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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: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:4795 | GM2 gangliosidosis, AB variant | MGI:95762 | Mus musculus (house mouse) | 14667 | Gm2a |
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| DOID:3321 | GM2 gangliosidosis | MGI:95762 | Mus musculus (house mouse) | 14667 | Gm2a |
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| DOID:2316 | brain ischemia | HGNC:2466 | Homo sapiens (human) | 1464 | CSPG4 |
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| DOID:2378 | relapsing-remitting multiple sclerosis | HGNC:2466 | Homo sapiens (human) | 1464 | CSPG4 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:2466 | Homo sapiens (human) | 1464 | CSPG4 |
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| DOID:83 | cataract | MGI:95730 | Mus musculus (house mouse) | 14635 | Galk1 |
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| DOID:14695 | galactokinase deficiency | MGI:95730 | Mus musculus (house mouse) | 14635 | Galk1 |
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| DOID:9675 | pulmonary emphysema | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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| DOID:5844 | myocardial infarction | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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| DOID:1485 | cystic fibrosis | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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| DOID:83 | cataract | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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| DOID:5082 | liver cirrhosis | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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| DOID:9256 | colorectal cancer | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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| DOID:583 | hemolytic anemia | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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| DOID:0111681 | glutamate-cysteine ligase deficiency | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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| DOID:0060363 | glycerol kinase deficiency | MGI:1329027 | Mus musculus (house mouse) | 14626 | Gk2 |
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| DOID:5844 | myocardial infarction | HGNC:2464 | Homo sapiens (human) | 1462 | VCAN |
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| DOID:10941 | intracranial aneurysm | HGNC:2464 | Homo sapiens (human) | 1462 | VCAN |
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| DOID:0110480 | autosomal recessive nonsyndromic deafness 22 | HGNC:16378 | Homo sapiens (human) | 146183 | OTOA |
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| DOID:0070256 | congenital disorder of glycosylation type IId | MGI:95705 | Mus musculus (house mouse) | 14595 | B4galt1 |
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| DOID:2986 | IgA glomerulonephritis | MGI:95705 | Mus musculus (house mouse) | 14595 | B4galt1 |
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