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 54376 - 54400 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0271979 Thalassemia Intermedia UGT1A9 54600 UDP glucuronosyltransferase family 1 member A9 O60656
C0023895 Liver diseases UGT1A9 54600 UDP glucuronosyltransferase family 1 member A9 O60656
C0024535 Malaria, Falciparum UGT1A9 54600 UDP glucuronosyltransferase family 1 member A9 O60656
C0857007 Hyperbilirubinemia, Neonatal UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0010324 Crigler Najjar syndrome, type 1 UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C1337013 Differentiated Thyroid Gland Carcinoma UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0008350 Cholelithiasis UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0271979 Thalassemia Intermedia UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0270210 Lucey-Driscoll syndrome (disorder) UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0002875 Cooley's anemia UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0006826 Malignant Neoplasms UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0009402 Colorectal Carcinoma UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0002312 alpha-Thalassemia UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C1306459 Primary malignant neoplasm UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0600139 Prostate carcinoma UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0005684 Malignant neoplasm of urinary bladder UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0524620 Metabolic Syndrome X UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C2939465 Deficiency of glucose-6-phosphate dehydrogenase UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0017551 Gilbert Disease (disorder) UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0014859 Esophageal Neoplasms UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0011226 Hepatitis D Infection UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0023473 Myeloid Leukemia, Chronic UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0020433 Hyperbilirubinemia UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0376358 Malignant neoplasm of prostate UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0018790 Cardiac Arrest UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9

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