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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:299 | adenocarcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:1485 | cystic fibrosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0080855 | Parkinsonism | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:2384 | Wernicke encephalopathy | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:10763 | hypertension | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:14654 | prostatitis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:3770 | pulmonary fibrosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0060074 | ductal carcinoma in situ | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:3021 | acute kidney failure | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0060180 | colitis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:2316 | brain ischemia | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:3651 | pyruvate carboxylase deficiency disease | SGD:S000003030 | Saccharomyces cerevisiae S288C | 852818 | PYC1 |
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| DOID:3651 | pyruvate carboxylase deficiency disease | SGD:S000000422 | Saccharomyces cerevisiae S288C | 852519 | PYC2 |
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| DOID:3650 | lactic acidosis | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:2747 | glycogen storage disease | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:2754 | glycogen storage disease VI | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:2746 | glycogen storage disease V | HGNC:9726 | Homo sapiens (human) | 5837 | PYGM |
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| DOID:13580 | cholestasis | HGNC:9726 | Homo sapiens (human) | 5837 | PYGM |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | SGD:S000005874 | Saccharomyces cerevisiae S288C | 854529 | PYK2 |
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| DOID:9352 | type 2 diabetes mellitus | SGD:S000005874 | Saccharomyces cerevisiae S288C | 854529 | PYK2 |
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| DOID:0014667 | disease of metabolism | SGD:S000005874 | Saccharomyces cerevisiae S288C | 854529 | PYK2 |
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| DOID:0111077 | pyruvate kinase deficiency of red cells | SGD:S000005874 | Saccharomyces cerevisiae S288C | 854529 | PYK2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | SGD:S000005874 | Saccharomyces cerevisiae S288C | 854529 | PYK2 |
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| DOID:12365 | malaria | SGD:S000005874 | Saccharomyces cerevisiae S288C | 854529 | PYK2 |
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| DOID:1926 | Gaucher's disease | SGD:S000005874 | Saccharomyces cerevisiae S288C | 854529 | PYK2 |
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