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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:1852 | intrahepatic cholestasis | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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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:0050773 | paraganglioma | HGNC:10981 | Homo sapiens (human) | 8402 | SLC25A11 |
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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:3635 | congenital myasthenic syndrome | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:0050573 | 2-hydroxyglutaric aciduria | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:11198 | DiGeorge syndrome | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:0111619 | combined D-2- and L-2-hydroxyglutaric aciduria | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:700 | mitochondrial metabolism disease | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:3211 | lysosomal storage disease | HGNC:10933 | Homo sapiens (human) | 26503 | SLC17A5 |
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| DOID:3659 | sialuria | HGNC:10933 | Homo sapiens (human) | 26503 | SLC17A5 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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| DOID:224 | transient cerebral ischemia | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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| DOID:3911 | progeria | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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| DOID:9970 | obesity | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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