c-Myc (Acetyl Lys148) Rabbit Polyclonal Antibody, 50ul Filtration Mutations in this gene are

Mutations in this gene are the cause of atrioventricular septal defect

This gene is a member of the AB hydrolase superfamily and encodes a protein with an alpha/beta hydrolase fold

It regulates expression of the insulin gene

The protein encoded by TMEM237 (transmembrane protein 237) is a tetraspanin protein that is thought to be involved in WNT signaling

it is expressed at high levels in peripheral blood leukocytes

c-Myc (Acetyl Lys148) Rabbit Polyclonal Antibody, 50ul Filtration Mutations in this gene aredisease: A chromosomal aberration involving MYC may be a cause of a form of B cell chronic lymphocytic leukemia. Translocation t(8; 12)(q24; q22) with BTG1. disease: Overexpression of MYC is implicated in the etiology of a variety of hematopoietic tumors. Participates in the regulation of gene transcription. Binds DNA both in a non specific manner and also specifically to recognizes the core sequence 5' CAC