CaMKIV Polyclonal Antibody, 50ul sgRNA customized design Mutations in this gene have

Mutations in this gene have been associated with congenital insensitivity to pain

This gene encodes the human homolog of the mouse p (pink-eyed dilution) gene

Mutations in this gene cause spinocerebellar ataxia type 15| a disease associated with an heterogeneous group of cerebellar disorders

the encoded protein is involved in the regulation of cell adhesion and migration

This cytokine is expressed in B cell lineage cells

CaMKIV Polyclonal Antibody, 50ul sgRNA customized design Mutations in this gene haveThe product of CAMK4 (calcium calmodulin dependent protein kinase IV) belongs to the serine threonine protein kinase family, and to the Ca(2+) calmodulin dependent protein kinase subfamily. This enzyme is a multifunctional serine threonine protein kinase with limited tissue distribution, that has been implicated in transcriptional regulation in lymphocytes, neurons and male germ cells.