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 10651 - 10675 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0585442 Osteosarcoma of bone SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C1332979 Childhood Lymphoma SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0020456 Hyperglycemia SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0025267 Multiple Endocrine Neoplasia Type 1 SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0007787 Transient Ischemic Attack SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0340305 Inferior Wall Myocardial Infarction SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C1332206 Adult Lymphoma SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0027051 Myocardial Infarction SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C2239176 Liver carcinoma SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0878544 Cardiomyopathies SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C1868683 B-CELL MALIGNANCY, LOW-GRADE SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0949857 Mitochondrial Respiratory Chain Deficiencies SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C1856127 Bile acid synthesis defect, congenital, 2 AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0019158 Hepatitis AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0011849 Diabetes Mellitus AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0000768 Congenital Abnormality AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0019159 Hepatitis A AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0392514 Hereditary hemochromatosis AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0029456 Osteoporosis AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0023895 Liver diseases AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0024523 Malabsorption Syndrome AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0027051 Myocardial Infarction AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0008372 Intrahepatic Cholestasis AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0005779 Blood Coagulation Disorders AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C2711227 Steatohepatitis AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857

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Last updated: August 19, 2024