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

which is involved in regulating the adenine nucleotide composition within a cell by catalyzing the reversible transfer of phosphate groups among adenine nucleotides

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

It regulates expression of the insulin gene

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