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 | July 29, 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:9266 | cystinuria | FB:FBgn0002569 | Drosophila melanogaster (fruit fly) | 35825 | Mal-A2 |
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DOID:9352 | type 2 diabetes mellitus | MGI:1915304 | Mus musculus (house mouse) | 68054 | Serpina12 |
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DOID:0112182 | mismatch repair cancer syndrome | MGI:98834 | Mus musculus (house mouse) | 22059 | Trp53 |
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DOID:11151 | cholecystolithiasis | FB:FBgn0032684 | Drosophila melanogaster (fruit fly) | 35105 | Ugt301D1 |
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DOID:12554 | hemolytic-uremic syndrome | MGI:1913493 | Mus musculus (house mouse) | 59048 | C1galt1c1 |
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DOID:1495 | cystic echinococcosis | RGD:3870 | Rattus norvegicus (Norway rat) | 29260 | Tlr4 |
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DOID:0080081 | nonsyndromic congenital nail disorder 3 | HGNC:9060 | Homo sapiens (human) | 5333 | PLCD1 |
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DOID:1123 | spondyloarthropathy | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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DOID:1824 | status epilepticus | SGD:S000004954 | Saccharomyces cerevisiae S288C | 855723 | IDP3 |
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DOID:2297 | leptospirosis | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:0060224 | atrial fibrillation | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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DOID:0060340 | ciliopathy | MGI:1927136 | Mus musculus (house mouse) | 56297 | Arl6 |
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DOID:114 | heart disease | MGI:1861437 | Mus musculus (house mouse) | 56637 | Gsk3b |
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DOID:1062 | Fanconi syndrome | HGNC:2518 | Homo sapiens (human) | 1497 | CTNS |
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DOID:7998 | hyperthyroidism | Xenbase:XB-GENE-998849 | Xenopus tropicalis (tropical clawed frog) | 100489505 | ugt1a1 |
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DOID:684 | hepatocellular carcinoma | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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DOID:0050156 | idiopathic pulmonary fibrosis | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:10763 | hypertension | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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DOID:1574 | alcohol use disorder | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:12120 | pulmonary alveolar proteinosis | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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DOID:4989 | pancreatitis | RGD:61800 | Rattus norvegicus (Norway rat) | 29595 | Htr2a |
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DOID:5212 | congenital disorder of glycosylation | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
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DOID:12554 | hemolytic-uremic syndrome | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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DOID:9884 | muscular dystrophy | MGI:2447586 | Mus musculus (house mouse) | 243853 | Fkrp |
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DOID:0081210 | autosomal recessive intellectual developmental disorder 46 | Xenbase:XB-GENE-955052 | Xenopus tropicalis (tropical clawed frog) | 496577 | ndst1 |
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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 v4.0.0
Last updated: August 19, 2024