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:0080634 | nanophthalmos | HGNC:1181 | Homo sapiens (human) | 745 | MYRF |
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DOID:5614 | eye disease | HGNC:1181 | Homo sapiens (human) | 745 | MYRF |
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DOID:9834 | hyperopia | HGNC:1181 | Homo sapiens (human) | 745 | MYRF |
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DOID:1312 | focal segmental glomerulosclerosis | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:2217 | Bernard-Soulier syndrome | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:783 | end stage renal disease | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:0060573 | von Willebrand's disease 1 | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:0060224 | atrial fibrillation | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:10159 | osteonecrosis | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:0060574 | von Willebrand's disease 2 | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:5419 | schizophrenia | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:4450 | renal cell carcinoma | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:6432 | pulmonary hypertension | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:3407 | carotid artery disease | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:224 | transient cerebral ischemia | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:8947 | diabetic retinopathy | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:5844 | myocardial infarction | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:10763 | hypertension | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:418 | systemic scleroderma | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:2224 | essential thrombocythemia | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:9970 | obesity | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:12531 | von Willebrand's disease | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:13241 | Behcet's disease | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:13809 | familial combined hyperlipidemia | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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DOID:9744 | type 1 diabetes mellitus | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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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