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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:809 | cocaine abuse | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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| DOID:14330 | Parkinson's disease | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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| DOID:1596 | depressive disorder | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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| DOID:0110681 | congenital myasthenic syndrome 2A | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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| DOID:0110678 | congenital myasthenic syndrome 4A | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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| DOID:3905 | lung carcinoma | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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| DOID:5409 | lung small cell carcinoma | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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| DOID:1094 | attention deficit hyperactivity disorder | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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| DOID:0060684 | autosomal dominant nocturnal frontal lobe epilepsy 3 | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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| DOID:0080434 | developmental and epileptic encephalopathy 61 | WB:WBGene00006804 | Caenorhabditis elegans | 176706 | unc-71 |
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| DOID:4194 | glucose metabolism disease | WB:WBGene00006830 | Caenorhabditis elegans | 175527 | unc-103 |
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| DOID:2843 | long QT syndrome | WB:WBGene00006830 | Caenorhabditis elegans | 175527 | unc-103 |
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| 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:0050579 | glycogen storage disease XV | WB:WBGene00006863 | Caenorhabditis elegans | 180644 | gyg-1 |
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| DOID:3748 | esophagus squamous cell carcinoma | WB:WBGene00006868 | Caenorhabditis elegans | 173794 | vab-1 |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | WB:WBGene00006868 | Caenorhabditis elegans | 173794 | vab-1 |
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