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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:10941 | intracranial aneurysm | HGNC:2464 | Homo sapiens (human) | 1462 | VCAN |
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| DOID:3498 | pancreatic ductal adenocarcinoma | HGNC:12705 | Homo sapiens (human) | 8876 | VNN1 |
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| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:9884 | muscular dystrophy | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0110444 | dilated cardiomyopathy 1X | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0050560 | Walker-Warburg syndrome | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0110443 | dilated cardiomyopathy 1B | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:14500 | fucosidosis | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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| DOID:9352 | type 2 diabetes mellitus | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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| DOID:9744 | type 1 diabetes mellitus | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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| DOID:8947 | diabetic retinopathy | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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| DOID:9351 | diabetes mellitus | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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| DOID:0080569 | congenital disorder of glycosylation Ir | SGD:S000000728 | Saccharomyces cerevisiae S288C | 856716 | WBP1 |
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| DOID:1682 | congenital heart disease | HGNC:12757 | Homo sapiens (human) | 11091 | WDR5 |
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| DOID:9970 | obesity | HGNC:29175 | Homo sapiens (human) | 23038 | WDTC1 |
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| DOID:0060041 | autism spectrum disorder | MGI:1096875 | Mus musculus (house mouse) | 72145 | Wdfy3 |
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| DOID:2935 | Chediak-Higashi syndrome | MGI:1096875 | Mus musculus (house mouse) | 72145 | Wdfy3 |
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| DOID:0070295 | primary autosomal dominant microcephaly 18 | MGI:1096875 | Mus musculus (house mouse) | 72145 | Wdfy3 |
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| DOID:1682 | congenital heart disease | MGI:2155884 | Mus musculus (house mouse) | 140858 | Wdr5 |
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| DOID:1682 | congenital heart disease | RGD:1305159 | Rattus norvegicus (Norway rat) | 362093 | Wdr5 |
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| DOID:9970 | obesity | MGI:2685541 | Mus musculus (house mouse) | 230796 | Wdtc1 |
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