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 |
---|---|---|---|---|---|
C0022610 | Kernicterus | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0007570 | Celiac Disease | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0007097 | Carcinoma | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C1337013 | Differentiated Thyroid Gland Carcinoma | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0600139 | Prostate carcinoma | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C1306459 | Primary malignant neoplasm | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0270210 | Lucey-Driscoll syndrome (disorder) | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C1704272 | Benign Prostatic Hyperplasia | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0011991 | Diarrhea | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0021400 | Influenza | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0376358 | Malignant neoplasm of prostate | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0023895 | Liver diseases | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0678222 | Breast Carcinoma | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0002875 | Cooley's anemia | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0003873 | Rheumatoid Arthritis | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0011226 | Hepatitis D Infection | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0699791 | Stomach Carcinoma | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0010414 | Infection by Cryptococcus neoformans | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C1562113 | Fleck corneal dystrophy | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0017205 | Gaucher Disease | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0008370 | Cholestasis | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0268138 | Xeroderma Pigmentosum, Complementation Group D | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0699889 | Malignant Female Reproductive System Neoplasm | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C2931132 | Crigler Najjar syndrome, type 2 | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
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Last updated: August 19, 2024