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 |
---|---|---|---|---|---|
C0007103 | Malignant neoplasm of endometrium | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0685938 | Malignant neoplasm of gastrointestinal tract | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0008370 | Cholestasis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0005283 | beta Thalassemia | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0019829 | Hodgkin Disease | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0022354 | Jaundice, Obstructive | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0005695 | Bladder Neoplasm | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0400966 | Non-alcoholic Fatty Liver Disease | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0019196 | Hepatitis C | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0280324 | Laryngeal Squamous Cell Carcinoma | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0017154 | Gastritis, Atrophic | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0018418 | Gynecomastia | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0024121 | Lung Neoplasms | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0524620 | Metabolic Syndrome X | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0023473 | Myeloid Leukemia, Chronic | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0678222 | Breast Carcinoma | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0085669 | Acute leukemia | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0038325 | Stevens-Johnson Syndrome | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0010346 | Crohn Disease | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0042870 | Vitamin D Deficiency | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C1565489 | Renal Insufficiency | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0007789 | Cerebral Palsy | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C1561643 | Chronic Kidney Diseases | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0026769 | Multiple Sclerosis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
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Last updated: August 19, 2024