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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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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:3748 | esophagus squamous cell carcinoma | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:1793 | pancreatic cancer | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:0080199 | colorectal carcinoma | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:11054 | urinary bladder cancer | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:219 | colon cancer | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:2394 | ovarian cancer | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:3458 | breast adenocarcinoma | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:10283 | prostate cancer | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:5683 | hereditary breast ovarian cancer syndrome | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:2256 | osteochondrodysplasia | 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:0070300 | multiple epiphyseal dysplasia 4 | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:14687 | diastrophic dysplasia | 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:0050648 | atelosteogenesis | 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:0050581 | brachydactyly | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:0080652 | calcium oxalate nephrolithiasis | HGNC:10993 | Homo sapiens (human) | 10861 | SLC26A1 |
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| DOID:1826 | epilepsy | HGNC:10992 | Homo sapiens (human) | 293 | SLC25A6 |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:10992 | Homo sapiens (human) | 293 | SLC25A6 |
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| DOID:700 | mitochondrial metabolism disease | HGNC:10992 | Homo sapiens (human) | 293 | SLC25A6 |
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| DOID:0080335 | mitochondrial DNA depletion syndrome 12b | HGNC:10992 | Homo sapiens (human) | 293 | SLC25A6 |
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| DOID:0111517 | autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 | HGNC:10992 | Homo sapiens (human) | 293 | SLC25A6 |
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| DOID:12361 | Graves' disease | HGNC:10986 | Homo sapiens (human) | 8034 | SLC25A16 |
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