RBGP1 Polyclonal Antibody, 50ul Gene Synthesis Mutations in this gene are

Mutations in this gene are associated with metaphyseal anadysplasia

It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides

Multiple transcript variants encoding different isoforms have been found for PER3

This intronless gene is deleted in AMME contiguous gene syndrome and may be involved in the cardiac and neurologic abnormalities found in the AMME contiguous gene syndrome

miscellaneous:Two forms have been identified in animal cells

RBGP1 Polyclonal Antibody, 50ul Gene Synthesis Mutations in this gene areMay 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