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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:10763 | hypertension | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0090045 | childhood onset GLUT1 deficiency syndrome 2 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:2154 | nephroblastoma | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:10591 | pre-eclampsia | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:10487 | Hirschsprung's disease | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0111313 | idiopathic generalized epilepsy 12 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:1459 | hypothyroidism | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:1825 | childhood absence epilepsy | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:255 | hemangioma | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:10652 | Alzheimer's disease | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:9970 | obesity | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:14687 | diastrophic dysplasia | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:0070300 | multiple epiphyseal dysplasia 4 | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:0050648 | atelosteogenesis | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:2256 | osteochondrodysplasia | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:0050581 | brachydactyly | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:0080055 | achondrogenesis type IB | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:2300 | spondylolysis | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:0070341 | neonatal-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:9273 | citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:4137 | common bile duct disease | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:0070342 | adult-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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