FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\ptcC.UAS
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General Information
Symbol
Dmel\ptcC.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0124965
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

UASt sequences drove expression of ptc that has had amino acids 9 to 676 deleted.

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 ( 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

Expression of ptcC.Scer\UAS when driven by Scer\GAL471B or Scer\GAL469B causes no detectable wing phenotype. Expression of both ptcN.Scer\UAS and ptcC.Scer\UAS when driven by Scer\GAL471B causes both mild and severe wing phenotypes in the wing - partial fusion of wing veins 3 and 4 to the deletion of the region between veins 2 and 4. Expression of both ptcN.Scer\UAS and either ptcC.Scer\UAS when driven by Scer\GAL4en-e16E leads to a drastic loss of central wing pattern.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

The addition of both ptcN.Scer\UAS and ptcC.Scer\UAS (when driven by Scer\GAL4da.G32) to ptc16 embryos complements the cuticle defects of these embryos - instead of 20% of embryos having a "ptc" phenotype, only 1% do. (with ptcN.Scer\UAS) Partially rescues: ptc16

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
Comments
Comments

Carried in a plasmid and transfected into S2 cells for co-immunoprecipitation experiments.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
ptcC.Scer\UAS
ptcC.UAS
Name Synonyms
Secondary FlyBase IDs
    References (1)