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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:0111271 | Oliver-McFarlane syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0111265 | Boucher-Neuhauser syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:1289 | neurodegenerative disease | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:1930 | Laurence-Moon syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:1459 | hypothyroidism | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:3393 | coronary artery disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:9970 | obesity | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0050729 | Chanarin-Dorfman syndrome | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0060158 | acquired metabolic disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:5082 | liver cirrhosis | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:9452 | steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:9970 | obesity | HGNC:30802 | Homo sapiens (human) | 57104 | PNPLA2 |
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| DOID:0050729 | Chanarin-Dorfman syndrome | HGNC:30802 | Homo sapiens (human) | 57104 | PNPLA2 |
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| DOID:0060158 | acquired metabolic disease | HGNC:30802 | Homo sapiens (human) | 57104 | PNPLA2 |
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| DOID:5813 | purine nucleoside phosphorylase deficiency | SGD:S000004199 | Saccharomyces cerevisiae S288C | 850906 | PNP1 |
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| DOID:653 | purine-pyrimidine metabolic disorder | SGD:S000004199 | Saccharomyces cerevisiae S288C | 850906 | PNP1 |
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| DOID:653 | purine-pyrimidine metabolic disorder | HGNC:7892 | Homo sapiens (human) | 4860 | PNP |
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| DOID:5813 | purine nucleoside phosphorylase deficiency | HGNC:7892 | Homo sapiens (human) | 4860 | PNP |
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| DOID:10283 | prostate cancer | HGNC:9156 | Homo sapiens (human) | 5407 | PNLIPRP1 |
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| DOID:9970 | obesity | HGNC:9155 | Homo sapiens (human) | 5406 | PNLIP |
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| DOID:9884 | muscular dystrophy | SGD:S000003431 | Saccharomyces cerevisiae S288C | 853113 | PMT6 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | SGD:S000003431 | Saccharomyces cerevisiae S288C | 853113 | PMT6 |
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