PDE7A Polyclonal Antibody, 50ul Plasmid Preparation Mutations in this gene are

Mutations in this gene are a cause of type 2E pseudohypoaldosteronism

The encoded protein forms a complex of alpha-1

Mutations in this gene are responsible for juvenile-onset vitelliform macular dystrophy (VMD2)

where it may control skin color variation and act as a determinant of brown or blue eye color

PDE7A Polyclonal Antibody, 50ul Plasmid Preparation Mutations in this gene areThe protein encoded by this gene belongs to the cyclic nucleotide phosphodiesterase (PDE) family, and PDE7 subfamily. This PDE hydrolyzes the second messenger, cAMP, which is a regulator and mediator of a number of cellular responses to extracellular signals. Thus, by regulating the cellular concentration of cAMP, this protein plays a key role in many important physiological processes. Alternatively spliced transcript variants encoding different