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:206 | hereditary multiple exostoses | FB:FBgn0027535 | Drosophila melanogaster (fruit fly) | 37198 | botv | CG15110 |
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DOID:5419 | schizophrenia | FB:FBgn0001083 | Drosophila melanogaster (fruit fly) | 32162 | fw | CG1500 |
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DOID:0080600 | COVID-19 | FB:FBgn0001083 | Drosophila melanogaster (fruit fly) | 32162 | fw | CG1500 |
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DOID:14250 | Down syndrome | FB:FBgn0027791 | Drosophila melanogaster (fruit fly) | 31098 | O-fut2 | CG14789 |
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DOID:2377 | multiple sclerosis | FB:FBgn0039625 | Drosophila melanogaster (fruit fly) | 43425 | beta4GalNAcTB | CG14517 |
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DOID:2377 | multiple sclerosis | FB:FBgn0039625 | Drosophila melanogaster (fruit fly) | 43425 | β4GalNAcTB | CG14517 |
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DOID:3211 | lysosomal storage disease | FB:FBgn0041630 | Drosophila melanogaster (fruit fly) | 38528 | Hexo1 | CG1318 |
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DOID:3323 | Sandhoff disease | FB:FBgn0041630 | Drosophila melanogaster (fruit fly) | 38528 | Hexo1 | CG1318 |
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DOID:12377 | spinal muscular atrophy | FB:FBgn0041630 | Drosophila melanogaster (fruit fly) | 38528 | Hexo1 | CG1318 |
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DOID:3320 | Tay-Sachs disease | FB:FBgn0041630 | Drosophila melanogaster (fruit fly) | 38528 | Hexo1 | CG1318 |
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DOID:0080561 | congenital disorder of glycosylation Ii | FB:FBgn0035401 | Drosophila melanogaster (fruit fly) | 38374 | Alg2 | CG1291 |
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DOID:0110669 | congenital myasthenic syndrome 14 | FB:FBgn0035401 | Drosophila melanogaster (fruit fly) | 38374 | Alg2 | CG1291 |
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DOID:0060256 | Dowling-Degos disease | FB:FBgn0033901 | Drosophila melanogaster (fruit fly) | 36564 | O-fut1 | CG12366 |
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DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | FB:FBgn0086368 | Drosophila melanogaster (fruit fly) | 31024 | tw | CG12311 |
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DOID:9884 | muscular dystrophy | FB:FBgn0086368 | Drosophila melanogaster (fruit fly) | 31024 | tw | CG12311 |
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DOID:0050560 | Walker-Warburg syndrome | FB:FBgn0086368 | Drosophila melanogaster (fruit fly) | 31024 | tw | CG12311 |
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DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | FB:FBgn0086368 | Drosophila melanogaster (fruit fly) | 31024 | tw | CG12311 |
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DOID:0112374 | muscular dystrophy-dystroglycanopathy | FB:FBgn0086368 | Drosophila melanogaster (fruit fly) | 31024 | tw | CG12311 |
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DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | FB:FBgn0086368 | Drosophila melanogaster (fruit fly) | 31024 | tw | CG12311 |
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DOID:0050453 | lissencephaly | FB:FBgn0086368 | Drosophila melanogaster (fruit fly) | 31024 | tw | CG12311 |
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DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | FB:FBgn0086368 | Drosophila melanogaster (fruit fly) | 31024 | tw | CG12311 |
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DOID:9970 | obesity | FB:FBgn0015622 | Drosophila melanogaster (fruit fly) | 44643 | Cnx99A | CG11958 |
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DOID:0081097 | Rafiq syndrome | FB:FBgn0039634 | Drosophila melanogaster (fruit fly) | 43436 | α-Man-Ib | CG11874 |
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DOID:0081097 | Rafiq syndrome | FB:FBgn0039634 | Drosophila melanogaster (fruit fly) | 43436 | alpha-Man-Ib | CG11874 |
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DOID:0080564 | congenital disorder of glycosylation Il | FB:FBgn0039293 | Drosophila melanogaster (fruit fly) | 43031 | Alg9 | CG11851 |
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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