Fmr1E68K.EP3517.X24 carries both the P{EP} insertion present in the progenitor allele and the amino acid replacement (base change GAG->AAG) in the Fmr1 coding region. Also has a second hit at 6056 changing from G to T without changing the encoded amino acid.
Amino acid replacement: E68K.
Nucleotide substitution: G?A.
Nucleotide substitution: G6056T.
A mutation that suppresses the lethality caused when a Scer\GAL4 driver is used to overexpress Fmr1 from the P{EP}Fmr1EP3517 insertion.
Separable from: P{EP}Fmr1EP3517.