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:8947 | diabetic retinopathy | WB:WBGene00001683 | Caenorhabditis elegans | 174603 | gpd-1 |
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DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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DOID:2861 | congenital nonspherocytic hemolytic anemia | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:9884 | muscular dystrophy | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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DOID:3211 | lysosomal storage disease | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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DOID:0080855 | Parkinsonism | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:9279 | hyperhomocysteinemia | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:13276 | Mycoplasma pneumoniae pneumonia | WB:WBGene00016207 | Caenorhabditis elegans | 183002 | C29E4.10 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
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DOID:9352 | type 2 diabetes mellitus | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:3525 | middle cerebral artery infarction | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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DOID:0080411 | familial adenomatous polyposis 3 | WB:WBGene00011201 | Caenorhabditis elegans | 187770 | nth-1 |
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DOID:0060713 | autosomal recessive congenital ichthyosis 4B | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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DOID:1793 | pancreatic cancer | WB:WBGene00044303 | Caenorhabditis elegans | 3564879 | hst-3.2 |
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DOID:2741 | bilirubin metabolic disorder | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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DOID:0110444 | dilated cardiomyopathy 1X | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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DOID:6000 | congestive heart failure | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:0112250 | Gaucher's disease type IIIC | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:0110957 | Gaucher's disease type I | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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DOID:7998 | hyperthyroidism | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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DOID:206 | hereditary multiple exostoses | WB:WBGene00004361 | Caenorhabditis elegans | 176502 | rib-2 |
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DOID:12217 | Lewy body dementia | WB:WBGene00016340 | Caenorhabditis elegans | 183155 | gba-2 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007435 | Caenorhabditis elegans | 182392 | algn-6 |
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DOID:12783 | migraine without aura | WB:WBGene00011884 | Caenorhabditis elegans | 174423 | enol-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