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 61001 - 61025 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0002878 Anemia, Hemolytic UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0007102 Malignant tumor of colon UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0038362 Stomatitis UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0947622 Cholecystolithiasis UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C1337013 Differentiated Thyroid Gland Carcinoma UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0010054 Coronary Arteriosclerosis UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0600139 Prostate carcinoma UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0262584 Carcinoma, Small Cell UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0149925 Small cell carcinoma of lung UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C1458155 Mammary Neoplasms UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0153594 Malignant neoplasm of testis UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C1266194 Lymphocyte Rich Classical Hodgkin Lymphoma UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0007107 Malignant neoplasm of larynx UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0268138 Xeroderma Pigmentosum, Complementation Group D UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0524620 Metabolic Syndrome X UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0279000 Liver and Intrahepatic Biliary Tract Carcinoma UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0595989 Carcinoma of larynx UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0007137 Squamous cell carcinoma UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0684249 Carcinoma of lung UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C1140680 Malignant neoplasm of ovary UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0685938 Malignant neoplasm of gastrointestinal tract UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0342751 Generalized glycogen storage disease of infants UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0008370 Cholestasis UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0023449 Acute lymphocytic leukemia UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309
C0023895 Liver diseases UGT1A1 54658 UDP glucuronosyltransferase family 1 member A1 P22309

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Last updated: August 19, 2024