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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▲ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
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| DOID:0111974 | immunodeficiency 59 | WB:WBGene00020781 | Caenorhabditis elegans | 174033 | T24H7.2 |
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| DOID:5212 | congenital disorder of glycosylation | WB:WBGene00020820 | Caenorhabditis elegans | 175920 | algn-1 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | WB:WBGene00020820 | Caenorhabditis elegans | 175920 | algn-1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00020820 | Caenorhabditis elegans | 175920 | algn-1 |
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| DOID:3021 | acute kidney failure | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:2945 | severe acute respiratory syndrome | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:0111908 | thrombophilia due to thrombomodulin defect | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:0112313 | brain small vessel disease | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:10763 | hypertension | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:9074 | systemic lupus erythematosus | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:7147 | ankylosing spondylitis | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:3393 | coronary artery disease | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:10223 | dermatomyositis | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:10652 | Alzheimer's disease | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:1875 | impotence | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:2841 | asthma | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:9744 | type 1 diabetes mellitus | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:12132 | granulomatosis with polyangiitis | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:8577 | ulcerative colitis | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:326 | ischemia | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:11247 | disseminated intravascular coagulation | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:8778 | Crohn's disease | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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| DOID:783 | end stage renal disease | WB:WBGene00020921 | Caenorhabditis elegans | 180836 | W01C8.5 |
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