TKNK Rabbit Polyclonal Antibody, 100ul DNA Oligo Synthesis Mutations in this gene result

Mutations in this gene result in cataract congenital nuclear autosomal recessive type 2

Belongs to the TRIM/RBCC family

Mutations in this gene may contribute to the congenital central hypoventilation syndrome (CCHS) phenotype in rare cases

1N have been reported to detect mulitple forms

TKNK Rabbit Polyclonal Antibody, 100ul DNA Oligo Synthesis Mutations in this gene resultThis gene encodes a member of the tachykinin family of secreted neuropeptides. The encoded preproprotein is proteolytically processed to generate the mature peptide which is primarily expressed in the central and peripheral nervous systems and functions as a neurotransmitter. This peptide is the ligand for the neurokinin 3 receptor. This protein is also expressed in the outer syncytiotrophoblast of the placenta and may be associated with pregnancy