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:0060445 | congenital stromal corneal dystrophy | MGI:94872 | Mus musculus (house mouse) | 13179 | Dcn |
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DOID:10487 | Hirschsprung's disease | MGI:97902 | Mus musculus (house mouse) | 19713 | Ret |
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DOID:0110639 | congenital muscular dystrophy due to integrin alpha-7 deficiency | MGI:102700 | Mus musculus (house mouse) | 16404 | Itga7 |
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DOID:0060675 | catecholaminergic polymorphic ventricular tachycardia 1 | MGI:99685 | Mus musculus (house mouse) | 20191 | Ryr2 |
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DOID:1067 | open-angle glaucoma | MGI:1202864 | Mus musculus (house mouse) | 17926 | Myoc |
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DOID:0050579 | glycogen storage disease XV | MGI:1351614 | Mus musculus (house mouse) | 27357 | Gyg1 |
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DOID:0090019 | sitosterolemia | MGI:1914720 | Mus musculus (house mouse) | 67470 | Abcg8 |
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DOID:0110969 | brachydactyly type B1 | MGI:1347521 | Mus musculus (house mouse) | 26564 | Ror2 |
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DOID:10487 | Hirschsprung's disease | MGI:107430 | Mus musculus (house mouse) | 14573 | Gdnf |
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DOID:0110657 | congenital myasthenic syndrome 8 | MGI:87961 | Mus musculus (house mouse) | 11603 | Agrn |
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DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | MGI:895149 | Mus musculus (house mouse) | 11370 | Acadvl |
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DOID:0050445 | X-linked dominant hypophosphatemic rickets | MGI:107489 | Mus musculus (house mouse) | 18675 | Phex |
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DOID:2842 | Jervell-Lange Nielsen syndrome | MGI:108083 | Mus musculus (house mouse) | 16535 | Kcnq1 |
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DOID:12259 | hemophilia B | MGI:88384 | Mus musculus (house mouse) | 14071 | F9 |
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DOID:13482 | Proteus syndrome | MGI:87986 | Mus musculus (house mouse) | 11651 | Akt1 |
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DOID:206 | hereditary multiple exostoses | MGI:894663 | Mus musculus (house mouse) | 14042 | Ext1 |
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DOID:988 | mitral valve prolapse | MGI:2685011 | Mus musculus (house mouse) | 233651 | Dchs1 |
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DOID:0110334 | osteogenesis imperfecta type 1 | MGI:88467 | Mus musculus (house mouse) | 12842 | Col1a1 |
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DOID:12365 | malaria | MGI:96392 | Mus musculus (house mouse) | 15894 | Icam1 |
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DOID:0110544 | autosomal dominant nonsyndromic deafness 12 | MGI:109575 | Mus musculus (house mouse) | 21683 | Tecta |
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DOID:2736 | Hajdu-Cheney syndrome | MGI:97364 | Mus musculus (house mouse) | 18129 | Notch2 |
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DOID:14755 | argininosuccinic aciduria | MGI:88084 | Mus musculus (house mouse) | 109900 | Asl |
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DOID:9119 | acute myeloid leukemia | MGI:2684063 | Mus musculus (house mouse) | 228790 | Asxl1 |
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DOID:5419 | schizophrenia | MGI:1891700 | Mus musculus (house mouse) | 59287 | Ncstn |
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DOID:0080196 | mandibulofacial dysostosis, Guion-Almeida type | MGI:1336880 | Mus musculus (house mouse) | 20624 | Eftud2 |
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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