IMMP2L (Inner Mitochondrial Membrane Peptidase Subunit 2) is a Protein Coding gene. Diseases associated with IMMP2L include Deafness, Autosomal Dominant 2A and Gilles De La Tourette Syndrome. Among its related pathways are Protein export. IMMP2L encodes a protein involved in processing the signal peptide sequences used to direct mitochondrial proteins to the mitochondria. The encoded protein resides in the mitochondria and is one of the necessary proteins for the catalytic activity of the mitochondrial inner membrane peptidase (IMP) complex. Two variants that encode the same protein have been described for IMMP2L.
