DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
Source | Last Updated |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID ▲ | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0026918 | Mycobacterium Infections | FCN2 | 2220 | ficolin 2 | Q15485 |
C0017677 | Glossitis, Benign Migratory | FCN2 | 2220 | ficolin 2 | Q15485 |
C1704430 | Urinary Schistosomiasis | FCN2 | 2220 | ficolin 2 | Q15485 |
C0031099 | Periodontitis | FCN2 | 2220 | ficolin 2 | Q15485 |
C0398650 | Immune thrombocytopenic purpura | FCN2 | 2220 | ficolin 2 | Q15485 |
C0345967 | Malignant mesothelioma | FCN2 | 2220 | ficolin 2 | Q15485 |
C0027051 | Myocardial Infarction | FCN2 | 2220 | ficolin 2 | Q15485 |
C4721610 | Carcinoma, Ovarian Epithelial | FCN2 | 2220 | ficolin 2 | Q15485 |
C0279584 | Childhood B Acute Lymphoblastic Leukemia | FCN2 | 2220 | ficolin 2 | Q15485 |
C0040425 | Tonsillitis | FCN2 | 2220 | ficolin 2 | Q15485 |
C0033860 | Psoriasis | FCN2 | 2220 | ficolin 2 | Q15485 |
C0041234 | Chagas Disease | FCN2 | 2220 | ficolin 2 | Q15485 |
C0009447 | Common Variable Immunodeficiency | FCN2 | 2220 | ficolin 2 | Q15485 |
C0279593 | Adult B Acute Lymphoblastic Leukemia | FCN2 | 2220 | ficolin 2 | Q15485 |
C0021390 | Inflammatory Bowel Diseases | FCN2 | 2220 | ficolin 2 | Q15485 |
C0029463 | Osteosarcoma | FCN2 | 2220 | ficolin 2 | Q15485 |
C0036421 | Systemic Scleroderma | FCN2 | 2220 | ficolin 2 | Q15485 |
C0242379 | Malignant neoplasm of lung | FCN2 | 2220 | ficolin 2 | Q15485 |
C0206062 | Lung Diseases, Interstitial | FCN2 | 2220 | ficolin 2 | Q15485 |
C0035436 | Rheumatic Fever | FCN2 | 2220 | ficolin 2 | Q15485 |
C0027697 | Nephritis | FCN2 | 2220 | ficolin 2 | Q15485 |
C0004943 | Behcet Syndrome | FCN2 | 2220 | ficolin 2 | Q15485 |
C0409974 | Lupus Erythematosus | FCN2 | 2220 | ficolin 2 | Q15485 |
C0035204 | Respiration Disorders | FCN2 | 2220 | ficolin 2 | Q15485 |
C0276496 | Familial Alzheimer Disease (FAD) | FCN2 | 2220 | ficolin 2 | Q15485 |
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Last updated: August 19, 2024