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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
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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▲ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0060639 | permanent neonatal diabetes mellitus | RGD:69247 | Rattus norvegicus (Norway rat) | 83535 | Kcnj11 |
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| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | RGD:69247 | Rattus norvegicus (Norway rat) | 83535 | Kcnj11 |
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| DOID:10763 | hypertension | RGD:69247 | Rattus norvegicus (Norway rat) | 83535 | Kcnj11 |
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| DOID:9352 | type 2 diabetes mellitus | RGD:69247 | Rattus norvegicus (Norway rat) | 83535 | Kcnj11 |
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| DOID:11832 | visual epilepsy | RGD:69247 | Rattus norvegicus (Norway rat) | 83535 | Kcnj11 |
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| DOID:0111110 | maturity-onset diabetes of the young type 13 | RGD:69247 | Rattus norvegicus (Norway rat) | 83535 | Kcnj11 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18619 | Homo sapiens (human) | 83548 | COG3 |
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| DOID:10763 | hypertension | RGD:621870 | Rattus norvegicus (Norway rat) | 83626 | Ugcg |
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| DOID:2978 | carbohydrate metabolic disorder | RGD:620674 | Rattus norvegicus (Norway rat) | 83688 | Taldo1 |
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| DOID:162 | cancer | HGNC:8994 | Homo sapiens (human) | 8394 | PIP5K1A |
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| DOID:162 | cancer | HGNC:8995 | Homo sapiens (human) | 8395 | PIP5K1B |
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| DOID:162 | cancer | HGNC:8998 | Homo sapiens (human) | 8396 | PIP4K2B |
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| DOID:0110736 | neurodegeneration with brain iron accumulation 2b | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:0060900 | Parkinson's disease 14 | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:0110735 | neurodegeneration with brain iron accumulation 2a | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:10247 | pleurisy | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:2367 | neuroaxonal dystrophy | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:0090056 | dystonia 12 | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:14330 | Parkinson's disease | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:1289 | neurodegenerative disease | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:0050773 | paraganglioma | HGNC:10981 | Homo sapiens (human) | 8402 | SLC25A11 |
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| DOID:2843 | long QT syndrome | RGD:621503 | Rattus norvegicus (Norway rat) | 84020 | Kcnq1 |
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| DOID:0050793 | short QT syndrome | RGD:621503 | Rattus norvegicus (Norway rat) | 84020 | Kcnq1 |
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| DOID:2842 | Jervell-Lange Nielsen syndrome | RGD:621503 | Rattus norvegicus (Norway rat) | 84020 | Kcnq1 |
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