FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\kstunspecified
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General Information
Symbol
Dmel\kstunspecified
Species
D. melanogaster
Name
FlyBase ID
FBal0101350
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    Cytology
    Description

    FlyBase curator comment: this entry is used to capture phenotypic information when the particular allele (or allele combination) used by the author could not be determined but the context of the experiment suggests that the phenotype being described is some kind of loss of function.

    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

    Nuclei are often mispositioned in cuprophilic cells in the midgut of mutant third instar larvae, with 13-71% of the nuclei in each gut being found at the outer edges of the cuprophilic cells, causing a bulge near the pore. Pore size is normal in the mutant cuprophilic cells.

    The gut lumen is acidified in mutant first instar larvae. However, mutant third instar larvae show a statistically significant decrease in overall gut acidification compared to controls.

    Mutant wing cells produce normal-looking hairs, but the hairs are often found on a small pedestal. The wing cell surface that is not hair is rough and remnants of cell outlines are sometimes visible.

    The border cells migrate ahead of the follicle cell monolayer in 73% of mutant egg chambers, in contrast to wild-type where the border cells and follicle cell monolayer migrate in a concerted fashion. Egg chambers where the border cells are retarded relative to the follicle cells are occasionally seen. Most mutant oocytes occupy a larger portion of the egg chamber than in wild type during follicle cell migration, while the oocyte shows no significant overgrowth at the completion of migration. Most mutant oocytes occupy a larger portion of the egg chamber than in wild type during border cell migration. Some follicle cells often remain in contact with the nurse cell membranes at stage 10A. These follicle cells still attempt to make the appropriate adhesive contacts with the oocyte membrane, pulling the oocyte membrane towards them and grossly distorting the nurse cells/oocyte interface. In most cases, the subsequent inward migration of the follicle cell layer at stage 10B proceeds relatively normally, but in rare, extreme cases, the centripetally migrating cells penetrate between nearby nurse cell membranes and cause one or more nurse cells to become included within the egg along with the oocyte. Mutant follicle cells often appear more cuboidal than wild-type follicle cells. There is no overproliferation in the follicle monolayer. The majority of follicle cells fail to constrict their apices over the oocyte as they migrate, in contrast to wild type. The mean apical surface area of mutant follicle cells is almost twice that of wild type. Comparison of the apical surface areas of mutant follicle cells in chambers during migration with those where migration has been completed reveals a slight increase, suggesting that the monolayer cannot withstand the forces exerted by the growing oocyte (in addition to the constriction defect). In approximately 10% of egg chambers, migratory cells that are well separated from, or trail behind, the main border cell cluster are seen.

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Phenotype Manifest In
    NOT Enhancer of
    Statement
    Reference

    kst[+]/kstunspecified is a non-enhancer of mitotic domain 1 | embryonic cycle 14 phenotype of CycB+t10

    NOT Suppressor of
    Statement
    Reference

    kst[+]/kstunspecified is a non-suppressor of mitotic domain 1 | embryonic cycle 14 phenotype of CycB+t10

    Additional Comments
    Genetic Interactions
    Statement
    Reference
    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
    kstunspecified
    Name Synonyms
    Secondary FlyBase IDs
      References (5)