Nucleotide substitution: C?T.
Amino acid replacement: Q329term.
Fmr1Q329Stop.EP3517 carries both the P{EP} insertion present in the progenitor allele and the nonsense mutation in the Fmr1 coding region.
C10104986T
C?T
Q332term | Fmr1-PA; Q322term | Fmr1-PB; Q329term | Fmr1-PC; Q329term | Fmr1-PD; Q291term | Fmr1-PE; Q294term | Fmr1-PF; Q377term | Fmr1-PG; Q370term | Fmr1-PH; Q287term | Fmr1-PI; Q329term | Fmr1-PJ; Q329term | Fmr1-PK
Q329term
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.