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 |
---|---|---|---|---|---|
C0002875 | Cooley's anemia | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0023530 | Leukopenia | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0279607 | Adult Hepatocellular Carcinoma | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0020433 | Hyperbilirubinemia | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0010324 | Crigler Najjar syndrome, type 1 | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0009375 | Colonic Neoplasms | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0268138 | Xeroderma Pigmentosum, Complementation Group D | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0699885 | Carcinoma of bladder | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0005283 | beta Thalassemia | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0270210 | Lucey-Driscoll syndrome (disorder) | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0027947 | Neutropenia | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0017551 | Gilbert Disease (disorder) | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0005684 | Malignant neoplasm of urinary bladder | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0857007 | Hyperbilirubinemia, Neonatal | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0376358 | Malignant neoplasm of prostate | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0007097 | Carcinoma | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C2931132 | Crigler Najjar syndrome, type 2 | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0008350 | Cholelithiasis | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0007137 | Squamous cell carcinoma | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0947622 | Cholecystolithiasis | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C1306459 | Primary malignant neoplasm | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0013595 | Eczema | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0011226 | Hepatitis D Infection | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0013395 | Dyspepsia | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
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Last updated: August 19, 2024