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:17142 | Homo sapiens (human) | 10133 | OPTN |
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DOID:0081294 | neuronal intranuclear inclusion disease | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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DOID:13544 | low tension glaucoma | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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DOID:1686 | glaucoma | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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DOID:12858 | Huntington's disease | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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DOID:13948 | bladder neck obstruction | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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DOID:1067 | open-angle glaucoma | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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DOID:5408 | Paget's disease of bone | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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DOID:1070 | primary open angle glaucoma | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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DOID:576 | proteinuria | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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DOID:0070033 | autosomal dominant intellectual developmental disorder 3 | HGNC:1754 | Homo sapiens (human) | 1013 | CDH15 |
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DOID:0050888 | syndromic intellectual disability | HGNC:20367 | Homo sapiens (human) | 10129 | FRY |
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DOID:0111180 | French Canadian Leigh disease | HGNC:15714 | Homo sapiens (human) | 10128 | LRPPRC |
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DOID:3652 | Leigh disease | HGNC:15714 | Homo sapiens (human) | 10128 | LRPPRC |
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DOID:14250 | Down syndrome | HGNC:167 | Homo sapiens (human) | 10121 | ACTR1A |
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DOID:219 | colon cancer | HGNC:167 | Homo sapiens (human) | 10121 | ACTR1A |
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DOID:2349 | arteriosclerosis | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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DOID:4247 | coronary restenosis | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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DOID:1612 | breast cancer | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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DOID:10283 | prostate cancer | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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DOID:2871 | endometrial carcinoma | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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DOID:2394 | ovarian cancer | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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DOID:303 | substance-related disorder | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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DOID:3459 | breast carcinoma | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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DOID:3908 | lung non-small cell carcinoma | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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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