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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:3748 | esophagus squamous cell carcinoma | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:12894 | Sjogren's syndrome | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:10534 | stomach cancer | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:1380 | endometrial cancer | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:3069 | malignant astrocytoma | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:9743 | diabetic neuropathy | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:83 | cataract | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:783 | end stage renal disease | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:1184 | nephrotic syndrome | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:3393 | coronary artery disease | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:12140 | Chagas disease | HGNC:11177 | Homo sapiens (human) | 6646 | SOAT1 |
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| DOID:0070112 | Niemann-Pick disease type B | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:14504 | Niemann-Pick disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:0070111 | Niemann-Pick disease type A | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:893 | Wilson disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:9432 | renal glycosuria | HGNC:11037 | Homo sapiens (human) | 6524 | SLC5A2 |
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| DOID:10763 | hypertension | HGNC:11037 | Homo sapiens (human) | 6524 | SLC5A2 |
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| DOID:0080899 | lung pleomorphic carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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| DOID:2671 | transitional cell carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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| DOID:0050865 | tongue squamous cell carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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