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:0090132 | complex cortical dysplasia with other brain malformations 7 | MGI:1920960 | Mus musculus (house mouse) | 73710 | Tubb2b |
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DOID:0110194 | Charcot-Marie-Tooth disease type 4B3 | MGI:1925230 | Mus musculus (house mouse) | 77980 | Sbf1 |
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DOID:0050144 | Kartagener syndrome | MGI:1100864 | Mus musculus (house mouse) | 13411 | Dnah11 |
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DOID:0110957 | Gaucher's disease type I | MGI:95665 | Mus musculus (house mouse) | 14466 | Gba1 |
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DOID:0111020 | cone-rod dystrophy 9 | MGI:105376 | Mus musculus (house mouse) | 11502 | Adam9 |
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DOID:12134 | factor VIII deficiency | MGI:88383 | Mus musculus (house mouse) | 14069 | F8 |
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DOID:10588 | adrenoleukodystrophy | MGI:1349215 | Mus musculus (house mouse) | 11666 | Abcd1 |
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DOID:0060684 | autosomal dominant nocturnal frontal lobe epilepsy 3 | MGI:87891 | Mus musculus (house mouse) | 11444 | Chrnb2 |
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DOID:0080119 | mitochondrial DNA depletion syndrome 1 | MGI:1920212 | Mus musculus (house mouse) | 72962 | Tymp |
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DOID:0090071 | hypogonadotropic hypogonadism 11 with or without anosmia | MGI:892968 | Mus musculus (house mouse) | 21338 | Tacr3 |
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DOID:0110266 | cataract 9 multiple types | MGI:88515 | Mus musculus (house mouse) | 12954 | Cryaa |
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DOID:0110555 | autosomal dominant nonsyndromic deafness 25 | MGI:3039629 | Mus musculus (house mouse) | 216227 | Slc17a8 |
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DOID:0090118 | congenital amegakaryocytic thrombocytopenia | MGI:97076 | Mus musculus (house mouse) | 17480 | Mpl |
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DOID:12259 | hemophilia B | MGI:88384 | Mus musculus (house mouse) | 14071 | F9 |
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DOID:1270 | hereditary hemorrhagic telangiectasia | MGI:1338946 | Mus musculus (house mouse) | 11482 | Acvrl1 |
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DOID:3209 | junctional epidermolysis bullosa | MGI:88450 | Mus musculus (house mouse) | 12821 | Col17a1 |
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DOID:0050535 | exudative vitreoretinopathy | MGI:108520 | Mus musculus (house mouse) | 14366 | Fzd4 |
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DOID:1928 | Williams-Beuren syndrome | MGI:104572 | Mus musculus (house mouse) | 16885 | Limk1 |
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DOID:0110033 | autosomal recessive Alport syndrome | MGI:104688 | Mus musculus (house mouse) | 12828 | Col4a3 |
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DOID:2752 | glycogen storage disease II | MGI:95609 | Mus musculus (house mouse) | 14387 | Gaa |
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DOID:0110867 | congenital stationary night blindness 1C | MGI:1330305 | Mus musculus (house mouse) | 17364 | Trpm1 |
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DOID:0050800 | cerebral creatine deficiency syndrome 1 | MGI:2147834 | Mus musculus (house mouse) | 102857 | Slc6a8 |
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DOID:0110678 | congenital myasthenic syndrome 4A | MGI:87894 | Mus musculus (house mouse) | 11448 | Chrne |
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DOID:9884 | muscular dystrophy | MGI:2447586 | Mus musculus (house mouse) | 243853 | Fkrp |
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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
This work is licensed under Creative Commons Attribution 4.0 International
GlyCosmos Portal v4.1.1
Last updated: February 17, 2025