{"symbol":"PMPCA","synonyms":["P-55","ALPHA-MPP","INPP5E"],"name":"peptidase (mitochondrial processing) alpha","description":"The protein encoded by this gene is found in the mitochondrion, where it represents the alpha subunit of a proteolytic heterodimer. This heterodimer is responsible for cleaving the transit peptide from nuclear-encoded mitochondrial proteins. Defects in this gene are a cause of spinocerebellar ataxia, autosomal recessive 2. [provided by RefSeq, Mar 2016]","ncbiEntrezGeneId":23203,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/23203","proteins":[{"symbol":"MPPA_HUMAN","href":"/api/1.0/protein/MPPA_HUMAN"}],"hgncRootFamilies":[]}