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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 |
|---|---|---|---|---|---|
| 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 |
| 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 |
