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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:0110861 | autosomal recessive polycystic kidney disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3587 | pancreatic ductal carcinoma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:8432 | polycythemia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:418 | systemic scleroderma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3770 | pulmonary fibrosis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:12236 | primary biliary cholangitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3905 | lung carcinoma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0060071 | pre-malignant neoplasm | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0080572 | congenital disorder of glycosylation Iw | MGI:105124 | Mus musculus (house mouse) | 16430 | Stt3a |
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| DOID:9970 | obesity | HGNC:384 | Homo sapiens (human) | 1645 | AKR1C1 |
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| DOID:0111773 | 46,XY sex reversal 8 | HGNC:385 | Homo sapiens (human) | 1646 | AKR1C2 |
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| DOID:9970 | obesity | HGNC:385 | Homo sapiens (human) | 1646 | AKR1C2 |
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| DOID:0080569 | congenital disorder of glycosylation Ir | HGNC:2728 | Homo sapiens (human) | 1650 | DDOST |
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| DOID:0111110 | maturity-onset diabetes of the young type 13 | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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| DOID:9351 | diabetes mellitus | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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| DOID:0080855 | Parkinsonism | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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| DOID:11446 | sciatic neuropathy | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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| DOID:0060639 | permanent neonatal diabetes mellitus | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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| DOID:2018 | hyperinsulinism | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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| DOID:11832 | visual epilepsy | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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| DOID:10763 | hypertension | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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| DOID:11716 | prediabetes syndrome | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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