FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
Allele: Dmel\rstD
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General Information
Symbol
Dmel\rstD
Species
D. melanogaster
Name
FlyBase ID
FBal0046384
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Mutagen
    Nature of the Allele
    Mutagen
    Progenitor genotype
    Cytology
    Description
    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

    Persistent larval salivary glands are found in 34% of rstD homozygotes, compared to 0% of controls, at 24 hours APF. These persistent salivary glands have large vacuoles, indicating that the normal cell death process has been arrested at an early stage.

    Mutants have slightly reduced eyes with a dark red colour, glassy texture and flattened appearance. The posterior and ventral border of the eye are abnormally straight. The number and relative position of photoreceptors is normal in the adult, but their general organisation is somewhat disturbed, with rare malrotated ommatidia. The pigment distribution around the ommatidia is also abnormal, being completely absent in some regions. No obvious misrouting of axonal fibres crossing the inner and outer optic chiasm are apparent in the optic lobe. The onset of programmed cell death is delayed in mutants, In wild-type cell death is seen between 25% and 35% pupal development (p.d.), but in mutants cell death is not seen until 35% p.d.. Maximal cell death is seen at 45% p.d. and is still observed by 50% p.d. and is only seen to be absent by 60% p.d. In mutants secondary and tertiary pigment cell fates do not differentiate properly.

    Reduced eyes with a glassy appearance, severity of the phenotype depends on the genetic background. Optic lobe has mild axonal pathfinding defects. Ommatidial structure is grossly disorganised due to lack of recognisable secondary and tertiary pigment cells.

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

    rstD has eye phenotype, suppressible by BacA\p35GMR.PH

    NOT suppressed by
    Statement
    Reference

    rstD has ommatidium phenotype, non-suppressible by BacA\p35GMR.PH

    Additional Comments
    Genetic Interactions
    Statement
    Reference

    The addition of to BacA\p35GMR.PH animals rescues the ventral-posterior 'cut' phenotype and the overall eye structure is somewhat improved, but the eye colouring and glassy appearance persist.

    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 (1)
    Reported As
    Symbol Synonym
    Name Synonyms
    Secondary FlyBase IDs
      References (4)