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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
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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:1123 | spondyloarthropathy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080600 | COVID-19 | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
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| DOID:10762 | portal hypertension | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3492 | mixed connective tissue disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
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| DOID:12662 | paracoccidioidomycosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080162 | lupus nephritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:841 | extrinsic allergic alveolitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:9452 | steatotic liver disease | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:9970 | obesity | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:906 | peroxisomal disease | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:0070516 | Mitchell syndrome | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:219 | colon cancer | HGNC:11906 | Homo sapiens (human) | 8794 | TNFRSF10C |
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| DOID:8398 | osteoarthritis | HGNC:11906 | Homo sapiens (human) | 8794 | TNFRSF10C |
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| DOID:0080202 | adenoid cystic carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3347 | osteosarcoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:12361 | Graves' disease | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3070 | high grade glioma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3068 | glioblastoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3744 | cervical squamous cell carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3702 | cervical adenocarcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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