MNX1 Polyclonal Antibody, 50ul Sealing Film The chromosome 22 breakpoint for

The chromosome 22 breakpoint for this translocation is located within the BCR gene (BCR

The gene spans 29 kb containing 13 exons

The members of this family are ubiquitously expressed and are generally most abundant in mitochondria-enriched tissues such as heart

|PTM:While translation occurs| the particular unfolded structure after the GRR repeat promotes the generation of p52 making it an acceptable substrate for the proteasome

MNX1 Polyclonal Antibody, 50ul Sealing Film The chromosome 22 breakpoint forThis gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.