Nucleotide substitution: C?T.
Base change CGC->TGC.
Fmr1R115C.EP3517 carries both the P{EP} insertion present in the progenitor allele and the amino acid replacement in the Fmr1 coding region.
Amino acid replacement: R115C.
C10105872T
C?T
R115C | Fmr1-PA; R115C | Fmr1-PB; R115C | Fmr1-PC; R115C | Fmr1-PD; R77C | Fmr1-PE; R77C | Fmr1-PF; R163C | Fmr1-PG; R163C | Fmr1-PH; R77C | Fmr1-PI; R115C | Fmr1-PJ; R115C | Fmr1-PK
R115C
LNv neuron (with Fmr1Δ113M)
Transheterozygosity to Fmr1Δ113Mresults in a defasciculation phenotype of the termini of the LNv neuron's dorsal projections.
Selected as: A mutation that suppresses the lethality caused when a Scer\GAL4 driver is used to overexpress Fmr1 from the P{EP}Fmr1EP3517 insertion.