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 10626 - 10650 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0011581 Depressive disorder SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0039585 Androgen-Insensitivity Syndrome SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0023903 Liver neoplasms SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0009324 Ulcerative Colitis SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0028945 oligodendroglioma SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C3714756 Intellectual Disability SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0264766 Rheumatic mitral stenosis SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0014173 Endometrial Hyperplasia SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C1175175 Severe Acute Respiratory Syndrome SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0033578 Prostatic Neoplasms SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0011854 Diabetes Mellitus, Insulin-Dependent SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0021390 Inflammatory Bowel Diseases SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C1332629 Breast Fibrocystic Change, Proliferative Type SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0699791 Stomach Carcinoma SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0524620 Metabolic Syndrome X SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0038013 Ankylosing spondylitis SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0400966 Non-alcoholic Fatty Liver Disease SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0025517 Metabolic Diseases SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0007222 Cardiovascular Diseases SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0008350 Cholelithiasis SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C1860787 DOWN SYNDROME CRITICAL REGION SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C1332986 Childhood Osteosarcoma SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0010051 Coronary Aneurysm SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0019187 Hepatitis, Alcoholic SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0015397 Disorder of eye SULT1E1 6783 sulfotransferase family 1E member 1 P49888

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Last updated: August 19, 2024