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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:11984 | hypertrophic cardiomyopathy | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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| DOID:9256 | colorectal cancer | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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| DOID:0112002 | immunodeficiency 47 | WB:WBGene00021952 | Caenorhabditis elegans | 177103 | vha-19 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00022044 | Caenorhabditis elegans | 176874 | dpm-1 |
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| DOID:0080557 | congenital disorder of glycosylation Ie | WB:WBGene00022044 | Caenorhabditis elegans | 176874 | dpm-1 |
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| DOID:5419 | schizophrenia | WB:WBGene00022076 | Caenorhabditis elegans | 3565775 | daao-1 |
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| DOID:11446 | sciatic neuropathy | WB:WBGene00022154 | Caenorhabditis elegans | 190602 | drag-1 |
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| DOID:3525 | middle cerebral artery infarction | WB:WBGene00022154 | Caenorhabditis elegans | 190602 | drag-1 |
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| DOID:3328 | temporal lobe epilepsy | WB:WBGene00022154 | Caenorhabditis elegans | 190602 | drag-1 |
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| DOID:2352 | hemochromatosis | WB:WBGene00022154 | Caenorhabditis elegans | 190602 | drag-1 |
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| DOID:2377 | multiple sclerosis | WB:WBGene00022154 | Caenorhabditis elegans | 190602 | drag-1 |
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| DOID:0111027 | hemochromatosis type 2A | WB:WBGene00022154 | Caenorhabditis elegans | 190602 | drag-1 |
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| DOID:0014667 | disease of metabolism | WB:WBGene00022199 | Caenorhabditis elegans | 180583 | pfk-1.1 |
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| DOID:11721 | glycogen storage disease VII | WB:WBGene00022199 | Caenorhabditis elegans | 180583 | pfk-1.1 |
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| DOID:2747 | glycogen storage disease | WB:WBGene00022199 | Caenorhabditis elegans | 180583 | pfk-1.1 |
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| DOID:0080201 | Peters plus syndrome | WB:WBGene00022576 | Caenorhabditis elegans | 178968 | ZC250.2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00022629 | Caenorhabditis elegans | 179185 | algn-12 |
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| DOID:0080559 | congenital disorder of glycosylation Ig | WB:WBGene00022629 | Caenorhabditis elegans | 179185 | algn-12 |
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| DOID:14497 | Wolman disease | WB:WBGene00022642 | Caenorhabditis elegans | 178563 | lipl-5 |
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| DOID:0080217 | lysosomal acid lipase deficiency | WB:WBGene00022642 | Caenorhabditis elegans | 178563 | lipl-5 |
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| DOID:14502 | cholesterol ester storage disease | WB:WBGene00022642 | Caenorhabditis elegans | 178563 | lipl-5 |
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| DOID:0060717 | autosomal recessive congenital ichthyosis 8 | WB:WBGene00022642 | Caenorhabditis elegans | 178563 | lipl-5 |
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| DOID:1574 | alcohol use disorder | WB:WBGene00022675 | Caenorhabditis elegans | 191240 | gbb-2 |
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| DOID:0080291 | developmental and epileptic encephalopathy 59 | WB:WBGene00022675 | Caenorhabditis elegans | 191240 | gbb-2 |
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| DOID:0050742 | nicotine dependence | WB:WBGene00022675 | Caenorhabditis elegans | 191240 | gbb-2 |
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