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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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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:9273 | citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:0070341 | neonatal-onset type II citrullinemia | 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:4137 | common bile duct disease | 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:4137 | common bile duct disease | 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: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: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:12849 | autistic disorder | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:0050696 | fetal alcohol spectrum disorder | 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:0050773 | paraganglioma | HGNC:10981 | Homo sapiens (human) | 8402 | SLC25A11 |
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| DOID:0060475 | myoclonic-atonic epilepsy | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:0070450 | mitochondrial DNA depletion syndrome 19 | 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:0070329 | mitochondrial DNA depletion syndrome | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:10123 | pigmentation disease | HGNC:10978 | Homo sapiens (human) | 123041 | SLC24A4 |
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| DOID:0110063 | amelogenesis imperfecta hypomaturation type 2A5 | HGNC:10978 | Homo sapiens (human) | 123041 | SLC24A4 |
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| DOID:1826 | epilepsy | HGNC:10978 | Homo sapiens (human) | 123041 | SLC24A4 |
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| DOID:1826 | epilepsy | HGNC:10977 | Homo sapiens (human) | 57419 | SLC24A3 |
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| DOID:0110868 | congenital stationary night blindness 1D | HGNC:10975 | Homo sapiens (human) | 9187 | SLC24A1 |
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| DOID:6000 | congestive heart failure | HGNC:10969 | Homo sapiens (human) | 6584 | SLC22A5 |
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