VAPA Rabbit Polyclonal Antibody, 20ul PCR Series Defects in this gene are

Defects in this gene are a cause of dwarfism| while hypersecretion of the encoded protein is a cause of gigantism

This gene encodes a member of the inorganic phosphate transporter family

Though the canonical MOR belongs to the superfamily of 7-transmembrane-spanning G-protein-coupled receptors some isoforms of this gene have only 6 transmembrane domains

but the full-length nature of many of these variants has not been determined

It catalyzes the transformation of 3-cis and 3-trans-enoyl-CoA esters arising during the stepwise degradation of cis-

VAPA Rabbit Polyclonal Antibody, 20ul PCR Series Defects in this gene areThe protein encoded by this gene is a type IV membrane protein. It is present in the plasma membrane and intracellular vesicles. It may also be associated with the cytoskeleton. This protein may function in vesicle trafficking membrane fusion protein complex assembly and cell motility. Alternative splicing occurs at this locus and two transcript variants encoding distinct isoforms have been identified.