“…and Sirt5 have been implicated in phenotypes such as recovery from nutritional restriction and food deprivation [59][60][61][62]. Another group of genes including Rab3gap1, Cntn6, Dld, Dlg2, Grm5, Hmox2, Accn1, Cntnap2, Hpse2, Il1rapl2, Immp2l, Kalrn and Park2 are associated with neurological diseases such as autism, speech disorder and craniofacial abnormalities [63 -75].…”