RGS16(Phospho Tyr168) Polyclonal Antibody, 50ul NGS Oligos Defects in MEF2A could be

Defects in MEF2A could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

suggesting that this gene is a tumor suppressor candidate

Recruits TRAF3 and DISC1 to the microtubules

The encoded protein may play a role in the control of craniofacial patterning and the differentiation and survival of inhibitory neurons in the forebrain

E3 ubiquitin-protein ligase Mdm2 can promote tumor formation by targeting tumor suppressor proteins

RGS16(Phospho Tyr168) Polyclonal Antibody, 50ul NGS Oligos Defects in MEF2A could beThe protein encoded by this gene belongs to the 'regulator of G protein signaling' family. It inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits. It also may play a role in regulating the kinetics of signaling in the phototransduction cascade.