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:1574 | alcohol use disorder | HGNC:24124 | Homo sapiens (human) | 86 | ACTL6A |
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DOID:10486 | intestinal atresia | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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DOID:13832 | patent ductus arteriosus | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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DOID:0081113 | Baraitser-Winter syndrome 2 | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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DOID:0081112 | Baraitser-Winter syndrome 1 | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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DOID:0110550 | autosomal dominant nonsyndromic deafness 20 | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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DOID:14004 | thoracic aortic aneurysm | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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DOID:13099 | Moyamoya disease | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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DOID:13099 | Moyamoya disease | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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DOID:0110317 | hypertrophic cardiomyopathy 11 | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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DOID:14004 | thoracic aortic aneurysm | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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DOID:0110456 | dilated cardiomyopathy 1R | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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DOID:12930 | dilated cardiomyopathy | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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DOID:0110110 | atrial heart septal defect 5 | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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DOID:10763 | hypertension | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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DOID:0110550 | autosomal dominant nonsyndromic deafness 20 | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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DOID:0081112 | Baraitser-Winter syndrome 1 | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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DOID:10486 | intestinal atresia | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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DOID:3191 | nemaline myopathy | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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DOID:13832 | patent ductus arteriosus | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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DOID:0081112 | Baraitser-Winter syndrome 1 | HGNC:17780 | Homo sapiens (human) | 345651 | ACTBL2 |
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DOID:13832 | patent ductus arteriosus | HGNC:17780 | Homo sapiens (human) | 345651 | ACTBL2 |
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DOID:14004 | thoracic aortic aneurysm | HGNC:17780 | Homo sapiens (human) | 345651 | ACTBL2 |
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DOID:10486 | intestinal atresia | HGNC:17780 | Homo sapiens (human) | 345651 | ACTBL2 |
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DOID:13099 | Moyamoya disease | HGNC:17780 | Homo sapiens (human) | 345651 | ACTBL2 |
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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