DFNA5 Polyclonal Antibody, 100ul Drug Development and Evaluation a disorder characterized by severely

a disorder characterized by severely reduced brain size and mental retardation

which are stem-loop structures found in the 5' UTR of ferritin mRNA

The protein encoded by this gene belongs to the Ser/Thr protein kinase family| and PIM subfamily

VRK3 (vaccinia related kinase 3) encodes a member of the vaccinia-related kinase (VRK) family of serine/threonine protein kinases

Belongs to the SMAGP family

DFNA5 Polyclonal Antibody, 100ul Drug Development and Evaluation a disorder characterized by severelyHearing impairment is a heterogeneous condition with over 40 loci described. Non syndromic hearing impairment protein 5 encoded by DFNA5 is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.