PAR-6Beta Polyclonal Antibody, 100ul Gene Synthesis Mutations in this gene are

Mutations in this gene are the cause of Wagner syndrome type 1

cyclic nucleotide phosphodiesterase (PDE) family

MIM 603908)

Latrophilins may function in both cell adhesion and signal transduction

Alternative splicing of EXO1 results in three transcript variants encoding two different isoforms

PAR-6Beta Polyclonal Antibody, 100ul Gene Synthesis Mutations in this gene arePARD6B is a member of the PAR6 family and encodes a protein with a PSD95 Discs large ZO1 (PDZ) domain, an OPR domain and a semi Cdc42 Rac interactive binding (CRIB) domain. This cytoplasmic protein is involved in asymmetrical cell division and cell polarization processes as a member of a multi protein complex.