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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: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: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: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: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: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: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:10763 | hypertension | WB:WBGene00019127 | Caenorhabditis elegans | 174001 | cgt-3 |
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| DOID:0070112 | Niemann-Pick disease type B | WB:WBGene00000211 | Caenorhabditis elegans | 174131 | asm-1 |
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| DOID:14504 | Niemann-Pick disease | WB:WBGene00000211 | Caenorhabditis elegans | 174131 | asm-1 |
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| DOID:893 | Wilson disease | WB:WBGene00000211 | Caenorhabditis elegans | 174131 | asm-1 |
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| DOID:0070111 | Niemann-Pick disease type A | WB:WBGene00000211 | Caenorhabditis elegans | 174131 | asm-1 |
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| DOID:0050775 | schneckenbecken dysplasia | WB:WBGene00005025 | Caenorhabditis elegans | 174145 | sqv-7 |
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| DOID:14227 | azoospermia | MGI:97040 | Mus musculus (house mouse) | 17423 | Ndst2 |
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| DOID:1059 | intellectual disability | MGI:97040 | Mus musculus (house mouse) | 17423 | Ndst2 |
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| DOID:0060041 | autism spectrum disorder | MGI:97040 | Mus musculus (house mouse) | 17423 | Ndst2 |
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| DOID:0070311 | oligoasthenoteratozoospermia | WB:WBGene00015204 | Caenorhabditis elegans | 174243 | B0495.5 |
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