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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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MIRAGE
Alliance of Genome Resources
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 |
|---|---|
| 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 |
|---|---|---|---|---|---|---|---|---|
| DOID:0060019 | coronin-1A deficiency | HGNC:2252 | Homo sapiens (human) | 11151 | CORO1A |
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| DOID:10763 | hypertension | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:10591 | pre-eclampsia | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:6000 | congestive heart failure | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:0080326 | familial hypertrophic cardiomyopathy | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:0070242 | primary coenzyme Q10 deficiency 5 | HGNC:25302 | Homo sapiens (human) | 57017 | COQ9 |
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| DOID:0050730 | coenzyme Q10 deficiency disease | HGNC:25302 | Homo sapiens (human) | 57017 | COQ9 |
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| DOID:3204 | schwannomatosis | HGNC:20233 | Homo sapiens (human) | 51004 | COQ6 |
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| DOID:0070243 | primary coenzyme Q10 deficiency 6 | HGNC:20233 | Homo sapiens (human) | 51004 | COQ6 |
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| DOID:1184 | nephrotic syndrome | HGNC:20233 | Homo sapiens (human) | 51004 | COQ6 |
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| DOID:1184 | nephrotic syndrome | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:0050730 | coenzyme Q10 deficiency disease | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:0070238 | primary coenzyme Q10 deficiency 1 | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:10603 | glucose intolerance | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:4752 | multiple system atrophy | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:0111962 | combined immunodeficiency | HGNC:2236 | Homo sapiens (human) | 22820 | COPG1 |
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| DOID:2344 | polyclonal hypergammaglobulinemia | HGNC:2236 | Homo sapiens (human) | 22820 | COPG1 |
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| DOID:0070281 | primary autosomal recessive microcephaly 19 | HGNC:2232 | Homo sapiens (human) | 9276 | COPB2 |
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| DOID:10907 | microcephaly | HGNC:2232 | Homo sapiens (human) | 9276 | COPB2 |
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| DOID:0081242 | autoimmune interstitial lung, joint, and kidney disease | HGNC:2230 | Homo sapiens (human) | 1314 | COPA |
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| DOID:631 | fibromyalgia | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:9505 | cannabis abuse | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0050742 | nicotine dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:9976 | heroin dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:2560 | morphine dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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