AR26L Rabbit Polyclonal Antibody, 20ul Roller Bottles Defects in this gene are

Defects in this gene are a cause of deafness autosomal recessive type 49 (DFNB49)

cts as one of several non-catalytic accessory components of the cytoplasmic dynein 1 complex that are thought to be involved in linking dynein to cargos and to adapter proteins that regulate dynein function

CBFA2T3 is also a putative breast tumor suppressor

Expansion of a 20 amino acid polyalanine tract in this protein by 5-13 aa has been associated with congenital central hypoventilation syndrome

These cell surface lectins are characterized by structural motifs in the immunoglobulin (Ig)-like domains and sialic acid recognition sites in the first Ig V set domain

AR26L Rabbit Polyclonal Antibody, 20ul Roller Bottles Defects in this gene are