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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 ▼ |
|---|---|---|---|---|---|
| C0684249 | Carcinoma of lung | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0005283 | beta Thalassemia | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0002875 | Cooley's anemia | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0027651 | Neoplasms | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0013336 | Dwarfism | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0015934 | Fetal Growth Retardation | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0011991 | Diarrhea | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C1704436 | Peripheral Arterial Diseases | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0678222 | Breast Carcinoma | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0345904 | Malignant neoplasm of liver | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0006142 | Malignant neoplasm of breast | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0242379 | Malignant neoplasm of lung | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0023903 | Liver neoplasms | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0029182 | orbit (eye disorders) | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0345905 | Intrahepatic Cholangiocarcinoma | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0020501 | Primary Hyperoxaluria | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0027651 | Neoplasms | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0036572 | Seizures | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0006826 | Malignant Neoplasms | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0011615 | Dermatitis, Atopic | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| 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 |
