HMX2 Polyclonal Antibody, 20ul Polyclonal Antibodies CDC42 and RAC1

CDC42 and RAC1

An alternative splice variant has been described but its full length sequence has not been determined

PTM:Phosphorylated on tyrosine and serine/threonine

AKR1C3 shares high sequence identity with three other gene members and is clustered with those three genes at chromosome 10p15-p14

HMX2 Polyclonal Antibody, 20ul Polyclonal Antibodies CDC42 and RAC1The protein encoded by this gene is a member of the NKL homeobox family of transcription factors. Members in this family are of ancient origin and play an important role in organ development during embryogenesis. A related mouse protein plays a role in patterning of inner ear structures. In humans, variations in a region containing this gene have been associated with inner ear malformations, vestibular dysfunction, and hearing loss.