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 | July 29, 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:8466 | retinal degeneration | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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DOID:0050852 | limb ischemia | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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DOID:11984 | hypertrophic cardiomyopathy | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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DOID:12930 | dilated cardiomyopathy | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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DOID:5844 | myocardial infarction | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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DOID:7998 | hyperthyroidism | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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DOID:6000 | congestive heart failure | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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DOID:1459 | hypothyroidism | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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DOID:2256 | osteochondrodysplasia | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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DOID:0080046 | Stickler syndrome | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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DOID:0070298 | multiple epiphyseal dysplasia 2 | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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DOID:11446 | sciatic neuropathy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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DOID:11832 | visual epilepsy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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DOID:552 | pneumonia | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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DOID:2913 | acute pancreatitis | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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DOID:9352 | type 2 diabetes mellitus | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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DOID:9870 | galactosemia | HGNC:24063 | Homo sapiens (human) | 130589 | GALM |
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DOID:14330 | Parkinson's disease | HGNC:256 | Homo sapiens (human) | 131 | ADH7 |
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DOID:10763 | hypertension | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:1574 | alcohol use disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:12306 | vitiligo | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:1612 | breast cancer | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:11612 | polycystic ovary syndrome | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:0060041 | autism spectrum disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:4450 | renal cell carcinoma | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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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 v4.0.0
Last updated: August 19, 2024