GRSF1 Rabbit Polyclonal Antibody, 50ul Cell Biology Mutations in this gene are

Mutations in this gene are the cause of protein Z deficiency

consisting of KRTHB1

Knockout studies in mice suggested the roles of this gene in differentiation of T helper 2 (Th2) cells

an autosomal recessive disorder with cerebellar hypoplasia as a leading feature

PDCD2L (Programmed Cell Death 2 Like) is a Protein Coding gene

GRSF1 Rabbit Polyclonal Antibody, 50ul Cell Biology Mutations in this gene areThe protein encoded by this gene is a cellular protein that binds RNAs containing the G rich element. The protein is localized in the cytoplasm and has been shown to stimulate translation of viral mRNAs in vitro. Multiple transcript variants encoding different isoforms have been found for this gene.