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:0080326 | familial hypertrophic cardiomyopathy | MGI:1925847 | Mus musculus (house mouse) | 225288 | Fhod3 |
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DOID:9155 | mucocutaneous leishmaniasis | RGD:3020 | Rattus norvegicus (Norway rat) | 25008 | Lta |
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DOID:12134 | factor VIII deficiency | RGD:3342 | Rattus norvegicus (Norway rat) | 25692 | Plat |
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DOID:576 | proteinuria | MGI:104849 | Mus musculus (house mouse) | 13137 | Cd55b |
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DOID:1612 | breast cancer | Xenbase:XB-GENE-5793241 | Xenopus tropicalis (tropical clawed frog) | 100135191 | ugt1a6 |
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DOID:14504 | Niemann-Pick disease | SGD:S000002860 | Saccharomyces cerevisiae S288C | 852063 | PPN1 |
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DOID:1596 | depressive disorder | FB:FBgn0000038 | Drosophila melanogaster (fruit fly) | 38545 | nAChRbeta1 |
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DOID:2476 | hereditary spastic paraplegia | HGNC:10469 | Homo sapiens (human) | 10313 | RTN3 |
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DOID:10591 | pre-eclampsia | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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DOID:9970 | obesity | MGI:2443847 | Mus musculus (house mouse) | 237979 | Sdk2 |
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DOID:0050741 | alcohol dependence | RGD:61966 | Rattus norvegicus (Norway rat) | 29709 | Gabrg2 |
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DOID:10923 | sickle cell anemia | MGI:104887 | Mus musculus (house mouse) | 14775 | Gpx1 |
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DOID:1407 | anterior uveitis | MGI:95896 | Mus musculus (house mouse) | 14964 | H2-D1 |
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DOID:0110393 | retinitis pigmentosa 66 | MGI:97878 | Mus musculus (house mouse) | 19661 | Rbp3 |
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DOID:8924 | autoimmune thrombocytopenic purpura | MGI:97610 | Mus musculus (house mouse) | 18791 | Plat |
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DOID:9970 | obesity | HGNC:6125 | Homo sapiens (human) | 3667 | IRS1 |
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DOID:0080422 | Dravet syndrome | MGI:1345149 | Mus musculus (house mouse) | 24046 | Scn11a |
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DOID:4440 | seminoma | WB:WBGene00000898 | Caenorhabditis elegans | 175410 | daf-2 |
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DOID:8923 | skin melanoma | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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DOID:2476 | hereditary spastic paraplegia | WB:WBGene00009164 | Caenorhabditis elegans | 172833 | hrdl-1 |
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DOID:3211 | lysosomal storage disease | MGI:1924193 | Mus musculus (house mouse) | 76943 | Psapl1 |
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DOID:10584 | retinitis pigmentosa | HGNC:3642 | Homo sapiens (human) | 2232 | FDXR |
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DOID:0070118 | Meckel syndrome 4 | MGI:2384917 | Mus musculus (house mouse) | 216274 | Cep290 |
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DOID:0050978 | spinocerebellar ataxia type 29 | MGI:96623 | Mus musculus (house mouse) | 16438 | Itpr1 |
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DOID:162 | cancer | HGNC:2433 | Homo sapiens (human) | 1436 | CSF1R |
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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