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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:8534 | gastroesophageal reflux disease | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:9256 | colorectal cancer | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:11151 | cholecystolithiasis | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:0014667 | disease of metabolism | HGNC:9021 | Homo sapiens (human) | 5315 | PKM |
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| DOID:10763 | hypertension | HGNC:9021 | Homo sapiens (human) | 5315 | PKM |
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| DOID:1926 | Gaucher's disease | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:12365 | malaria | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0014667 | disease of metabolism | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:4195 | hyperglycemia | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0111077 | pyruvate kinase deficiency of red cells | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0060340 | ciliopathy | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:3021 | acute kidney failure | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:8466 | retinal degeneration | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:0110859 | polycystic kidney disease 2 | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:10941 | intracranial aneurysm | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:0080322 | polycystic kidney disease | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:10941 | intracranial aneurysm | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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