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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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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:9352 | type 2 diabetes mellitus | HGNC:224 | Homo sapiens (human) | 11095 | ADAMTS8 |
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| DOID:9970 | obesity | HGNC:224 | Homo sapiens (human) | 11095 | ADAMTS8 |
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| DOID:10772 | thrombotic thrombocytopenic purpura | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:0080177 | hepatic veno-occlusive disease | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:13133 | HELLP syndrome | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:11247 | disseminated intravascular coagulation | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:5082 | liver cirrhosis | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:418 | systemic scleroderma | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:13580 | cholestasis | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:14067 | Plasmodium falciparum malaria | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:162 | cancer | MGI:1332236 | Mus musculus (house mouse) | 110911 | Cds2 |
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| DOID:1682 | congenital heart disease | HGNC:12757 | Homo sapiens (human) | 11091 | WDR5 |
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| DOID:3635 | congenital myasthenic syndrome | MGI:87886 | Mus musculus (house mouse) | 110902 | Chrna2 |
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| DOID:0060685 | autosomal dominant nocturnal frontal lobe epilepsy 4 | MGI:87886 | Mus musculus (house mouse) | 110902 | Chrna2 |
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| DOID:1574 | alcohol use disorder | MGI:87886 | Mus musculus (house mouse) | 110902 | Chrna2 |
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| DOID:0081119 | benign familial infantile seizures 6 | MGI:87886 | Mus musculus (house mouse) | 110902 | Chrna2 |
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| DOID:0111773 | 46,XY sex reversal 8 | HGNC:387 | Homo sapiens (human) | 1109 | AKR1C4 |
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| DOID:585 | nephrolithiasis | MGI:105074 | Mus musculus (house mouse) | 110895 | Slc9a4 |
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| DOID:10652 | Alzheimer's disease | MGI:107976 | Mus musculus (house mouse) | 110893 | Slc8a3 |
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| DOID:2316 | brain ischemia | MGI:107976 | Mus musculus (house mouse) | 110893 | Slc8a3 |
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| DOID:1824 | status epilepticus | MGI:107976 | Mus musculus (house mouse) | 110893 | Slc8a3 |
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| DOID:2316 | brain ischemia | MGI:107996 | Mus musculus (house mouse) | 110891 | Slc8a2 |
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