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:9870 | galactosemia | WB:WBGene00008132 | Caenorhabditis elegans | 173171 | gale-1 |
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DOID:1588 | thrombocytopenia | WB:WBGene00008132 | Caenorhabditis elegans | 173171 | gale-1 |
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DOID:0060050 | autoimmune disease of blood | WB:WBGene00008019 | Caenorhabditis elegans | 176455 | C38H2.2 |
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DOID:3633 | beta-mannosidosis | WB:WBGene00007904 | Caenorhabditis elegans | 181517 | C33G3.4 |
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DOID:0080564 | congenital disorder of glycosylation Il | WB:WBGene00007556 | Caenorhabditis elegans | 174633 | algn-9 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007556 | Caenorhabditis elegans | 174633 | algn-9 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
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DOID:0050770 | polycystic liver disease | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
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DOID:0080560 | congenital disorder of glycosylation Ih | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007435 | Caenorhabditis elegans | 182392 | algn-6 |
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DOID:0080555 | congenital disorder of glycosylation Ic | WB:WBGene00007435 | Caenorhabditis elegans | 182392 | algn-6 |
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DOID:1591 | renovascular hypertension | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:13628 | favism | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:2861 | congenital nonspherocytic hemolytic anemia | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:9279 | hyperhomocysteinemia | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:9351 | diabetes mellitus | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:0050328 | congenital hypothyroidism | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:684 | hepatocellular carcinoma | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:14067 | Plasmodium falciparum malaria | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:13580 | cholestasis | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:12365 | malaria | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:83 | cataract | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:224 | transient cerebral ischemia | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:2383 | neonatal jaundice | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:5844 | myocardial infarction | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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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