FB2025_01 , released February 20, 2025
Allele: Dmel\capsID.UAS
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General Information
Symbol
Dmel\capsID.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0125100
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
UAS-CapsDN
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

UASt regulatory sequences drive expression of caps lacking the intracellular domain (encodes the amino terminal 470 amino acids of caps).

Allele components
Component
Use(s)
Encoded product / tool
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 ( 1 )
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

Ectopic expression of capsID.Scer\UAS, a construct lacking the intracellular part, in the developing eye, under the control of Scer\GAL4GMR.PF, display a mild R7 stopping phenotype.

Expression of capsID.Scer\UAS in both R7 and R8 photoreceptors, under the control of Scer\GAL4sev.PM181, generates a strong R7 axon stopping phenotype.

Expression of capsID.Scer\UAS in ventral muscle 12 causes synaptic terminal defects. In contrast, expression of capsID.Scer\UAS with Scer\GAL4elav.PLu in motoneurons does not lead to synaptic terminal abnormalities.

Embryos that express capsID.Scer\UAS under the control of Scer\GAL4twi.PG show normal development of the tracheal system.

Third instar larvae expressing capsID.Scer\UAS under the control of Scer\GAL4elav.PLu at 29oC show defects in the trajectory of the motorneurons that innervate muscle 12 in 19% of hemisegments. Expression of capsID.Scer\UAS under the control of Scer\GAL4how-24B does not result in an increased frequency of the terminals of motorneurons that normally innervate muscle 12 forming ectopic synapses on muscle 13.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhancer of
Suppressor of
Additional Comments
Genetic Interactions
Statement
Reference

All larvae co-expressing psqKK111691 and EgfrUAS.cBa under the control of Scer\GAL4ap-md544 during larval stages (using Gal80[ts] for the temporal regulation of expression) wing discs tumors, associated with higher numbers of myoblasts. These phenotypes are partially suppressed by the co-expression of capsID.UAS.

Expression of capsID.Scer\UAS under the control of Scer\GAL4twi.PG enhances the severity of the dorsal trunk defects of trn28.4 embryos.

capsID.Scer\UAS suppresses the loss of laterally located somatic clones of salmScer\UAS.cdCa; Scer\GAL4Act5C.PP cells in late third instar wing discs.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
capsID.Scer\UAS
capsID.UAS
Name Synonyms
Secondary FlyBase IDs
    References (9)