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

This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity

The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription

in the conversion of tyrosine to melanin

Polymorphisms in this gene are associated with susceptibility to gastric cancers

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.