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:12801 | mucopolysaccharidosis III | MGI:1350341 | Mus musculus (house mouse) | 27029 | Sgsh |
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DOID:0060768 | Smith-Magenis syndrome | MGI:103291 | Mus musculus (house mouse) | 19377 | Rai1 |
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DOID:0080312 | neurodevelopmental disorder with midbrain and hindbrain malformations | MGI:103264 | Mus musculus (house mouse) | 16800 | Arhgef2 |
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DOID:3347 | osteosarcoma | MGI:98834 | Mus musculus (house mouse) | 22059 | Trp53 |
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DOID:0110475 | autosomal recessive nonsyndromic deafness 1A | MGI:107588 | Mus musculus (house mouse) | 14623 | Gjb6 |
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DOID:0111182 | familial hemiplegic migraine 2 | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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DOID:1060 | Hartnup disease | MGI:1921588 | Mus musculus (house mouse) | 74338 | Slc6a19 |
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DOID:0080450 | developmental and epileptic encephalopathy 17 | MGI:95775 | Mus musculus (house mouse) | 14681 | Gnao1 |
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DOID:898 | autosomal dominant polycystic kidney disease | MGI:1099818 | Mus musculus (house mouse) | 18764 | Pkd2 |
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DOID:14330 | Parkinson's disease | MGI:1342774 | Mus musculus (house mouse) | 19017 | Ppargc1a |
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DOID:0060485 | Mowat-Wilson syndrome | MGI:1344407 | Mus musculus (house mouse) | 24136 | Zeb2 |
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DOID:3827 | congenital diaphragmatic hernia | MGI:2670972 | Mus musculus (house mouse) | 329872 | Frem1 |
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DOID:14693 | Clouston syndrome | MGI:107588 | Mus musculus (house mouse) | 14623 | Gjb6 |
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DOID:3413 | alpha-mannosidosis | MGI:107286 | Mus musculus (house mouse) | 17159 | Man2b1 |
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DOID:0111028 | hemochromatosis type 4 | MGI:1315204 | Mus musculus (house mouse) | 53945 | Slc40a1 |
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DOID:10652 | Alzheimer's disease | MGI:96828 | Mus musculus (house mouse) | 16971 | Lrp1 |
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DOID:0070069 | autosomal dominant intellectual developmental disorder 39 | MGI:1100511 | Mus musculus (house mouse) | 17933 | Myt1l |
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DOID:2734 | keratosis follicularis | MGI:88110 | Mus musculus (house mouse) | 11938 | Atp2a2 |
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DOID:2217 | Bernard-Soulier syndrome | MGI:1333744 | Mus musculus (house mouse) | 14723 | Gp1ba |
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DOID:3210 | Pelizaeus-Merzbacher disease | MGI:97623 | Mus musculus (house mouse) | 18823 | Plp1 |
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DOID:0060316 | orofaciodigital syndrome I | MGI:1350328 | Mus musculus (house mouse) | 237222 | Ofd1 |
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DOID:0050989 | episodic ataxia type 1 | MGI:96654 | Mus musculus (house mouse) | 16485 | Kcna1 |
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DOID:13544 | low tension glaucoma | MGI:98351 | Mus musculus (house mouse) | 20655 | Sod1 |
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DOID:0110144 | Bartter disease type 3 | MGI:1930643 | Mus musculus (house mouse) | 56365 | Clcnkb |
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DOID:0050886 | Troyer syndrome | MGI:2139806 | Mus musculus (house mouse) | 229285 | Spart |
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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
This work is licensed under Creative Commons Attribution 4.0 International
GlyCosmos Portal v4.1.1
Last updated: February 17, 2025