CEA16 Polyclonal Antibody, 20ul Plasma Mutations in this gene cause

Mutations in this gene cause nocturnal frontal lobe epilepsy type 1

2008 [PubMed 18799455])

The protein encoded by this gene lacks the zinc binding activity of other family members

IKZF3 encodes a member of the Ikaros family of zinc-finger proteins

CEA16 Polyclonal Antibody, 20ul Plasma Mutations in this gene causeThe protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non syndromic autosomal dominant hearing loss.