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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:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:0070450 | mitochondrial DNA depletion syndrome 19 | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:0070329 | mitochondrial DNA depletion syndrome | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:0060536 | mitochondrial complex I deficiency | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:0060475 | myoclonic-atonic epilepsy | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:0050773 | paraganglioma | HGNC:10981 | Homo sapiens (human) | 8402 | SLC25A11 |
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| DOID:12849 | autistic disorder | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:4137 | common bile duct disease | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:0050432 | Asperger syndrome | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:0060041 | autism spectrum disorder | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:9273 | citrullinemia | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:1852 | intrahepatic cholestasis | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:0080349 | developmental and epileptic encephalopathy 39 | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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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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| DOID:1852 | intrahepatic cholestasis | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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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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