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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:12930 | dilated cardiomyopathy | WB:WBGene00000833 | Caenorhabditis elegans | 176437 | cts-1 |
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| DOID:0050852 | limb ischemia | WB:WBGene00000833 | Caenorhabditis elegans | 176437 | cts-1 |
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| DOID:3312 | bipolar disorder | WB:WBGene00000833 | Caenorhabditis elegans | 176437 | cts-1 |
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| DOID:1459 | hypothyroidism | WB:WBGene00000833 | Caenorhabditis elegans | 176437 | cts-1 |
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| DOID:5844 | myocardial infarction | WB:WBGene00000833 | Caenorhabditis elegans | 176437 | cts-1 |
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| DOID:6000 | congestive heart failure | WB:WBGene00000833 | Caenorhabditis elegans | 176437 | cts-1 |
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| DOID:11984 | hypertrophic cardiomyopathy | WB:WBGene00000833 | Caenorhabditis elegans | 176437 | cts-1 |
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| DOID:8466 | retinal degeneration | WB:WBGene00000833 | Caenorhabditis elegans | 176437 | cts-1 |
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| DOID:7998 | hyperthyroidism | WB:WBGene00000833 | Caenorhabditis elegans | 176437 | cts-1 |
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| DOID:653 | purine-pyrimidine metabolic disorder | WB:WBGene00011559 | Caenorhabditis elegans | 176453 | umps-1 |
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| DOID:0050833 | orotic aciduria | WB:WBGene00011559 | Caenorhabditis elegans | 176453 | umps-1 |
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| DOID:0060050 | autoimmune disease of blood | WB:WBGene00008019 | Caenorhabditis elegans | 176455 | C38H2.2 |
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| DOID:206 | hereditary multiple exostoses | WB:WBGene00004361 | Caenorhabditis elegans | 176502 | rib-2 |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | WB:WBGene00013241 | Caenorhabditis elegans | 176633 | ung-1 |
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| DOID:11702 | dysgammaglobulinemia | WB:WBGene00013241 | Caenorhabditis elegans | 176633 | ung-1 |
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| DOID:9256 | colorectal cancer | WB:WBGene00001630 | Caenorhabditis elegans | 176736 | gly-5 |
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| DOID:9869 | hereditary fructose intolerance syndrome | WB:WBGene00011474 | Caenorhabditis elegans | 176788 | aldo-1 |
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| DOID:438 | autoimmune disease of the nervous system | WB:WBGene00011474 | Caenorhabditis elegans | 176788 | aldo-1 |
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| DOID:8283 | peritonitis | WB:WBGene00011474 | Caenorhabditis elegans | 176788 | aldo-1 |
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| DOID:684 | hepatocellular carcinoma | WB:WBGene00011474 | Caenorhabditis elegans | 176788 | aldo-1 |
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| DOID:916 | liver benign neoplasm | WB:WBGene00011474 | Caenorhabditis elegans | 176788 | aldo-1 |
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| DOID:5154 | borna disease | WB:WBGene00011474 | Caenorhabditis elegans | 176788 | aldo-1 |
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| DOID:9352 | type 2 diabetes mellitus | WB:WBGene00011474 | Caenorhabditis elegans | 176788 | aldo-1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00022044 | Caenorhabditis elegans | 176874 | dpm-1 |
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| DOID:0080557 | congenital disorder of glycosylation Ie | WB:WBGene00022044 | Caenorhabditis elegans | 176874 | dpm-1 |
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