcinoma | Xenbase:XB-GENE-1021446 | Xenopus laevis (African clawed frog) | 100127346 | grin2a.L |
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DOID:12858 | Huntington's disease | Xenbase:XB-GENE-1021446 | Xenopus laevis (African clawed frog) | 100127346 | grin2a.L |
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DOID:10652 | Alzheimer's disease | Xenbase:XB-GENE-1021446 | Xenopus laevis (African clawed frog) | 100127346 | grin2a.L |
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DOID:8725 | vascular dementia | Xenbase:XB-GENE-1021446 | Xenopus laevis (African clawed frog) | 100127346 | grin2a.L |
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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