PDGFR-beta(Phospho Tyr771) Polyclonal Antibody, 20ul Centrifuges Mutations in this gene cause

Mutations in this gene cause primary ciliary dyskinesia type 3| as well as Kartagener syndrome| which are both diseases due to ciliary defects

See ZFP93 (MIM 604749) for additional information on zinc finger proteins

The protein encoded by this gene catalyzes the formation of 5-oxoproline from gamma-glutamyl dipeptides

This protein is very similar to the family member hnRPH

PDGFR-beta(Phospho Tyr771) Polyclonal Antibody, 20ul Centrifuges Mutations in this gene causeThis gene encodes a cell surface tyrosine kinase receptor for members of the platelet derived growth factor family. These growth factors are mitogens for cells of mesenchymal origin. The identity of the growth factor bound to a receptor monomer determines whether the functional receptor is a homodimer or a heterodimer, composed of both platelet derived growth factor receptor alpha and beta polypeptides. This gene is flanked on chromosome 5 by the