Nucleotide substitution: A?C.
Amino acid replacement: V411G.
Base change CAG->CCG and GTG->GGG.
Nucleotide substitution: T?G.
Fmr1Q378P.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: Q378P.
T10104657G
T?G
V414G | Fmr1-PA; V404G | Fmr1-PB; V411G | Fmr1-PC; V411G | Fmr1-PD; V373G | Fmr1-PE; V376G | Fmr1-PF; V459G | Fmr1-PG; V452G | Fmr1-PH; V369G | Fmr1-PI; V411G | Fmr1-PJ; V411G | Fmr1-PK
V411G
One of two missense mutations in allele.
A10104756C
A?C
Q381P | Fmr1-PA; Q371P | Fmr1-PB; Q378P | Fmr1-PC; Q378P | Fmr1-PD; Q340P | Fmr1-PE; Q343P | Fmr1-PF; Q426P | Fmr1-PG; Q419P | Fmr1-PH; Q336P | Fmr1-PI; Q378P | Fmr1-PJ; Q378P | Fmr1-PK
Q378P
One of two missense mutations in allele.
Overexpression of Fmr1Q378P.EP3517 by Scer\GAL4P2.4.Pdf results in a defect in defasciculation 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.