UASt regulatory sequences drive expression of the Fmr1 coding region (amplified from the LD09557 cDNA), carrying both a G269E substitution in the KH1 domain and a I307N substitution in the KH2 domain. These changes are equivalent to a G266E change and a I304N change respectively in the orthologous human FMR1 gene (each of these variants is associated with Fragile X Syndrome). The coding sequence is tagged at the N-terminal end with EGFP.