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 |
---|---|---|---|---|---|
C0376358 | Malignant neoplasm of prostate | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0010414 | Infection by Cryptococcus neoformans | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0005283 | beta Thalassemia | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0027651 | Neoplasms | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0600139 | Prostate carcinoma | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0524620 | Metabolic Syndrome X | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0017205 | Gaucher Disease | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0268138 | Xeroderma Pigmentosum, Complementation Group D | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0006826 | Malignant Neoplasms | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0342751 | Generalized glycogen storage disease of infants | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0028754 | Obesity | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0023895 | Liver diseases | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0007097 | Carcinoma | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0017921 | Glycogen storage disease type II | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0021400 | Influenza | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0020433 | Hyperbilirubinemia | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0024623 | Malignant neoplasm of stomach | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0271979 | Thalassemia Intermedia | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0017921 | Glycogen storage disease type II | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0036572 | Seizures | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0023473 | Myeloid Leukemia, Chronic | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0017551 | Gilbert Disease (disorder) | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0010324 | Crigler Najjar syndrome, type 1 | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0039730 | Thalassemia | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0027947 | Neutropenia | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
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Last updated: August 19, 2024