PAR-3 Polyclonal Antibody, 100ul RNA Tools Mutations in this gene cause

Mutations in this gene cause autosomal dominant severe congenital neutropenia

fatty acids and bilirubin

craniofacial anomalies

tissue specificity:Heart and brain

MIM 601625) transfer ADP-ribose from NAD+ to the target protein

PAR-3 Polyclonal Antibody, 100ul RNA Tools Mutations in this gene causeF2RL2 encodes a member of the protease activated receptor (PAR) family which is a subfamily of the seven transmembrane G protein coupled cell surface receptor family. The coagulation factor II thrombin receptor like 2 acts as a cofactor in the thrombin mediated cleavage and activation of the protease activated receptor family member PAR4. The encoded protein plays an essential role in hemostasis and thrombosis. Alternate splicing results in multiple