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 |
---|---|---|---|---|---|
C0162429 | Malnutrition | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0947622 | Cholecystolithiasis | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0023903 | Liver neoplasms | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0008312 | Primary biliary cirrhosis | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0023895 | Liver diseases | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0020538 | Hypertensive disease | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0042870 | Vitamin D Deficiency | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0007222 | Cardiovascular Diseases | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0020473 | Hyperlipidemia | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0028754 | Obesity | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0020445 | Hypercholesterolemia, Familial | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0020550 | Hyperthyroidism | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0011847 | Diabetes | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0019187 | Hepatitis, Alcoholic | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0206624 | Hepatoblastoma | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0235782 | Gallbladder Carcinoma | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0011854 | Diabetes Mellitus, Insulin-Dependent | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0041296 | Tuberculosis | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0023467 | Leukemia, Myelocytic, Acute | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0400966 | Non-alcoholic Fatty Liver Disease | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0027873 | Neuromyelitis Optica | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0005398 | Cholestasis, Extrahepatic | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0025322 | Premature Menopause | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0010054 | Coronary Arteriosclerosis | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C1856058 | HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
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Last updated: August 19, 2024