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 ▼ |
---|---|---|---|---|---|
C0162557 | Liver Failure, Acute | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0041327 | Tuberculosis, Pulmonary | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0236664 | Alcohol-Related Disorders | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0011570 | Mental Depression | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0280324 | Laryngeal Squamous Cell Carcinoma | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0005684 | Malignant neoplasm of urinary bladder | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0027439 | Nasopharyngeal Neoplasms | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0003850 | Arteriosclerosis | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0024302 | Reticulosarcoma | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0302592 | Cervix carcinoma | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0030567 | Parkinson Disease | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0009324 | Ulcerative Colitis | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0162309 | Adrenoleukodystrophy | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0235833 | Congenital diaphragmatic hernia | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0024121 | Lung Neoplasms | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0030305 | Pancreatitis | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C4048158 | Convulsions | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0004096 | Asthma | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0267952 | Fibrosis of pancreas | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0205644 | Carcinoma, Granular Cell | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C1621958 | Glioblastoma Multiforme | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0017154 | Gastritis, Atrophic | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0017638 | Glioma | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0023452 | Childhood Acute Lymphoblastic Leukemia | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0751606 | Adult Acute Lymphocytic Leukemia | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
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Last updated: August 19, 2024