Imprecise excision of the progenitor insertion, resulting in a 1047bp deletion that removes the first 873bp of the CalpB coding sequence.
Homozygous and CalpB505/Df(3L)AC1 females show a delay in border follicle cell migration, with 32-38% of border cells failing to complete migration to the anterior end of the oocyte by stage 10. 46% of border cells show delay in the dorsal movement of border cells which is normally seen after they reach the oocyte.
CalpA808/Df(2R)ED3716, CalpB505 has viable phenotype
CalpA808/Df(2R)ED3716, CalpB505 has fertile phenotype
CalpB505 has border follicle cell phenotype, enhanceable by rheaNIG.6831R/Scer\GAL4slbo.2.6
CalpB505 has border follicle cell phenotype, enhanceable by ifNIG.9623R/Scer\GAL4slbo.2.6
CalpB505 has border follicle cell phenotype, enhanceable by mysNIG.1560R/Scer\GAL4slbo.2.6
CalpB505 has border follicle cell phenotype, non-enhanceable by CalpA808/Df(2R)ED3716
CalpB505 has border follicle cell phenotype, non-enhanceable by rheaR367A.H.UAS.GFP/Scer\GAL4slbo.2.6
CalpB505 has border follicle cell phenotype, suppressible by rheaH.UASp.mGFP6/Scer\GAL4slbo.2.6
CalpB505 has border follicle cell phenotype, non-suppressible by CalpA808/Df(2R)ED3716
CalpB505 has border follicle cell phenotype, non-suppressible by rheaR367A.H.UAS.GFP/Scer\GAL4slbo.2.6
CalpB505 is an enhancer of border follicle cell phenotype of Scer\GAL4slbo.2.6, rheaNIG.6831R
CalpB505 is an enhancer of border follicle cell phenotype of Scer\GAL4slbo.2.6, ifNIG.9623R
CalpB505 is an enhancer of border follicle cell phenotype of Scer\GAL4slbo.2.6, mysNIG.1560R
The delay in border follicle cell migration seen in CalpB505 females is unaffected if they are also carrying CalpA808/Df(2R)ED3716.
Females expressing rheaNIG.6831R under the control of Scer\GAL4slbo.2.6 in a CalpB505 background show an increase in the severity of the border follicle cell migration defect compared to either CalpB505 single mutants or females expressing rheaNIG.6831R under the control of Scer\GAL4slbo.2.6 in a wild-type background.
Females expressing ifNIG.9623R under the control of Scer\GAL4slbo.2.6 in a CalpB505 background show an increase in the severity of the border follicle cell migration defect compared to either CalpB505 single mutants or females expressing ifNIG.9623R under the control of Scer\GAL4slbo.2.6 in a wild-type background.
Females expressing mysNIG.1560R under the control of Scer\GAL4slbo.2.6 in a CalpB505 background show an increase in the severity of the border follicle cell migration defect compared to either CalpB505 single mutants or females expressing mysNIG.1560R under the control of Scer\GAL4slbo.2.6 in a wild-type background.
Expression of rheaH.Scer\UAS.T:Avic\GFP-m6 under the control of Scer\GAL4slbo.2.6 restores normal border follicle cell migration in CalpB505 females.
Expression of rheaR376A.H.Scer\UAS.T:Avic\GFP under the control of Scer\GAL4slbo.2.6 has no effect on the border follicle cell migration defects seen in CalpB505 females.
CalpB505 is rescued by CalpB+t5.6
CalpB+t5.6 rescues the border follicle cell migration defects of CalpB505 females.
Stated to be lost.