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 | July 29, 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:9352 | type 2 diabetes mellitus | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:557 | kidney disease | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:9281 | phenylketonuria | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:2355 | anemia | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:583 | hemolytic anemia | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:9744 | type 1 diabetes mellitus | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:6713 | cerebrovascular disease | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:9970 | obesity | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:13413 | hepatic encephalopathy | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:0110645 | long QT syndrome 2 | WB:WBGene00007043 | Caenorhabditis elegans | 172855 | algn-10 |
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DOID:0050563 | nonsyndromic deafness | WB:WBGene00007043 | Caenorhabditis elegans | 172855 | algn-10 |
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DOID:0050579 | glycogen storage disease XV | WB:WBGene00006863 | Caenorhabditis elegans | 180644 | gyg-1 |
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DOID:332 | amyotrophic lateral sclerosis | WB:WBGene00006575 | Caenorhabditis elegans | 175502 | tir-1 |
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DOID:1289 | neurodegenerative disease | WB:WBGene00006575 | Caenorhabditis elegans | 175502 | tir-1 |
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DOID:0080575 | Larsen-like syndrome B3GAT3 type | WB:WBGene00005026 | Caenorhabditis elegans | 174517 | sqv-8 |
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DOID:9206 | Barrett's esophagus | WB:WBGene00005026 | Caenorhabditis elegans | 174517 | sqv-8 |
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DOID:5419 | schizophrenia | WB:WBGene00005026 | Caenorhabditis elegans | 174517 | sqv-8 |
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DOID:3770 | pulmonary fibrosis | WB:WBGene00005026 | Caenorhabditis elegans | 174517 | sqv-8 |
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DOID:0050775 | schneckenbecken dysplasia | WB:WBGene00005025 | Caenorhabditis elegans | 174145 | sqv-7 |
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DOID:2738 | pseudoxanthoma elasticum | WB:WBGene00005024 | Caenorhabditis elegans | 190099 | sqv-6 |
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DOID:0060462 | Desbuquois dysplasia | WB:WBGene00005024 | Caenorhabditis elegans | 190099 | sqv-6 |
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DOID:557 | kidney disease | WB:WBGene00005024 | Caenorhabditis elegans | 190099 | sqv-6 |
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DOID:9744 | type 1 diabetes mellitus | WB:WBGene00005024 | Caenorhabditis elegans | 190099 | sqv-6 |
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DOID:0080322 | polycystic kidney disease | WB:WBGene00005024 | Caenorhabditis elegans | 190099 | sqv-6 |
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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 v4.0.0
Last updated: August 19, 2024