FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\CtsL1llcnbw38
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General Information
Symbol
Dmel\CtsL1llcnbw38
Species
D. melanogaster
Name
FlyBase ID
FBal0091867
Feature type
allele
Associated gene
Dmel\CtsL1
Associated Insertion(s)
Carried in Construct
Also Known As
Cp1llcnbw38
Key Links
Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    CtsL150C
    (Gray et al., 1998)
    Cytology
    Description

    Deletion of approximately 2400bp rightwards from the P{CaSpeR} insertion in Cp150C.

    (Gray et al., 1998)
    Mutations Mapped to the Genome
    Curation Data
    Type
    Location
    Additional Notes
    References
    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 ( 1 )
        Disease
        Interaction
        References
        ameliorates  retinal degeneration
        modeled by norpAEE5
        (Kinser and Dolph, 2012)
        Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
         
        Disease-implicated variant(s)
         
        Phenotypic Data
        Phenotypic Class
        Phenotype Manifest In
        Detailed Description
        Statement
        Reference

        Cp1llcnbw38 mutants do not exhibit retinal degeneration when exposed to six days of constant light.

        (Kinser and Dolph, 2012)

        One copy of Cp1llcnbw38 is unable to suppress position effect variegation (PEV) at the w locus caused by In(1)wm4.

        One copy of Cp1llcnbw38 is unable to suppress the telomeric position effect (TPE) in stocks carrying a variegating P{hsp26-pt-T}39C-5 insertion at the telomere of the left arm of chromosome two.

        (Doheny et al., 2008)
        External Data
        Interactions
        Show genetic interaction network for Enhancers & Suppressors
        Phenotypic Class
        Phenotype Manifest In
        Suppressor of
        Statement
        Reference

        CtsL1llcnbw38 is a suppressor of eye phenotype of norpAEE5

        (Kinser and Dolph, 2012)

        CtsL1llcnbw38 is a suppressor of rhabdomere phenotype of norpAEE5

        (Kinser and Dolph, 2012)

        CtsL1llcnbw38 is a suppressor of ommatidium phenotype of norpAEE5

        (Kinser and Dolph, 2012)
        Additional Comments
        Genetic Interactions
        Statement
        Reference

        A Cp1llcnbw38 mutant background rescues the eye degeneration seen in norpA7 mutants exposed to six days constant light.

        (Kinser and Dolph, 2012)
        Xenogenetic Interactions
        Statement
        Reference
        Complementation and Rescue Data
        Complements

        Su(z)25

        (Doheny et al., 2008)
        Fails to complement

        CtsL1unspecified

        (Gray et al., 1998)
        Comments
        Images (0)
        Mutant
        Wild-type
        Stocks (2)
        Notes on Origin
        Discoverer
        External Crossreferences and Linkouts ( 0 )
        Synonyms and Secondary IDs (3)
        Reported As
        Symbol Synonym
        Cp1llcnbw38
        (Lyons et al., 2014, Kinser and Dolph, 2012, Doheny et al., 2008)
        CtsL1llcnbw38
        Df(2R)50C-llcnbw38
        (Gray et al., 1998)
        Name Synonyms
        Secondary FlyBase IDs
          References (4)