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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: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: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:0050753 | cerebellar ataxia | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0110790 | hereditary spastic paraplegia 39 | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:1432 | blindness | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| 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:0050753 | cerebellar ataxia | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:1432 | blindness | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:1289 | neurodegenerative disease | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:0060256 | Dowling-Degos disease | HGNC:14988 | Homo sapiens (human) | 23509 | POFUT1 |
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