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:14330 | Parkinson's disease | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:0110663 | congenital myasthenic syndrome 1A | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:2316 | brain ischemia | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:8893 | psoriasis | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:9952 | acute lymphoblastic leukemia | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:1574 | alcohol use disorder | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:14067 | Plasmodium falciparum malaria | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:0070526 | PLACK syndrome | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:7148 | rheumatoid arthritis | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:12894 | Sjogren's syndrome | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:10652 | Alzheimer's disease | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:9182 | pemphigus | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:767 | muscular atrophy | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:10763 | hypertension | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:9074 | systemic lupus erythematosus | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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DOID:1936 | atherosclerosis | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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DOID:12466 | secondary hyperparathyroidism | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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DOID:5844 | myocardial infarction | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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DOID:13543 | hyperparathyroidism | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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DOID:12678 | hypercalcemia | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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DOID:0050700 | cardiomyopathy | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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DOID:0111322 | idiopathic generalized epilepsy 8 | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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DOID:0090107 | autosomal dominant hypocalcemia 1 | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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DOID:0060700 | familial hypocalciuric hypercalcemia 1 | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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DOID:6432 | pulmonary hypertension | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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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