Amino acid replacement: R695term.
C15841580T
R696term | spn-E-PA
R695term
The mutaiton was reported as R695@. There is no R at position 695 in the reference sequence. The closest R residues are at 694 and 696. The mutation was mapped to R696. It isn't possible to create a stop with a single nucleotide change for R694 (CGT). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
egg (with spn-Ehls-Δ125)
oocyte (with spn-Ehls-Δ157)
The eggs laid by spn-E4E2-14/spn-Ehls-Δ125 mutant females exhibit severe dorsoventral patterning defects, with a high percentage of collapsed eggs or eggs with no dorsal appendages.
spn-Ehls-Δ157/spn-E4E2-14 oocytes have thick microtubule bundles and rapid cytoplasmic movement.