SMPX Rabbit Polyclonal Antibody, 100ul Antibodies Mutations in this gene have

Mutations in this gene have been associated with an elevated risk for a variety of diseases and disorders

this domain interacts with the SMRT/N-CoR-mSin3A HDAC complex and is directly involved in repressing and silencing gene transcription

Mutations in this gene have been associated with cylindromatosis| multiple familial trichoepithelioma| and Brooke-Spiegler syndrome

MAP3K2/MEKK2

This protein prevents hemolytic anemia from oxidative stress by stabilizing hemoglobin

SMPX Rabbit Polyclonal Antibody, 100ul Antibodies Mutations in this gene haveThis gene encodes a small protein that has no known functional domains. Mutations in this gene are a cause of X linked deafness 4 and the encoded protein may play a role in the maintenance of inner ear cells subjected to mechanical stress. Alternatively spliced transcript variants have been observed for this gene.