FB2026_02 , released June 18, 2026
Allele: Dmel\Pcyt1EP831
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General Information
Symbol
Dmel\Pcyt1EP831
Species
D. melanogaster
Name
FlyBase ID
FBal0131724
Feature type
allele
Associated gene
Dmel\Pcyt1
Associated Insertion(s)
P{EP}Pcyt1EP831
Carried in Construct
Key Links
Genomic Maps

Allele class

hypomorphic allele - genetic evidence

Mutagen
Nature of the Allele
Allele class

hypomorphic allele - genetic evidence

(Weber et al., 2003)
Mutagen
P-element activity
(Gene Disruption Project members, 2001-)
Progenitor genotype
Associated Insertion(s)
P{EP}Pcyt1EP831
Cytology
Description
Allele components
Component
Use(s)
Inserted element
P{EP}
Regulatory region(s)
UAS
Mutations Mapped to the Genome
Curation Data
Variant Molecular Consequences
Associated Sequence Data
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
 
UniProtKB/Swiss-Prot
    UniProtKB/TrEMBL
      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

      Cct116919/Cct1EP831 transheterozygotes display a rough eye phenotype; eyes have defects in ommatidial rotation and a reduced number of photoreceptor cells.

      (Weber et al., 2003)
      External Data
      Interactions
      Show genetic interaction network for Enhancers & Suppressors
      Phenotypic Class
      Phenotype Manifest In
      Suppressor of
      Statement
      Reference

      Cct1[+]/Pcyt1EP831 is a suppressor of crossvein | increased number phenotype of EgfrE3

      (Weber et al., 2003)
      Additional Comments
      Genetic Interactions
      Statement
      Reference

      Cct1EP831/+, EgfrE3/+ double mutants suppress the ectopic wing vein phenotype seen at the tip of L2 in single EgfrE3/+ mutants.

      (Weber et al., 2003)
      Xenogenetic Interactions
      Statement
      Reference
      Complementation and Rescue Data
      Rescued by

      Pcyt1EP831 is rescued by Pcyt1+t11.2

      (Weber et al., 2003)
      Comments
      Images (0)
      Mutant
      Wild-type
      Stocks (0)
      Notes on Origin
      Discoverer
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (4)
      Reported As
      Symbol Synonym
      CG1049EP831
      Cct1EP0831
      (Weber et al., 2003)
      Cct1EP831
      Pcyt1EP831
      Name Synonyms
      Secondary FlyBase IDs
        References (2)