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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▲ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:3393 | coronary artery disease | WB:WBGene00020481 | Caenorhabditis elegans | 174116 | gldi-2 |
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| DOID:9452 | steatotic liver disease | WB:WBGene00020481 | Caenorhabditis elegans | 174116 | gldi-2 |
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| DOID:1168 | familial hyperlipidemia | WB:WBGene00020481 | Caenorhabditis elegans | 174116 | gldi-2 |
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| DOID:1312 | focal segmental glomerulosclerosis | WB:WBGene00020481 | Caenorhabditis elegans | 174116 | gldi-2 |
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| DOID:5419 | schizophrenia | WB:WBGene00020481 | Caenorhabditis elegans | 174116 | gldi-2 |
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| DOID:9074 | systemic lupus erythematosus | WB:WBGene00020481 | Caenorhabditis elegans | 174116 | gldi-2 |
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| DOID:10230 | aortic atherosclerosis | WB:WBGene00020481 | Caenorhabditis elegans | 174116 | gldi-2 |
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| DOID:5844 | myocardial infarction | WB:WBGene00020481 | Caenorhabditis elegans | 174116 | gldi-2 |
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| DOID:0110563 | autosomal dominant nonsyndromic deafness 36 | WB:WBGene00020490 | Caenorhabditis elegans | 188483 | tmc-1 |
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| DOID:10003 | sensorineural hearing loss | WB:WBGene00020490 | Caenorhabditis elegans | 188483 | tmc-1 |
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| DOID:0110520 | autosomal recessive nonsyndromic deafness 7 | WB:WBGene00020490 | Caenorhabditis elegans | 188483 | tmc-1 |
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| DOID:12556 | acute kidney tubular necrosis | WB:WBGene00020504 | Caenorhabditis elegans | 180929 | svh-2 |
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| DOID:10808 | gastric ulcer | WB:WBGene00020504 | Caenorhabditis elegans | 180929 | svh-2 |
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| DOID:12176 | goiter | WB:WBGene00020504 | Caenorhabditis elegans | 180929 | svh-2 |
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| DOID:5844 | myocardial infarction | WB:WBGene00020504 | Caenorhabditis elegans | 180929 | svh-2 |
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| DOID:2316 | brain ischemia | WB:WBGene00020504 | Caenorhabditis elegans | 180929 | svh-2 |
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| DOID:684 | hepatocellular carcinoma | WB:WBGene00020504 | Caenorhabditis elegans | 180929 | svh-2 |
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| DOID:12377 | spinal muscular atrophy | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:3323 | Sandhoff disease | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:3211 | lysosomal storage disease | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:3320 | Tay-Sachs disease | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:1919 | Lesch-Nyhan syndrome | WB:WBGene00020557 | Caenorhabditis elegans | 172232 | aprt-1 |
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| DOID:684 | hepatocellular carcinoma | WB:WBGene00020557 | Caenorhabditis elegans | 172232 | aprt-1 |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | WB:WBGene00020557 | Caenorhabditis elegans | 172232 | aprt-1 |
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| DOID:0050816 | urofacial syndrome | WB:WBGene00020649 | Caenorhabditis elegans | 176849 | sma-10 |
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