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

Mutations in this gene are associated with acromesomelic dysplasia

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

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

ABCB5 belongs to the ATP-binding cassette (ABC) transporter superfamily of integral membrane proteins

FIR Polyclonal Antibody, 50ul Primary Antibodies Mutations in this gene areFARP2 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