PRKRA Polyclonal Antibody, 100ul Recombinant Protein Mutations in this gene can

Mutations in this gene can cause Charcot-Marie-Tooth disease type 4H (CMT4H)| a disorder of the peripheral nervous system

The function of this protein has not been identified

Read-through transcription exists between this gene and the upstream homeobox A10 (HOXA10) gene

Defects in this gene cause Hailey-Hailey disease

q21) is associated with familial clear cell renal cancer

PRKRA Polyclonal Antibody, 100ul Recombinant Protein Mutations in this gene canThis gene encodes a protein kinase activated by double stranded RNA which mediates the effects of interferon in response to viral infection. Mutations in this gene have been associated with dystonia. Alternative splicing results in multiple transcript variants.