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:13580 | cholestasis | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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DOID:9352 | type 2 diabetes mellitus | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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DOID:3908 | lung non-small cell carcinoma | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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DOID:14330 | Parkinson's disease | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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DOID:9970 | obesity | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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DOID:0111230 | congenital muscular dystrophy-dystroglycanopathy type A11 | MGI:2145517 | Mus musculus (house mouse) | 97884 | B3galnt2 |
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DOID:3534 | Lafora disease | MGI:2145264 | Mus musculus (house mouse) | 105193 | Nhlrc1 |
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DOID:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | MGI:2143424 | Mus musculus (house mouse) | 215494 | Pomgnt2 |
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DOID:0112382 | muscular dystrophy-dystroglycanopathy type C8 | MGI:2143424 | Mus musculus (house mouse) | 215494 | Pomgnt2 |
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DOID:1793 | pancreatic cancer | MGI:2143261 | Mus musculus (house mouse) | 333424 | A4gnt |
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DOID:0080567 | congenital disorder of glycosylation Ip | MGI:2142632 | Mus musculus (house mouse) | 207958 | Alg11 |
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DOID:0050570 | congenital disorder of glycosylation type I | MGI:2141959 | Mus musculus (house mouse) | 381903 | Alg8 |
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DOID:0050770 | polycystic liver disease | MGI:2141959 | Mus musculus (house mouse) | 381903 | Alg8 |
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DOID:0080560 | congenital disorder of glycosylation Ih | MGI:2141959 | Mus musculus (house mouse) | 381903 | Alg8 |
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DOID:0060227 | Adams-Oliver syndrome | MGI:2141669 | Mus musculus (house mouse) | 101351 | Eogt |
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DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | MGI:2140364 | Mus musculus (house mouse) | 100206 | Adprs |
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DOID:0090139 | cortisone reductase deficiency | MGI:2140356 | Mus musculus (house mouse) | 100198 | H6pd |
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DOID:0090141 | cortisone reductase deficiency 1 | MGI:2140356 | Mus musculus (house mouse) | 100198 | H6pd |
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DOID:2377 | multiple sclerosis | MGI:2140356 | Mus musculus (house mouse) | 100198 | H6pd |
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DOID:0060230 | basal ganglia calcification | MGI:2140300 | Mus musculus (house mouse) | 329828 | Myorg |
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DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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DOID:0050453 | lissencephaly | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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DOID:0112374 | muscular dystrophy-dystroglycanopathy | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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DOID:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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DOID:0050560 | Walker-Warburg syndrome | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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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