PNKD Polyclonal Antibody, 50ul Recombinant Protein Mutations in this gene have

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly

and are activated at distinct physiological temperatures

unlike MDM2 which degrades p53

Because of the conservation of N protein sequence and its strong immunogenicity

and regulation of autophagy

PNKD Polyclonal Antibody, 50ul Recombinant Protein Mutations in this gene haveThis gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants.