MerTK/Tyro3(Phospho Tyr749/681) Polyclonal Antibody, 50ul Pathway and Network Analysis A rare microsatellite polymorphism in

A rare microsatellite polymorphism in this gene is associated with cancer in patients of varying radiosensitivity

three tropomyosin homology domains and an ATP/GTP binding site motif A

Diseases associated with CCR2 include idiopathic anterior uveitis and cd3zeta deficiency

The product of this gene is a member of the leucine-rich-repeat (LRR) superfamily of proteins

MerTK/Tyro3(Phospho Tyr749/681) Polyclonal Antibody, 50ul Pathway and Network Analysis A rare microsatellite polymorphism inThis gene is a member of the MER AXL TYRO3 receptor kinase family and encodes a transmembrane protein with two fibronectin type III domains, two Ig like C2 type (immunoglobulin like) domains, and one tyrosine kinase domain. Mutations in this gene have been associated with disruption of the retinal pigment epithelium (RPE) phagocytosis pathway and onset of autosomal recessive retinitis pigmentosa (RP).