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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
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:8947 | diabetic retinopathy | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:5844 | myocardial infarction | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:10763 | hypertension | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:418 | systemic scleroderma | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:2224 | essential thrombocythemia | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:9970 | obesity | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:12531 | von Willebrand's disease | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:13241 | Behcet's disease | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:13809 | familial combined hyperlipidemia | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:4783 | mesangial proliferative glomerulonephritis | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:10941 | intracranial aneurysm | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:0111054 | von Willebrand's disease 3 | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:3312 | bipolar disorder | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:3770 | pulmonary fibrosis | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:576 | proteinuria | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:12132 | granulomatosis with polyangiitis | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:8947 | diabetic retinopathy | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:3049 | Churg-Strauss syndrome | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:0060903 | thrombosis | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:3393 | coronary artery disease | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:11832 | visual epilepsy | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:5844 | myocardial infarction | HGNC:12716 | Homo sapiens (human) | 7442 | TRPV1 |
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| DOID:6364 | migraine | HGNC:12716 | Homo sapiens (human) | 7442 | TRPV1 |
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| DOID:2548 | reflex epilepsy | HGNC:12716 | Homo sapiens (human) | 7442 | TRPV1 |
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