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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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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:10763 | hypertension | WB:WBGene00019127 | Caenorhabditis elegans | 174001 | cgt-3 |
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| DOID:0110669 | congenital myasthenic syndrome 14 | WB:WBGene00017282 | Caenorhabditis elegans | 173912 | algn-2 |
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| DOID:0080561 | congenital disorder of glycosylation Ii | WB:WBGene00017282 | Caenorhabditis elegans | 173912 | algn-2 |
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| DOID:9269 | maple syrup urine disease | HGNC:2898 | Homo sapiens (human) | 1738 | DLD |
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| DOID:0014667 | disease of metabolism | HGNC:2898 | Homo sapiens (human) | 1738 | DLD |
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| DOID:0060363 | glycerol kinase deficiency | WB:WBGene00020007 | Caenorhabditis elegans | 173747 | R11F4.1 |
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| DOID:13810 | familial hypercholesterolemia | WB:WBGene00020007 | Caenorhabditis elegans | 173747 | R11F4.1 |
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| DOID:3650 | lactic acidosis | HGNC:2896 | Homo sapiens (human) | 1737 | DLAT |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:2896 | Homo sapiens (human) | 1737 | DLAT |
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| DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | WB:WBGene00005020 | Caenorhabditis elegans | 173635 | sqv-2 |
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| DOID:0112198 | spondyloepimetaphyseal dysplasia with joint laxity type 1 | WB:WBGene00005020 | Caenorhabditis elegans | 173635 | sqv-2 |
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| DOID:13359 | Ehlers-Danlos syndrome | WB:WBGene00005020 | Caenorhabditis elegans | 173635 | sqv-2 |
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| DOID:12217 | Lewy body dementia | WB:WBGene00016335 | Caenorhabditis elegans | 173574 | gba-1 |
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| DOID:0110957 | Gaucher's disease type I | WB:WBGene00016335 | Caenorhabditis elegans | 173574 | gba-1 |
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| DOID:14330 | Parkinson's disease | WB:WBGene00016335 | Caenorhabditis elegans | 173574 | gba-1 |
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| DOID:1926 | Gaucher's disease | WB:WBGene00016335 | Caenorhabditis elegans | 173574 | gba-1 |
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| DOID:0110958 | Gaucher's disease type II | WB:WBGene00016335 | Caenorhabditis elegans | 173574 | gba-1 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0110443 | dilated cardiomyopathy 1B | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:9884 | muscular dystrophy | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0110444 | dilated cardiomyopathy 1X | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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