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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:0050793 | short QT syndrome | WB:WBGene00006830 | Caenorhabditis elegans | 175527 | unc-103 |
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| DOID:0110645 | long QT syndrome 2 | WB:WBGene00006830 | Caenorhabditis elegans | 175527 | unc-103 |
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| DOID:10273 | heart conduction disease | WB:WBGene00006830 | Caenorhabditis elegans | 175527 | unc-103 |
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| DOID:1826 | epilepsy | WB:WBGene00006830 | Caenorhabditis elegans | 175527 | unc-103 |
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| DOID:0050477 | Liddle syndrome | WB:WBGene00006832 | Caenorhabditis elegans | 174306 | unc-105 |
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| DOID:0080528 | bronchiectasis 3 | WB:WBGene00006832 | Caenorhabditis elegans | 174306 | unc-105 |
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| DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | WB:WBGene00006832 | Caenorhabditis elegans | 174306 | unc-105 |
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| DOID:4479 | pseudohypoaldosteronism | WB:WBGene00006832 | Caenorhabditis elegans | 174306 | unc-105 |
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| DOID:1184 | nephrotic syndrome | WB:WBGene00006832 | Caenorhabditis elegans | 174306 | unc-105 |
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| DOID:0080526 | bronchiectasis 1 | WB:WBGene00006832 | Caenorhabditis elegans | 174306 | unc-105 |
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| DOID:0110662 | congenital myasthenic syndrome 1B | WB:WBGene00006765 | Caenorhabditis elegans | 172703 | unc-29 |
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| DOID:0060682 | autosomal dominant nocturnal frontal lobe epilepsy 1 | WB:WBGene00006765 | Caenorhabditis elegans | 172703 | unc-29 |
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| DOID:809 | cocaine abuse | WB:WBGene00006765 | Caenorhabditis elegans | 172703 | unc-29 |
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| DOID:1574 | alcohol use disorder | WB:WBGene00006765 | Caenorhabditis elegans | 172703 | unc-29 |
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| DOID:0050742 | nicotine dependence | WB:WBGene00006765 | Caenorhabditis elegans | 172703 | unc-29 |
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| DOID:12217 | Lewy body dementia | WB:WBGene00006765 | Caenorhabditis elegans | 172703 | unc-29 |
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| DOID:10652 | Alzheimer's disease | WB:WBGene00006765 | Caenorhabditis elegans | 172703 | unc-29 |
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| DOID:0110663 | congenital myasthenic syndrome 1A | WB:WBGene00006765 | Caenorhabditis elegans | 172703 | unc-29 |
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| DOID:0070395 | developmental and epileptic encephalopathy 110 | WB:WBGene00006772 | Caenorhabditis elegans | 176155 | unc-36 |
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| DOID:10273 | heart conduction disease | WB:WBGene00006772 | Caenorhabditis elegans | 176155 | unc-36 |
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| DOID:3454 | brain infarction | WB:WBGene00006772 | Caenorhabditis elegans | 176155 | unc-36 |
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| DOID:1826 | epilepsy | WB:WBGene00006772 | Caenorhabditis elegans | 176155 | unc-36 |
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| DOID:0081023 | retinal cone dystrophy 4 | WB:WBGene00006772 | Caenorhabditis elegans | 176155 | unc-36 |
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| DOID:10534 | stomach cancer | WB:WBGene00006774 | Caenorhabditis elegans | 172105 | unc-38 |
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| DOID:3083 | chronic obstructive pulmonary disease | WB:WBGene00006774 | Caenorhabditis elegans | 172105 | unc-38 |
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