Nucleotide substitution: C?T.
Amino acid replacement: Q276term.
Fmr1Q276Stop.EP3517 carries both the P{EP} insertion present in the progenitor allele and the nonsense mutation in the Fmr1 coding region.
C10105203T
C?T
Q276term | Fmr1-PA; Q276term | Fmr1-PB; Q276term | Fmr1-PC; Q276term | Fmr1-PD; Q238term | Fmr1-PE; Q238term | Fmr1-PF; Q324term | Fmr1-PG; Q324term | Fmr1-PH; Q238term | Fmr1-PI; Q276term | Fmr1-PJ; Q276term | Fmr1-PK
Q276term
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.