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:0050879 | fragile X-associated tremor/ataxia syndrome | HGNC:3775 | Homo sapiens (human) | 2332 | FMR1 |
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DOID:2945 | severe acute respiratory syndrome | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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DOID:0060173 | Timothy syndrome | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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DOID:10763 | hypertension | HGNC:4910 | Homo sapiens (human) | 3091 | HIF1A |
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DOID:9268 | glycine encephalopathy | HGNC:4313 | Homo sapiens (human) | 2731 | GLDC |
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DOID:9975 | cocaine dependence | RGD:61800 | Rattus norvegicus (Norway rat) | 29595 | Htr2a |
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DOID:2741 | bilirubin metabolic disorder | HGNC:53 | Homo sapiens (human) | 1244 | ABCC2 |
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DOID:2843 | long QT syndrome | HGNC:6251 | Homo sapiens (human) | 3757 | KCNH2 |
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DOID:2843 | long QT syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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DOID:10763 | hypertension | RGD:2965 | Rattus norvegicus (Norway rat) | 25589 | Kdr |
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DOID:0050559 | Fukuyama congenital muscular dystrophy | MGI:2179507 | Mus musculus (house mouse) | 246179 | Fktn |
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DOID:224 | transient cerebral ischemia | RGD:621159 | Rattus norvegicus (Norway rat) | 60582 | Il1rn |
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DOID:0060887 | ossification of the posterior longitudinal ligament of spine | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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DOID:0110861 | autosomal recessive polycystic kidney disease | MGI:2155808 | Mus musculus (house mouse) | 241035 | Pkhd1 |
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DOID:2349 | arteriosclerosis | HGNC:7176 | Homo sapiens (human) | 4318 | MMP9 |
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DOID:5325 | Roberts syndrome | HGNC:27230 | Homo sapiens (human) | 157570 | ESCO2 |
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DOID:4450 | renal cell carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:2841 | asthma | RGD:621700 | Rattus norvegicus (Norway rat) | 192155 | Sftpb |
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DOID:2841 | asthma | RGD:3665 | Rattus norvegicus (Norway rat) | 24773 | Sftpa1 |
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DOID:10763 | hypertension | RGD:3175 | Rattus norvegicus (Norway rat) | 24594 | Klk1b3 |
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DOID:10763 | hypertension | RGD:2969 | Rattus norvegicus (Norway rat) | 24523 | Klk1 |
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DOID:0060867 | macrocephaly-autism syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:10652 | Alzheimer's disease | RGD:621314 | Rattus norvegicus (Norway rat) | 63868 | Hspd1 |
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DOID:684 | hepatocellular carcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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DOID:10588 | adrenoleukodystrophy | HGNC:29567 | Homo sapiens (human) | 23205 | ACSBG1 |
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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