Homozygous mutant follicle stem cell clones are present at a much lower frequency than control clones at 14 days (6% vs 46%) after clone induction.
Homozygous somatic clones produce bald patches in the notum missing microchaetae and can produce wing margin defects.
The RP2 motoneuron duplicated at the expense of the RP2sib. The aCC motoneuron is duplicated at the expense of the pCC interneuron. The Usib fates are duplicated at the expense of the U neurons. The dMP2 is duplicated at the expense of the vMP2. No change was observable in EL cell fate. This phenotype is the reciprocal of that shown for numb mutants. Mutant embryos show excess neuroblast formation characteristic of neurogenic mutants.
No effect on the faf eye phenotype.
Embryonic CNS exhibits severe disturbances and larval exhibit severe cuticle loss.
Severe "abruptex" phenotype. Capable of rescuing the lethality conferred by all negatively complementing Ax heteroallelic combinations, individuals display an Ax, not wild type, phenotype.
Weak embryonic neurogenic phenotype.
The phenotype of excess follicle stem cell progeny in between egg chambers that is caused by expression of hhhs.PI using heat shock twice daily for 3 days followed by a 3 day "chase" is dominantly suppressed by mam10, such that the number of inappropriate cells between egg chambers is strongly reduced.
There is no detectable dominant interaction with sno71e3.
Autosomal repressor.