{"symbol":"PREPL","synonyms":["CMS22"],"name":"prolyl endopeptidase-like","description":"The protein encoded by this gene belongs to the prolyl oligopeptidase subfamily of serine peptidases. Mutations in this gene have been associated with hypotonia-cystinuria syndrome, also known as the 2p21 deletion syndrome. Several alternatively spliced transcript variants encoding either the same or different isoforms have been described for this gene.[provided by RefSeq, Jan 2010]","ncbiEntrezGeneId":9581,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/9581","proteins":[{"symbol":"PPCEL_HUMAN","href":"/api/1.0/protein/PPCEL_HUMAN"}],"hgncRootFamilies":[]}