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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID ▲ | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0346647 | Malignant neoplasm of pancreas | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0024623 | Malignant neoplasm of stomach | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0085584 | Encephalopathies | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0279671 | Cervical Squamous Cell Carcinoma | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C4551686 | Malignant neoplasm of soft tissue | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0002395 | Alzheimer's Disease | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0005684 | Malignant neoplasm of urinary bladder | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0700639 | Pyloric Stenosis, Hypertrophic | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0028754 | Obesity | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C3553270 | DIARRHEA 6 | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C1857276 | Trichohepatoenteric Syndrome | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0278803 | Adenocarcinoma of small intestine | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0014544 | Epilepsy | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0008370 | Cholestasis | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0270210 | Lucey-Driscoll syndrome (disorder) | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0678222 | Breast Carcinoma | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0010324 | Crigler Najjar syndrome, type 1 | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0008350 | Cholelithiasis | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0857007 | Hyperbilirubinemia, Neonatal | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0002875 | Cooley's anemia | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0017551 | Gilbert Disease (disorder) | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0235974 | Pancreatic carcinoma | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0027947 | Neutropenia | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0947622 | Cholecystolithiasis | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0023530 | Leukopenia | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
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Last updated: August 19, 2024