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 | MGI:96573 | Mus musculus (house mouse) | 16334 | Ins2 |
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DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | MGI:2447586 | Mus musculus (house mouse) | 243853 | Fkrp |
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DOID:9352 | type 2 diabetes mellitus | MGI:104874 | Mus musculus (house mouse) | 11652 | Akt2 |
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DOID:8584 | Burkitt lymphoma | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | MGI:2445096 | Mus musculus (house mouse) | 209692 | Dhtkd1 |
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DOID:1919 | Lesch-Nyhan syndrome | MGI:96217 | Mus musculus (house mouse) | 15452 | Hprt1 |
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DOID:0060233 | cardiofaciocutaneous syndrome | MGI:88190 | Mus musculus (house mouse) | 109880 | Braf |
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DOID:13317 | hyperinsulinemic hypoglycemia | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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DOID:0050570 | congenital disorder of glycosylation type I | MGI:97075 | Mus musculus (house mouse) | 110119 | Mpi |
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DOID:14504 | Niemann-Pick disease | MGI:1097712 | Mus musculus (house mouse) | 18145 | Npc1 |
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DOID:13482 | Proteus syndrome | MGI:87986 | Mus musculus (house mouse) | 11651 | Akt1 |
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DOID:0070253 | congenital disorder of glycosylation type IIa | MGI:2384966 | Mus musculus (house mouse) | 217664 | Mgat2 |
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DOID:9970 | obesity | MGI:104663 | Mus musculus (house mouse) | 16846 | Lep |
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DOID:10587 | Krabbe disease | MGI:95636 | Mus musculus (house mouse) | 14420 | Galc |
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DOID:9884 | muscular dystrophy | MGI:2447586 | Mus musculus (house mouse) | 243853 | Fkrp |
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DOID:0080201 | Peters plus syndrome | MGI:2685903 | Mus musculus (house mouse) | 381694 | B3glct |
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DOID:0050570 | congenital disorder of glycosylation type I | MGI:1859214 | Mus musculus (house mouse) | 54128 | Pmm2 |
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DOID:12803 | Sly syndrome | MGI:95872 | Mus musculus (house mouse) | 110006 | Gusb |
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DOID:2749 | glycogen storage disease Ia | MGI:95607 | Mus musculus (house mouse) | 14377 | G6pc1 |
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DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | MGI:1342270 | Mus musculus (house mouse) | 16795 | Large1 |
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DOID:0050663 | Bethlem myopathy | MGI:88459 | Mus musculus (house mouse) | 12833 | Col6a1 |
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DOID:0110276 | autosomal recessive limb-girdle muscular dystrophy type 2B | MGI:1349385 | Mus musculus (house mouse) | 26903 | Dysf |
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DOID:3413 | alpha-mannosidosis | MGI:107286 | Mus musculus (house mouse) | 17159 | Man2b1 |
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DOID:2754 | glycogen storage disease VI | MGI:97829 | Mus musculus (house mouse) | 110095 | Pygl |
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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