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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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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:13533 | osteopetrosis | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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| DOID:0110919 | hereditary spherocytosis type 4 | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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| DOID:589 | congenital hemolytic anemia | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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| DOID:2862 | glucosephosphate dehydrogenase deficiency | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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| DOID:0050793 | short QT syndrome | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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| DOID:11716 | prediabetes syndrome | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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| DOID:0050700 | cardiomyopathy | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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| DOID:12971 | hereditary spherocytosis | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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| DOID:11758 | iron deficiency anemia | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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| DOID:2373 | hereditary elliptocytosis | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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| DOID:0111153 | congenital mirror movement disorder | WB:WBGene00006746 | Caenorhabditis elegans | 180961 | unc-6 |
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| DOID:0060041 | autism spectrum disorder | WB:WBGene00016913 | Caenorhabditis elegans | 180980 | lam-2 |
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| DOID:5409 | lung small cell carcinoma | WB:WBGene00016913 | Caenorhabditis elegans | 180980 | lam-2 |
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| DOID:3907 | lung squamous cell carcinoma | WB:WBGene00016913 | Caenorhabditis elegans | 180980 | lam-2 |
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| DOID:3908 | lung non-small cell carcinoma | WB:WBGene00016913 | Caenorhabditis elegans | 180980 | lam-2 |
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| DOID:3209 | junctional epidermolysis bullosa | WB:WBGene00016913 | Caenorhabditis elegans | 180980 | lam-2 |
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| DOID:0060462 | Desbuquois dysplasia | WB:WBGene00017244 | Caenorhabditis elegans | 181019 | apy-1 |
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| DOID:0070302 | multiple epiphyseal dysplasia 7 | WB:WBGene00017244 | Caenorhabditis elegans | 181019 | apy-1 |
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| DOID:5844 | myocardial infarction | WB:WBGene00000083 | Caenorhabditis elegans | 181022 | adt-2 |
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| DOID:2316 | brain ischemia | WB:WBGene00000083 | Caenorhabditis elegans | 181022 | adt-2 |
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| DOID:11832 | visual epilepsy | WB:WBGene00000083 | Caenorhabditis elegans | 181022 | adt-2 |
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| DOID:5199 | ureteral obstruction | WB:WBGene00000083 | Caenorhabditis elegans | 181022 | adt-2 |
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| DOID:224 | transient cerebral ischemia | WB:WBGene00000083 | Caenorhabditis elegans | 181022 | adt-2 |
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| DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | WB:WBGene00000950 | Caenorhabditis elegans | 181035 | deg-1 |
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