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 2701 - 2725 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0002965 Angina, Unstable SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0677886 Epithelial ovarian cancer SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0035309 Retinal Diseases SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C1704436 Peripheral Arterial Diseases SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0025149 Medulloblastoma SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0023434 Chronic Lymphocytic Leukemia SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0025362 Mental Retardation SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0595989 Carcinoma of larynx SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0026269 Mitral Valve Stenosis SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0024809 Marijuana Abuse SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0007102 Malignant tumor of colon SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0039685 Tetralogy of Fallot SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0701818 Choledocholithiasis SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0015306 Hereditary Multiple Exostoses SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0018801 Heart failure SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0009402 Colorectal Carcinoma SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0007124 Noninfiltrating Intraductal Carcinoma SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0032460 Polycystic Ovary Syndrome SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0277528 Traveler's diarrhea SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0919267 ovarian neoplasm SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0010068 Coronary heart disease SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0015674 Chronic Fatigue Syndrome SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0276496 Familial Alzheimer Disease (FAD) SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0027533 Neck Neoplasms SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0011581 Depressive disorder SULT1E1 6783 sulfotransferase family 1E member 1 P49888

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Last updated: August 19, 2024