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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:2749 | glycogen storage disease Ia | HGNC:4056 | Homo sapiens (human) | 2538 | G6PC1 |
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| DOID:0060849 | osteoporosis-pseudoglioma syndrome | MGI:1278315 | Mus musculus (house mouse) | 16973 | Lrp5 |
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| DOID:784 | chronic kidney disease | RGD:620396 | Rattus norvegicus (Norway rat) | 83504 | Kl |
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| DOID:1926 | Gaucher's disease | MGI:95665 | Mus musculus (house mouse) | 14466 | Gba1 |
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| DOID:6432 | pulmonary hypertension | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:2842 | Jervell-Lange Nielsen syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:10763 | hypertension | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:0080119 | mitochondrial DNA depletion syndrome 1 | MGI:1920212 | Mus musculus (house mouse) | 72962 | Tymp |
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| DOID:12918 | thromboangiitis obliterans | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:9206 | Barrett's esophagus | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:5844 | myocardial infarction | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:9655 | oral mucosa leukoplakia | RGD:3889 | Rattus norvegicus (Norway rat) | 24842 | Tp53 |
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| DOID:5844 | myocardial infarction | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:5844 | myocardial infarction | HGNC:9053 | Homo sapiens (human) | 5329 | PLAUR |
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| DOID:0060001 | withdrawal disorder | RGD:61800 | Rattus norvegicus (Norway rat) | 29595 | Htr2a |
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| DOID:10652 | Alzheimer's disease | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:13359 | Ehlers-Danlos syndrome | WB:WBGene00005021 | Caenorhabditis elegans | 176382 | sqv-3 |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0060062 | familial juvenile hyperuricemic nephropathy | HGNC:12559 | Homo sapiens (human) | 7369 | UMOD |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:9970 | obesity | RGD:2796 | Rattus norvegicus (Norway rat) | 25058 | Hk1 |
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