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 61251 - 61275 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C1704272 Benign Prostatic Hyperplasia UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0011860 Diabetes Mellitus, Non-Insulin-Dependent UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0011991 Diarrhea UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0021400 Influenza UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0376358 Malignant neoplasm of prostate UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0023895 Liver diseases UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0678222 Breast Carcinoma UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0002875 Cooley's anemia UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0003873 Rheumatoid Arthritis UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0011226 Hepatitis D Infection UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0699791 Stomach Carcinoma UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0010414 Infection by Cryptococcus neoformans UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C1562113 Fleck corneal dystrophy UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0017205 Gaucher Disease UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0008370 Cholestasis UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0268138 Xeroderma Pigmentosum, Complementation Group D UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0699889 Malignant Female Reproductive System Neoplasm UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C2931132 Crigler Najjar syndrome, type 2 UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0018790 Cardiac Arrest UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0400966 Non-alcoholic Fatty Liver Disease UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0600139 Prostate carcinoma UGT1A5 54579 UDP glucuronosyltransferase family 1 member A5 P35504
C0008350 Cholelithiasis UGT1A5 54579 UDP glucuronosyltransferase family 1 member A5 P35504
C0524620 Metabolic Syndrome X UGT1A5 54579 UDP glucuronosyltransferase family 1 member A5 P35504
C0010324 Crigler Najjar syndrome, type 1 UGT1A5 54579 UDP glucuronosyltransferase family 1 member A5 P35504
C0017205 Gaucher Disease UGT1A5 54579 UDP glucuronosyltransferase family 1 member A5 P35504

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