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 |
---|---|---|---|---|---|
C0038362 | Stomatitis | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0947622 | Cholecystolithiasis | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C1337013 | Differentiated Thyroid Gland Carcinoma | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0010054 | Coronary Arteriosclerosis | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0600139 | Prostate carcinoma | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0262584 | Carcinoma, Small Cell | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0149925 | Small cell carcinoma of lung | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C1458155 | Mammary Neoplasms | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0153594 | Malignant neoplasm of testis | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C1266194 | Lymphocyte Rich Classical Hodgkin Lymphoma | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0007107 | Malignant neoplasm of larynx | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0268138 | Xeroderma Pigmentosum, Complementation Group D | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0524620 | Metabolic Syndrome X | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0595989 | Carcinoma of larynx | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0007137 | Squamous cell carcinoma | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0684249 | Carcinoma of lung | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C1140680 | Malignant neoplasm of ovary | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0685938 | Malignant neoplasm of gastrointestinal tract | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0342751 | Generalized glycogen storage disease of infants | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0008370 | Cholestasis | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0023449 | Acute lymphocytic leukemia | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0023895 | Liver diseases | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0036572 | Seizures | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0002875 | Cooley's anemia | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
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Last updated: August 19, 2024