Amino acid replacement: M146V.
A20433475G
M168V | Psn-PA; M168V | Psn-PB; M168V | Psn-PC; M168V | Psn-PD; M168V | Psn-PE
Analogous M146V mutation in human PSEN1 implicated in Alzheimer's disease 3; mutation carried on in vitro construct; site of nucleotide substitution in fly gene inferred by FlyBase curator based on reported amino acid change.
Flies carrying two copies of PsnM146V.Scer\UAS expressed under the control of Scer\GAL4GMR.PF have a weak rough eye phenotype. Flies carrying two copies of Psn+14.Scer\UAS expressed under the control of Scer\GAL4GMR.PF have a rough eye phenotype, which is enhanced if the flies are also carrying one copy of PsnM146V.Scer\UAS.
Scer\GAL4GMR.PF/PsnM146V.UAS is an enhancer of visible phenotype of rprGMR.PH
Scer\GAL4GMR.PF/PsnM146V.UAS is an enhancer of eye phenotype of rprGMR.PH
Weakly enhances the eye phenotype of flies expressing rprGMR.PH when expressed under the control of Scer\GAL4GMR.PF.
Carried in a plasmid and transfected into S2 cells to study the effect of Psn protein on N protein processing.