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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:0080528 | bronchiectasis 3 | WB:WBGene00022815 | Caenorhabditis elegans | 191422 | asic-1 |
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| DOID:0050477 | Liddle syndrome | WB:WBGene00022815 | Caenorhabditis elegans | 191422 | asic-1 |
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| DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | WB:WBGene00022815 | Caenorhabditis elegans | 191422 | asic-1 |
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| DOID:1184 | nephrotic syndrome | WB:WBGene00022815 | Caenorhabditis elegans | 191422 | asic-1 |
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| DOID:4479 | pseudohypoaldosteronism | WB:WBGene00022815 | Caenorhabditis elegans | 191422 | asic-1 |
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| DOID:0080526 | bronchiectasis 1 | WB:WBGene00022815 | Caenorhabditis elegans | 191422 | asic-1 |
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| DOID:65 | connective tissue disease | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:4783 | mesangial proliferative glomerulonephritis | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:9352 | type 2 diabetes mellitus | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:3492 | mixed connective tissue disease | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:5082 | liver cirrhosis | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:0111561 | stiff skin syndrome | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:418 | systemic scleroderma | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:2921 | glomerulonephritis | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:0060218 | CREST syndrome | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:0060249 | scoliosis | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:988 | mitral valve prolapse | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:114 | heart disease | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:0050475 | Weill-Marchesani syndrome | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:0111150 | autosomal dominant isolated ectopia lentis 1 | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:10763 | hypertension | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:0111726 | geleophysic dysplasia 2 | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:3627 | aortic aneurysm | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:0050646 | distal arthrogryposis | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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| DOID:0111595 | congenital contractural arachnodactyly | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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