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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▼ |
|---|---|---|---|---|---|---|---|---|
| DOID:350 | mastocytosis | MGI:96677 | Mus musculus (house mouse) | 16590 | Kit |
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| DOID:0080855 | Parkinsonism | RGD:2677 | Rattus norvegicus (Norway rat) | 25453 | Gdnf |
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| DOID:9970 | obesity | HGNC:6526 | Homo sapiens (human) | 3934 | LCN2 |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:6342 | Homo sapiens (human) | 3815 | KIT |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:784 | chronic kidney disease | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:784 | chronic kidney disease | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:2750 | glycogen storage disease IV | MGI:1921435 | Mus musculus (house mouse) | 74185 | Gbe1 |
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| DOID:14756 | vascular type Ehlers-Danlos syndrome | MGI:88453 | Mus musculus (house mouse) | 12825 | Col3a1 |
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| DOID:0050741 | alcohol dependence | HGNC:281 | Homo sapiens (human) | 150 | ADRA2A |
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| DOID:856 | biotinidase deficiency | MGI:1347001 | Mus musculus (house mouse) | 26363 | Btd |
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| DOID:5844 | myocardial infarction | RGD:2411 | Rattus norvegicus (Norway rat) | 25419 | Crp |
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| DOID:10763 | hypertension | RGD:2070 | Rattus norvegicus (Norway rat) | 24180 | Agtr1a |
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| DOID:0060773 | cleft lip-palate-ectodermal dysplasia syndrome | MGI:1926483 | Mus musculus (house mouse) | 58235 | Nectin1 |
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| DOID:5419 | schizophrenia | HGNC:6381 | Homo sapiens (human) | 8564 | KMO |
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| DOID:0060700 | familial hypocalciuric hypercalcemia 1 | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:9970 | obesity | RGD:2857 | Rattus norvegicus (Norway rat) | 25464 | Icam1 |
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| DOID:12217 | Lewy body dementia | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:3635 | congenital myasthenic syndrome | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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| DOID:6364 | migraine | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:14791 | Leber congenital amaurosis | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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| DOID:2841 | asthma | RGD:2857 | Rattus norvegicus (Norway rat) | 25464 | Icam1 |
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| DOID:5844 | myocardial infarction | RGD:620597 | Rattus norvegicus (Norway rat) | 50692 | Plaur |
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| DOID:2377 | multiple sclerosis | HGNC:9360 | Homo sapiens (human) | 5551 | PRF1 |
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