As a result of the deletion the frame is changed after E740.
154bp deletion, resulting in a frameshift which is predicted to add 16 novel amino acids after residue 740. Nucleotide substitution: G5549A (silent polymorphism).
Location of a 154bp deletion beginning in codon G741, which leads to a frameshift and early translation termination. The resulting predicted protein has 16 novel amino acids added after residue 740.
cystoblast (with aubHN2)
2% of eggs from homozygous mothers are fertilized and embryos lack abdominal segments and pole cells, i.e. show a classic posterior group mutant phenotype.
aub[+]/aubN11 is an enhancer of abnormal meiotic cell cycle phenotype of RanGAPSd
aubHN2/aubN11 is a non-suppressor of abnormal eye color phenotype of wRNAi.GMR
aubHN2/aubN11 is a suppressor of primordial germ cell | ectopic phenotype of oskshort.bcd
aubN11 is a suppressor of phenotype of oskbcd.3UTR.Tag:polyHis
The segregation distortion seen in males carrying either the SD-5 or SD-Mad-ltcn Dp(2;2)RanGAPSD chromosome variant is enhanced (the k[[c]] value, or proportion of Dp(2;2)RanGAPSD-bearing progeny as the fraction of total progeny (corrected for viability), is significantly increased) if the males are also carrying a single copy of aubN11.
The yellowish eye colour caused by expression of one copy of wdsRNA.GMR in a wild-type background is not altered if the flies are also carrying aubHN2/aubN11.
Ectopic pole cells are not produced at the anterior of embryos derived from aubN11/aubHN ; oskshort.bcd females.