The coordinate for the nucleotide substitution is the genomic sequence location.
Nucleotide substitution: T8901222A.
T8908122A
T8901222A
Y635term | mfr-PB; Y970term | mfr-PC; Y882term | mfr-PD; Y1178term | mfr-PF; Y970term | mfr-PI; Y179term | mfr-PJ
Y1216term
The mutations were reported relative to the longest mfr protein isoform, which uses an upstream ATG start relative to the annotated version in release 5.54.
female semi-sterile (with mfrZ4070)
male sterile (with Df(3L)ED4415)
male sterile (with Df(3L)hry-i22)
dorsal appendage (with Df(3L)hry-i22)
dorsal appendage (with mfrZ0695)
dorsal appendage (with mfrZ4070)
egg chamber (with Df(3L)hry-i22)
egg chamber (with mfrZ0695)
egg chamber (with mfrZ4070)
Approximately 20% of eggs laid by mfrZ1386/Df(3L)h-i22 females produce are abnormal. The defects are visible in late stage eggs as abnormally short and closely apposed dorsal appendages, signifying a ventralized egg chamber. mfrZ1386/mfrZ4070 and mfrZ0695/mfrZ1386 females also produce defective eggs with a penetrance of approximately 41% and 35% respectively.
Only 43% of the total eggs laid by mfrZ4070/mfrZ1386 females mated to wild-type males hatch. The hatch rate is similar between the eggs that have wild-type eggshell morphology and those with defective dorsal appendages. The mutant embryos show delayed development compared to controls.
Selected as: a male sterile mutation from the Zuker collection.