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GlyTouCan
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:2394 | ovarian cancer | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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| DOID:3459 | breast carcinoma | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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| DOID:0110210 | Charcot-Marie-Tooth disease X-linked recessive 5 | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0111260 | phosphoribosylpyrophosphate synthetase superactivity | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0111739 | X-linked deafness 1 | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0050647 | Arts syndrome | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:13189 | gout | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0090103 | Huntington's disease-like 1 | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:5434 | scrapie | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:4249 | Gerstmann-Straussler-Scheinker syndrome | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0050433 | fatal familial insomnia | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:4195 | hyperglycemia | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:11949 | Creutzfeldt-Jakob disease | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:648 | kuru | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:409 | liver disease | HGNC:9411 | Homo sapiens (human) | 5589 | PRKCSH |
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| DOID:0050770 | polycystic liver disease | HGNC:9411 | Homo sapiens (human) | 5589 | PRKCSH |
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| DOID:1289 | neurodegenerative disease | HGNC:9387 | Homo sapiens (human) | 53632 | PRKAG3 |
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| DOID:0090101 | lethal congenital glycogen storage disease of heart | HGNC:9387 | Homo sapiens (human) | 53632 | PRKAG3 |
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| DOID:384 | Wolff-Parkinson-White syndrome | HGNC:9387 | Homo sapiens (human) | 53632 | PRKAG3 |
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| DOID:384 | Wolff-Parkinson-White syndrome | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:2747 | glycogen storage disease | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:0110312 | hypertrophic cardiomyopathy 6 | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:0090101 | lethal congenital glycogen storage disease of heart | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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