MY18A Polyclonal Antibody, 100ul Metabolic enzymes tool compounds Defects in TMEM237 are a

Defects in TMEM237 are a cause of Joubert syndrome-14

It is a cytoskeletal protein that interacts with F-actin and Arp2/3 complex and plays an important role in regulation of actin assembly and cytoskeleton dynamics

GPR37L1 (G Protein-Coupled Receptor 37 Like 1) is a Protein Coding gene

Enhance the versatility of your MX-S and MX-F Vortex Mixers with the VT1

MY18A Polyclonal Antibody, 100ul Metabolic enzymes tool compounds Defects in TMEM237 are aThe TIAF1 protein is coded in the 3' UTR region of MYO18A.,May be involved in the maintenance of the stromal cell architectures required for cell to cell contact.,Contains 1 IQ domain.,Contains 1 myosin head like domain.,Contains 1 PDZ (DHR) domain.,subcellular location: Colocalizes with actin.,subcellular location: Lacks the PDZ domain. Diffusely localized in the cytoplasm.,subunit: Homodimer. Interacts with JAK3 and actin.,