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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:1574 | alcohol use disorder | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:0050742 | nicotine dependence | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:5844 | myocardial infarction | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:1793 | pancreatic cancer | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:0050933 | ovarian serous carcinoma | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:10652 | Alzheimer's disease | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:10754 | otitis media | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
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| DOID:0110178 | Charcot-Marie-Tooth disease axonal type 2V | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
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| DOID:0111394 | mucopolysaccharidosis type IIIB | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
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| DOID:479 | angiokeratoma | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:0112318 | Schindler disease type 1 | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:0112319 | Kanzaki disease | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:2367 | neuroaxonal dystrophy | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:14499 | Fabry disease | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:5517 | stomach carcinoma | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:0080410 | familial adenomatous polyposis 2 | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:0050424 | familial adenomatous polyposis | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:10534 | stomach cancer | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:0060740 | methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency | HGNC:7526 | Homo sapiens (human) | 4594 | MMUT |
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| DOID:14749 | methylmalonic acidemia | HGNC:7526 | Homo sapiens (human) | 4594 | MMUT |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
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| DOID:14717 | centronuclear myopathy | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7453 | Homo sapiens (human) | 9107 | MTMR6 |
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