FB2024_03 , released June 25, 2024
Allele: Dmel\CalpB505
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General Information
Symbol
Dmel\CalpB505
Species
D. melanogaster
Name
FlyBase ID
FBal0283066
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Cytology
Description

Imprecise excision of the progenitor insertion, resulting in a 1047bp deletion that removes the first 873bp of the CalpB coding sequence.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
Additional Information
Statement
Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 0 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 0 )
Disease
Interaction
References
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

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.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhanced by
NOT Enhanced by
Suppressed by
Statement
Reference
NOT suppressed by
Statement
Reference
Enhancer of
Additional Comments
Genetic Interactions
Statement
Reference

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.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Comments

CalpB+t5.6 rescues the border follicle cell migration defects of CalpB505 females.

Images (0)
Mutant
Wild-type
Stocks (0)
Availability

Stated to be lost.

Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (1)