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: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:0050588 | muscular dystrophy-dystroglycanopathy type B1 | WB:WBGene00015982 | Caenorhabditis elegans | 182795 | bgnt-1.4 |
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DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | WB:WBGene00010716 | Caenorhabditis elegans | 187206 | lge-1 |
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DOID:0050866 | oral squamous cell carcinoma | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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DOID:0111459 | classic galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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DOID:684 | hepatocellular carcinoma | WB:WBGene00020557 | Caenorhabditis elegans | 172232 | aprt-1 |
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DOID:0050474 | Netherton syndrome | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:0050833 | orotic aciduria | WB:WBGene00020036 | Caenorhabditis elegans | 172008 | R12E2.11 |
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DOID:14735 | hereditary angioedema | WB:WBGene00044303 | Caenorhabditis elegans | 3564879 | hst-3.2 |
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DOID:2747 | glycogen storage disease | WB:WBGene00012020 | Caenorhabditis elegans | 180119 | gyg-2 |
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DOID:0060363 | glycerol kinase deficiency | WB:WBGene00020007 | Caenorhabditis elegans | 173747 | R11F4.1 |
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DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | WB:WBGene00015982 | Caenorhabditis elegans | 182795 | bgnt-1.4 |
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DOID:0050827 | rheumatic heart disease | WB:WBGene00001686 | Caenorhabditis elegans | 174578 | gpd-4 |
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DOID:10652 | Alzheimer's disease | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:0080562 | congenital disorder of glycosylation Ij | WB:WBGene00013362 | Caenorhabditis elegans | 190436 | algn-7 |
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DOID:9256 | colorectal cancer | WB:WBGene00001630 | Caenorhabditis elegans | 176736 | gly-5 |
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DOID:0112315 | brain small vessel disease 3 | WB:WBGene00008426 | Caenorhabditis elegans | 3565069 | D2045.9 |
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DOID:5212 | congenital disorder of glycosylation | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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DOID:2349 | arteriosclerosis | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:0060759 | immunodeficiency with hyper IgM type 5 | WB:WBGene00013241 | Caenorhabditis elegans | 176633 | ung-1 |
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DOID:2747 | glycogen storage disease | WB:WBGene00022199 | Caenorhabditis elegans | 180583 | pfk-1.1 |
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DOID:5199 | ureteral obstruction | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:5154 | borna disease | WB:WBGene00004051 | Caenorhabditis elegans | 177683 | parg-1 |
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DOID:0070254 | congenital disorder of glycosylation type IIb | WB:WBGene00008775 | Caenorhabditis elegans | 177998 | mogs-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