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 | October 9, 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:13994 | cleidocranial dysplasia | MGI:99829 | Mus musculus (house mouse) | 12393 | Runx2 |
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DOID:14687 | diastrophic dysplasia | MGI:892977 | Mus musculus (house mouse) | 13521 | Slc26a2 |
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DOID:13628 | favism | MGI:105979 | Mus musculus (house mouse) | 14381 | G6pdx |
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DOID:0110467 | autosomal recessive nonsyndromic deafness 12 | MGI:1890219 | Mus musculus (house mouse) | 22295 | Cdh23 |
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DOID:3652 | Leigh disease | MGI:1343135 | Mus musculus (house mouse) | 17993 | Ndufs4 |
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DOID:0110910 | leukocyte adhesion deficiency 1 | MGI:96611 | Mus musculus (house mouse) | 16414 | Itgb2 |
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DOID:9352 | type 2 diabetes mellitus | MGI:1095438 | Mus musculus (house mouse) | 20526 | Slc2a2 |
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DOID:10588 | adrenoleukodystrophy | MGI:1349215 | Mus musculus (house mouse) | 11666 | Abcd1 |
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DOID:0090129 | carnitine palmitoyltransferase I deficiency | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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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:9352 | type 2 diabetes mellitus | MGI:104874 | Mus musculus (house mouse) | 11652 | Akt2 |
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DOID:0110726 | neuronal ceroid lipofuscinosis 2 | MGI:1336194 | Mus musculus (house mouse) | 12751 | Tpp1 |
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DOID:0060350 | adenine phosphoribosyltransferase deficiency | MGI:88061 | Mus musculus (house mouse) | 11821 | Aprt |
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DOID:0110927 | nemaline myopathy 3 | MGI:87902 | Mus musculus (house mouse) | 11459 | Acta1 |
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DOID:0110660 | congenital myasthenic syndrome 12 | MGI:95698 | Mus musculus (house mouse) | 14583 | Gfpt1 |
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DOID:0080418 | developmental and epileptic encephalopathy 54 | MGI:1858195 | Mus musculus (house mouse) | 51810 | Hnrnpu |
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DOID:0110915 | childhood hypophosphatasia | MGI:87983 | Mus musculus (house mouse) | 11647 | Alpl |
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DOID:0080056 | achondrogenesis type II | MGI:88452 | Mus musculus (house mouse) | 12824 | Col2a1 |
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DOID:12387 | nephrogenic diabetes insipidus | MGI:88123 | Mus musculus (house mouse) | 12000 | Avpr2 |
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DOID:0060929 | non-syndromic X-linked intellectual developmental disorder 111 | MGI:2679449 | Mus musculus (house mouse) | 245450 | Slitrk2 |
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DOID:3209 | junctional epidermolysis bullosa | MGI:99909 | Mus musculus (house mouse) | 16774 | Lama3 |
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DOID:3755 | antithrombin III deficiency | MGI:88095 | Mus musculus (house mouse) | 11905 | Serpinc1 |
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DOID:0050990 | episodic ataxia type 2 | MGI:109482 | Mus musculus (house mouse) | 12286 | Cacna1a |
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DOID:0090002 | Tietz syndrome | MGI:104554 | Mus musculus (house mouse) | 17342 | Mitf |
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DOID:9352 | type 2 diabetes mellitus | MGI:2153588 | Mus musculus (house mouse) | 140491 | Ppp1r3a |
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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 v4.1.0
Last updated: December 9, 2024