CC14C Polyclonal Antibody, 20ul High Speed Micro-Centrifuges Defects in this gene are

Defects in this gene are a cause of Zellweger syndrome (ZWS)

Mutations in this gene are associated with erythrocytosis familial type 4

the leucine-rich nuclear export signal receptor CRM1/Xpo1

and may be involved in the regulation of genes associated with activation and/or differentiation of macrophages

forming a highly conserved transcription factor that binds to CCAAT motifs in the promoter regions in a variety of genes

CC14C Polyclonal Antibody, 20ul High Speed Micro-Centrifuges Defects in this gene areDual specificity phosphatase. Preferentially dephosphorylates proteins modified by proline directed kinases (By similarity).