FB2026_02 , released June 18, 2026
Allele: Dmel\CG13895190
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General Information
Symbol
Dmel\CG13895190
Species
D. melanogaster
Name
FlyBase ID
FBal0258666
Feature type
allele
Associated gene
Dmel\CG13895
Associated Insertion(s)
P{?SUPor-P}CG13895190
Carried in Construct
Key Links
Genomic Maps

Allele class
Mutagen
Nature of the Allele
Allele class
Mutagen
P-element activity
(Benchabane et al., 2011)
Progenitor genotype
P{SUPor-P}CG13895KG05495
(Benchabane et al., 2011)
Associated Insertion(s)
P{?SUPor-P}CG13895190
Cytology
Description

Imprecise excision of the progenitor insertion, resulting in a 8187bp deletion from +228 to +8414 relative to the CG13895 transcription start site. 5kb of the original insertion remains.

(Benchabane et al., 2011)
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
delins
3L:699,787..707,973 [-]
Comment:

8187 bp deletion resulting from the imprecise excision of P{SUPor-P}CG13895KG05495. Extends from +228 to +8414 relative to the CG13895 transcription start site. 3L:708201 (R5) was used as the transcription start site for the mapping. Approximately 5kb of the original insertion remains.

(Benchabane et al., 2011)
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
      External Data
      Interactions
      Show genetic interaction network for Enhancers & Suppressors
      Phenotypic Class
      Phenotype Manifest In
      Suppressor of
      Statement
      Reference

      CG13895190 is a suppressor of retina phenotype of ApcQ8

      (Benchabane et al., 2011)
      Additional Comments
      Genetic Interactions
      Statement
      Reference

      Homozygosity for CG13895190 partially suppresses the apoptosis of photoreceptor cells which is seen in ApcQ8 homozygotes; photoreceptors are seen only in a subset of ommatidia, and these ommatidia have less than seven photoreceptors.

      (Benchabane et al., 2011)
      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
      CG13895190
      (Benchabane et al., 2011)
      Df(3L)190
      (Benchabane et al., 2011)
      Name Synonyms
      Secondary FlyBase IDs
        References (1)