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:14004 | thoracic aortic aneurysm | MGI:87905 | Mus musculus (house mouse) | 11464 | Actc1 |
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DOID:0110110 | atrial heart septal defect 5 | MGI:87905 | Mus musculus (house mouse) | 11464 | Actc1 |
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DOID:13250 | diarrhea | RGD:620623 | Rattus norvegicus (Norway rat) | 114629 | Slc26a3 |
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DOID:0060296 | congenital secretory chloride diarrhea 1 | RGD:620623 | Rattus norvegicus (Norway rat) | 114629 | Slc26a3 |
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DOID:2349 | arteriosclerosis | RGD:620298 | Rattus norvegicus (Norway rat) | 114628 | Abcg5 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | RGD:620298 | Rattus norvegicus (Norway rat) | 114628 | Abcg5 |
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DOID:9970 | obesity | RGD:620298 | Rattus norvegicus (Norway rat) | 114628 | Abcg5 |
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DOID:0090019 | sitosterolemia | RGD:620298 | Rattus norvegicus (Norway rat) | 114628 | Abcg5 |
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DOID:13580 | cholestasis | RGD:620298 | Rattus norvegicus (Norway rat) | 114628 | Abcg5 |
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DOID:0050328 | congenital hypothyroidism | RGD:69267 | Rattus norvegicus (Norway rat) | 114613 | Slc5a5 |
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DOID:0050718 | vitamin metabolic disorder | RGD:69267 | Rattus norvegicus (Norway rat) | 114613 | Slc5a5 |
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DOID:0112185 | thyroid dyshormonogenesis 1 | RGD:69267 | Rattus norvegicus (Norway rat) | 114613 | Slc5a5 |
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DOID:1588 | thrombocytopenia | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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DOID:0081112 | Baraitser-Winter syndrome 1 | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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DOID:0110550 | autosomal dominant nonsyndromic deafness 20 | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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DOID:13099 | Moyamoya disease | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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DOID:3328 | temporal lobe epilepsy | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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DOID:423 | myopathy | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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DOID:3191 | nemaline myopathy | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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DOID:14004 | thoracic aortic aneurysm | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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DOID:422 | congenital structural myopathy | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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DOID:11984 | hypertrophic cardiomyopathy | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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DOID:10881 | hand, foot and mouth disease | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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DOID:10486 | intestinal atresia | MGI:87904 | Mus musculus (house mouse) | 11461 | Actb |
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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