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:2018 | hyperinsulinism | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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DOID:0050633 | ocular albinism 1 | MGI:107193 | Mus musculus (house mouse) | 18241 | Gpr143 |
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DOID:1574 | alcohol use disorder | FB:FBgn0010329 | Drosophila melanogaster (fruit fly) | 31718 | Tbh |
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DOID:0110152 | Charcot-Marie-Tooth disease type 1B | MGI:103177 | Mus musculus (house mouse) | 17528 | Mpz |
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DOID:9352 | type 2 diabetes mellitus | MGI:109334 | Mus musculus (house mouse) | 384783 | Irs2 |
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DOID:10763 | hypertension | HGNC:3176 | Homo sapiens (human) | 1906 | EDN1 |
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DOID:11247 | disseminated intravascular coagulation | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:10283 | prostate cancer | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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DOID:9074 | systemic lupus erythematosus | MGI:88228 | Mus musculus (house mouse) | 12268 | C4b |
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DOID:12716 | newborn respiratory distress syndrome | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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DOID:12716 | newborn respiratory distress syndrome | HGNC:10801 | Homo sapiens (human) | 6439 | SFTPB |
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DOID:0050545 | visceral heterotaxy | HGNC:33983 | Homo sapiens (human) | 653275 | CFC1B |
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DOID:0050948 | autosomal dominant hypophosphatemic rickets | HGNC:3680 | Homo sapiens (human) | 8074 | FGF23 |
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DOID:14323 | Marfan syndrome | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
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DOID:0110313 | hypertrophic cardiomyopathy 7 | MGI:98783 | Mus musculus (house mouse) | 21954 | Tnni3 |
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DOID:14330 | Parkinson's disease | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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DOID:2921 | glomerulonephritis | HGNC:6156 | Homo sapiens (human) | 3690 | ITGB3 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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DOID:2842 | Jervell-Lange Nielsen syndrome | MGI:96673 | Mus musculus (house mouse) | 16509 | Kcne1 |
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DOID:2236 | congenital afibrinogenemia | HGNC:3694 | Homo sapiens (human) | 2266 | FGG |
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DOID:10763 | hypertension | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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DOID:0110679 | congenital myasthenic syndrome 4C | MGI:87894 | Mus musculus (house mouse) | 11448 | Chrne |
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DOID:10763 | hypertension | RGD:2071 | Rattus norvegicus (Norway rat) | 81638 | Agtr1b |
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DOID:4450 | renal cell carcinoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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DOID:9074 | systemic lupus erythematosus | MGI:95499 | Mus musculus (house mouse) | 14130 | Fcgr2b |
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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