BNIPL Polyclonal Antibody, 50ul Nucleic Acid Amplification It is a member of

It is a member of the MADS (MCM1

Mutations in this gene cause familial cold autoinflammatory syndrome type 2

Inhibition of myosin phosphatase leads to increased myosin phosphorylation and enhanced smooth muscle contraction

and cellular activation and has been linked to Gray platelet syndrome

This gene is one of several genes identified in a region of the X chromosome associated with an X-linked cleft palate (CPX) disorder

BNIPL Polyclonal Antibody, 50ul Nucleic Acid Amplification It is a member ofThe protein encoded by this gene interacts with several other proteins, such as BCL2, ARHGAP1, MIF and GFER. It may function as a bridge molecule between BCL2 and ARHGAP1 CDC42 in promoting cell death. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.