RBPJL Polyclonal Antibody, 100ul Antibodies Mutations in this gene cause

Mutations in this gene cause mitochondrial complex I deficiency

Mutations in ITCH are a cause of syndromic multisystem autoimmune disease

It has Catalytic activity for class I and II ArfGAPs in vitro

and heterodimerizes with a 28 kDa protein to form interleukin 27 (IL-27)

RBPJL Polyclonal Antibody, 100ul Antibodies Mutations in this gene causeThis gene encodes a member of the suppressor of hairless protein family. A similar protein in mouse is a transcription factor that binds to DNA sequences almost identical to that bound by the Notch receptor signaling pathway transcription factor recombining binding protein J. The mouse protein has been shown to activate transcription in concert with Epstein Barr virus nuclear antigen 2. Alternative splicing results in multiple transcript variants.