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 |
---|---|
DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▼ |
---|---|---|---|---|---|
C0011991 | Diarrhea | RGN | 9104 | regucalcin | Q15493 |
C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | RGN | 9104 | regucalcin | Q15493 |
C0023895 | Liver diseases | RGN | 9104 | regucalcin | Q15493 |
C0020476 | Hyperlipoproteinemias | RGN | 9104 | regucalcin | Q15493 |
C0023890 | Liver Cirrhosis | RGN | 9104 | regucalcin | Q15493 |
C0029442 | Osteomalacia | RGN | 9104 | regucalcin | Q15493 |
C0162557 | Liver Failure, Acute | RGN | 9104 | regucalcin | Q15493 |
C0007131 | Non-Small Cell Lung Carcinoma | RGN | 9104 | regucalcin | Q15493 |
C0684249 | Carcinoma of lung | RGN | 9104 | regucalcin | Q15493 |
C0020538 | Hypertensive disease | RGN | 9104 | regucalcin | Q15493 |
C0346647 | Malignant neoplasm of pancreas | RGN | 9104 | regucalcin | Q15493 |
C2676033 | Hepatoblastoma Caused By Somatic Mutation | RGN | 9104 | regucalcin | Q15493 |
C0001418 | Adenocarcinoma | RGN | 9104 | regucalcin | Q15493 |
C0011581 | Depressive disorder | RGN | 9104 | regucalcin | Q15493 |
C0035078 | Kidney Failure | RGN | 9104 | regucalcin | Q15493 |
C0034067 | Pulmonary Emphysema | RGN | 9104 | regucalcin | Q15493 |
C1378703 | Renal carcinoma | RGN | 9104 | regucalcin | Q15493 |
C0268547 | Argininosuccinic Aciduria | RGN | 9104 | regucalcin | Q15493 |
C0022658 | Kidney Diseases | RGN | 9104 | regucalcin | Q15493 |
C0699790 | Colon Carcinoma | RGN | 9104 | regucalcin | Q15493 |
C0917713 | Becker Muscular Dystrophy | RGN | 9104 | regucalcin | Q15493 |
C0011570 | Mental Depression | RGN | 9104 | regucalcin | Q15493 |
C0339510 | Vitelliform Macular Dystrophy | RGN | 9104 | regucalcin | Q15493 |
C0009402 | Colorectal Carcinoma | RGN | 9104 | regucalcin | Q15493 |
C0750901 | Alzheimer Disease, Early Onset | FCN2 | 2220 | ficolin 2 | Q15485 |
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Last updated: August 19, 2024