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 42601 - 42625 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C2931132 Crigler Najjar syndrome, type 2 UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0036341 Schizophrenia UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0036572 Seizures UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0011226 Hepatitis D Infection UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C1337013 Differentiated Thyroid Gland Carcinoma UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C1306459 Primary malignant neoplasm UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0011860 Diabetes Mellitus, Non-Insulin-Dependent UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0152013 Adenocarcinoma of lung (disorder) UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0346647 Malignant neoplasm of pancreas UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0004096 Asthma UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0032580 Adenomatous Polyposis Coli UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0002895 Anemia, Sickle Cell UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0020433 Hyperbilirubinemia UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0334294 Multiple adenomatous polyps UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0271979 Thalassemia Intermedia UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0376358 Malignant neoplasm of prostate UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0010414 Infection by Cryptococcus neoformans UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0005283 beta Thalassemia UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0027651 Neoplasms UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0600139 Prostate carcinoma UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0524620 Metabolic Syndrome X UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0017205 Gaucher Disease UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0268138 Xeroderma Pigmentosum, Complementation Group D UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0006826 Malignant Neoplasms UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0342751 Generalized glycogen storage disease of infants UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503

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