SRp40 Polyclonal Antibody, 20ul miRNA / siRNA Synthesis Mutations in this gene cause

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

An important paralog of this gene is REG3G

Leydig cell adenoma with precocious puberty

Part of the postsynaptic scaffold in neuronal cells

A sulfated form of cholecystokinin-8 may modulate neuronal activity in the brain

SRp40 Polyclonal Antibody, 20ul miRNA / siRNA Synthesis Mutations in this gene causeThe protein encoded by SRSF5 (serine and arginine rich splicing factor 5) is a member of the serine arginine (SR) rich family of pre mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an RNA recognition motif (RRM) for binding RNA and an RS domain for binding other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition