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 15151 - 15175 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0024117 Chronic Obstructive Airway Disease SIRT2 22933 sirtuin 2 Q8IXJ6
C0003864 Arthritis SIRT2 22933 sirtuin 2 Q8IXJ6
C0023486 Prolymphocytic Leukemia SIRT2 22933 sirtuin 2 Q8IXJ6
C0242379 Malignant neoplasm of lung SIRT2 22933 sirtuin 2 Q8IXJ6
C4551686 Malignant neoplasm of soft tissue SIRT2 22933 sirtuin 2 Q8IXJ6
C0007097 Carcinoma SIRT2 22933 sirtuin 2 Q8IXJ6
C0270952 Muscular Dystrophy, Oculopharyngeal SIRT2 22933 sirtuin 2 Q8IXJ6
C0034068 Pulmonary Eosinophilia SIRT2 22933 sirtuin 2 Q8IXJ6
C0035412 Rhabdomyosarcoma SIRT2 22933 sirtuin 2 Q8IXJ6
C0041234 Chagas Disease SIRT2 22933 sirtuin 2 Q8IXJ6
C4721610 Carcinoma, Ovarian Epithelial SIRT2 22933 sirtuin 2 Q8IXJ6
C1269683 Major Depressive Disorder SIRT2 22933 sirtuin 2 Q8IXJ6
C0015934 Fetal Growth Retardation SIRT2 22933 sirtuin 2 Q8IXJ6
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma SIRT2 22933 sirtuin 2 Q8IXJ6
C0005695 Bladder Neoplasm SIRT2 22933 sirtuin 2 Q8IXJ6
C0476089 Endometrial Carcinoma SIRT2 22933 sirtuin 2 Q8IXJ6
C4721806 Carcinoma, Basal Cell SIRT2 22933 sirtuin 2 Q8IXJ6
C0220668 Congenital contractural arachnodactyly SIRT2 22933 sirtuin 2 Q8IXJ6
C0004096 Asthma SIRT2 22933 sirtuin 2 Q8IXJ6
C0020456 Hyperglycemia SIRT2 22933 sirtuin 2 Q8IXJ6
C0497327 Dementia SIRT2 22933 sirtuin 2 Q8IXJ6
C0017152 Gastritis SIRT2 22933 sirtuin 2 Q8IXJ6
C0017636 Glioblastoma SIRT2 22933 sirtuin 2 Q8IXJ6
C0346647 Malignant neoplasm of pancreas SIRT2 22933 sirtuin 2 Q8IXJ6
C0340076 Asthmatic pulmonary eosinophilia SIRT2 22933 sirtuin 2 Q8IXJ6

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Last updated: August 19, 2024