The GSN gene (GSN stands for Gelsolin) is a protein-coding gene located on chromosome 9q33.2.
The protein encoded by this gene, Gelsolin, binds to the "plus" (or barbed) ends of actin monomers and filaments to prevent monomer exchange (end-blocking or capping). The protein, which is regulated by calcium, can promote the assembly of monomers into filaments (nucleation) and separate already formed filaments (Nag S et al. 2009). Several transcript variants have been found for this gene, encoding several different isoforms.
Defects in this gene are a cause of familial amyloidosis of the Finnish type (AGel amyloidosis/FAF). The signaling pathways involved include the innate immune system and apoptotic cleavage of cellular proteins.