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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:9252 | amino acid metabolic disorder | HGNC:10850 | Homo sapiens (human) | 6470 | SHMT1 |
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| DOID:0111818 | syndactyly type 4 | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:3328 | temporal lobe epilepsy | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:5844 | myocardial infarction | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:14679 | VACTERL association | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:0060071 | pre-malignant neoplasm | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:0060041 | autism spectrum disorder | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:2513 | basal cell carcinoma | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:10487 | Hirschsprung's disease | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:10534 | stomach cancer | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:3525 | middle cerebral artery infarction | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:784 | chronic kidney disease | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:0111380 | solitary median maxillary central incisor | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:0080171 | esophageal atresia/tracheoesophageal fistula | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:9256 | colorectal cancer | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:4621 | holoprosencephaly | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:2512 | nevoid basal cell carcinoma syndrome | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:10976 | membranous glomerulonephritis | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:0080855 | Parkinsonism | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:1148 | polydactyly | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:0050338 | primary bacterial infectious disease | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:2986 | IgA glomerulonephritis | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:1459 | hypothyroidism | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:0110875 | holoprosencephaly 3 | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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