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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0110676 | congenital myasthenic syndrome 13 | WB:WBGene00013362 | Caenorhabditis elegans | 190436 | algn-7 |
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| DOID:0080554 | congenital disorder of glycosylation Ib | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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| DOID:2978 | carbohydrate metabolic disorder | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | WB:WBGene00014098 | Caenorhabditis elegans | 179674 | ogdh-2 |
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| DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | WB:WBGene00014098 | Caenorhabditis elegans | 179674 | ogdh-2 |
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| DOID:0111459 | classic galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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| DOID:9870 | galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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| DOID:0080567 | congenital disorder of glycosylation Ip | WB:WBGene00015162 | Caenorhabditis elegans | 176032 | algn-11 |
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| DOID:0070311 | oligoasthenoteratozoospermia | WB:WBGene00015204 | Caenorhabditis elegans | 174243 | B0495.5 |
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| DOID:2747 | glycogen storage disease | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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| DOID:0111042 | glycogen storage disease IXa | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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| DOID:0050545 | visceral heterotaxy | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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| DOID:1459 | hypothyroidism | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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| DOID:0111040 | glycogen storage disease IXd | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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| DOID:0060256 | Dowling-Degos disease | WB:WBGene00015793 | Caenorhabditis elegans | 180607 | pfut-1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | WB:WBGene00015982 | Caenorhabditis elegans | 182795 | bgnt-1.4 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | WB:WBGene00015982 | Caenorhabditis elegans | 182795 | bgnt-1.4 |
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| DOID:14330 | Parkinson's disease | WB:WBGene00016204 | Caenorhabditis elegans | 183000 | gsto-1 |
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| DOID:10652 | Alzheimer's disease | WB:WBGene00016204 | Caenorhabditis elegans | 183000 | gsto-1 |
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| DOID:2841 | asthma | WB:WBGene00016204 | Caenorhabditis elegans | 183000 | gsto-1 |
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| DOID:13276 | Mycoplasma pneumoniae pneumonia | WB:WBGene00016207 | Caenorhabditis elegans | 183002 | C29E4.10 |
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| DOID:10587 | Krabbe disease | WB:WBGene00016207 | Caenorhabditis elegans | 183002 | C29E4.10 |
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| DOID:11949 | Creutzfeldt-Jakob disease | WB:WBGene00016207 | Caenorhabditis elegans | 183002 | C29E4.10 |
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| DOID:1909 | melanoma | WB:WBGene00016207 | Caenorhabditis elegans | 183002 | C29E4.10 |
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