Nuclear envelope integral membrane protein 2 (NEMP2)

Nuclear envelope integral membrane protein 2 (NEMP2) is a protein encoded by the NEMP2 gene and localizes to the inner membrane of the nuclear envelope[1][2][3][9]. It is a predicted transmembrane protein believed to be involved in maintaining nuclear envelope structure and organization[2][3]. NEMP2 has been associated with certain genetic diseases, such as Hemochromatosis type 4 and cone-rod dystrophy 1, but there is limited evidence of its direct role as a therapeutic target or established biomarker[2]. No drugs are currently known to interact with this protein in a clinical context.

Other names

TMEM194BTransmembrane protein 194BUPF0571 transmembrane proteinNEMP2