FIR Polyclonal Antibody, 50ul Primary Antibodies Mutations in this gene cause

Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome

Aberrant expression of this protein is associated with the growth and progression of certain tumors

Neuronal PAS domain-containing protein 2 encoded by NPAS2 is a member of the basic helix-loop-helix (bHLH)-PAS family of transcription factors

and has been linked to primary microcephaly and Alzheimer's disease

IQ calmodulin-binding motif-containing protein 1 has a central coiled-coil region and two calmodulin-binding IQ domains

FIR Polyclonal Antibody, 50ul Primary Antibodies Mutations in this gene causeFARP2 is a Protein Coding gene. FERM RhoGEF and pleckstrin domain containing protein 2 functions as guanine nucleotide exchange factor that activates RAC1. May have relatively low activity. Plays a role in the response to class 3 semaphorins and remodeling of the actin cytoskeleton. Plays a role in TNFSF11 mediated osteoclast differentiation, especially in podosome rearrangement and reorganization of the actin cytoskeleton. Regulates the activation of