RBGP1 Polyclonal Antibody, 20ul Cryopreservation Loss of function mutations in

Loss of function mutations in SLC16A2 are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes

CDC42 is a member of the Rho GTPase family that regulates multiple cellular activities

and also Usher syndrome 1J (USH1J)

5 specifications available: 0

RBGP1 Polyclonal Antibody, 20ul Cryopreservation Loss of function mutations inMay act as a GTPase activating protein of RAB6A. May play a role in microtubule nucleation by centrosome. May participate in a RAB6A mediated pathway involved in the metaphase anaphase transition.,sequence Contaminating sequence. Potential poly A sequence.,sequence Intron retention.,Contains 1 PID domain.,Contains 1 Rab GAP TBC domain.,subcellular location: Predominantly cytosolic but also associated with the centrosome.,subunit: Interacts with RAB6A