Nucleotide substitution: C?T.
Amino acid replacement: Q327term.
Fmr1Q327Stop.EP3517 carries both the P{EP} insertion present in the progenitor allele and the nonsense mutation in the Fmr1 coding region.
C10104992T
C?T
Q330term | Fmr1-PA; Q327term | Fmr1-PC; Q327term | Fmr1-PD; Q289term | Fmr1-PE; Q292term | Fmr1-PF; Q375term | Fmr1-PG; Q327term | Fmr1-PJ; Q327term | Fmr1-PK
Q327term
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.