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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0070218 | familial hyperinsulinemic hypoglycemia 2 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:10763 | hypertension | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:11716 | prediabetes syndrome | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:11446 | sciatic neuropathy | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:11832 | visual epilepsy | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:2018 | hyperinsulinism | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:1824 | status epilepticus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0080855 | Parkinsonism | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0111110 | maturity-onset diabetes of the young type 13 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0060224 | atrial fibrillation | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:2842 | Jervell-Lange Nielsen syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:2843 | long QT syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:0050793 | short QT syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:0050650 | familial atrial fibrillation | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:4440 | seminoma | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:10763 | hypertension | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:0110644 | long QT syndrome 1 | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:0050873 | follicular lymphoma | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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| DOID:0080250 | erythrokeratodermia variabilis et progressiva 4 | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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| DOID:409 | liver disease | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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| DOID:1588 | thrombocytopenia | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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| DOID:0111680 | essential fructosuria | HGNC:6315 | Homo sapiens (human) | 3795 | KHK |
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