FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\ksrS-548
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General Information
Symbol
Dmel\ksrS-548
Species
D. melanogaster
Name
FlyBase ID
FBal0049699
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Mutagen
    Nature of the Allele
    Mutagen
    Progenitor genotype
    Cytology
    Description

    4bp substitution that changes two consecutive amino acids in the N-terminus of the protein. Amino acid replacement: L50S. Amino acid replacement: R51G.

    Mutations Mapped to the Genome
    Curation Data
    Type
    Location
    Additional Notes
    References
    Amino acid change:

    L50S|ksr-PA

    Amino acid change:

    R51G|ksr-PA

    Reported amino acid change:

    L50S

    Reported amino acid change:

    R51G

    Comment:

    A 4bp substitution that changes two consecutive amino acids. The amino acid changes are L50S and R51G.

    Inserted_sequence:

    AGTG

    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

    Few ommatidia contain the normal complement of receptor cells.

    Homozygotes are subviable and have rough eyes.

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Suppressed by
    Statement
    Reference

    ksrS-548 has visible phenotype, suppressible by ttk190.1

    ksrS-548 has visible phenotype, suppressible by aopyan-XE18

    Phenotype Manifest In
    Suppressed by
    Statement
    Reference

    ksrS-548 has eye phenotype, suppressible by PTP-ERXE-3022

    ksrS-548 has ommatidium phenotype, suppressible by PTP-ERXE-3022

    ksrS-548 has eye phenotype, suppressible by PTP-ERXE-2776

    ksrS-548 has ommatidium phenotype, suppressible by PTP-ERXE-2776

    Suppressor of
    Statement
    Reference

    ksrS-548 is a suppressor of eye phenotype of Ras85DV12.sev

    Additional Comments
    Genetic Interactions
    Statement
    Reference

    Heterozygous PTP-ERXE-3022, PTP-ERXE-2776 as well as deficiency alleles of PTP-ER suppress the rough eyes and loss of photoreceptor cells seen in homozygous ksrS-548.

    Up to 99% ommatidia are wild type in a aopyan-XE18 or ttk190.1 mutant background.

    Dominantly suppresses the rough eye phenotype of Ras85DV12.sev.

    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 (3)
    Reported As
    Symbol Synonym
    ksrS-548
    Name Synonyms
    Secondary FlyBase IDs
      References (3)