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
Displaying entries 42576 - 42600 of 62743 in total
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