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DisGeNET
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 |
|---|---|---|---|---|---|
| C0009806 | Constipation | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0005695 | Bladder Neoplasm | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0524620 | Metabolic Syndrome X | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0002895 | Anemia, Sickle Cell | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0345904 | Malignant neoplasm of liver | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0021400 | Influenza | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C2239176 | Liver carcinoma | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0030567 | Parkinson Disease | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0600139 | Prostate carcinoma | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0038356 | Stomach Neoplasms | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C1565662 | Acute Kidney Insufficiency | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0009402 | Colorectal Carcinoma | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0017205 | Gaucher Disease | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0699790 | Colon Carcinoma | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0011991 | Diarrhea | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0028754 | Obesity | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0017921 | Glycogen storage disease type II | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0007131 | Non-Small Cell Lung Carcinoma | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C2609414 | Acute kidney injury | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0279606 | Childhood Hepatocellular Carcinoma | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0006142 | Malignant neoplasm of breast | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0007102 | Malignant tumor of colon | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0010414 | Infection by Cryptococcus neoformans | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0342751 | Generalized glycogen storage disease of infants | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0014544 | Epilepsy | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
