FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\wrapperunspecified
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General Information
Symbol
Dmel\wrapperunspecified
Species
D. melanogaster
Name
FlyBase ID
FBal0094260
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

    Approximately half the midline glia cells die prematurely in homozygous embryos. In stage 14 homozygous embryos, the midline glia are in their correct final positions at the midline, as in wild-type embryos. By stage 15, one or both commissures may still be incompletely covered and the midline glia have sent out no processes, in contrast to wild-type stage 15 embryos where the glia have completely covered the commissural axons at the midline and have sent out processes to enwrap the commissural axon bundles more ventrally. Lateral to the midline glia cells, the commissural axons in the region between the midline glial cells and the longitudinal tracts are uncovered dorsally in homozygous embryos, in contrast to wild-type where they are almost completely covered by stage 15. At stage 16, the commissural axons of the anterior or posterior commissures are not covered dorsally, owing to the absence of either the MGA or MGP midline glial cells, although the MGM cell is always present. The glial extensions of the midline glial cells in homozygous embryos do not completely enwrap the axon bundles and do not enwrap individual axons or send thin sheet-like processes into the core of the commissures to separate groups of axons, as is seen in wild-type embryos.

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Phenotype Manifest In
    Additional Comments
    Genetic Interactions
    Statement
    Reference

    The midline glia phenotype is not seen in wrapperunspecified Df(3L)H99 double mutant embryos; these embryos contain supernumerary midline glia as in Df(3L)H99 single mutant embryos.

    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
    wrapperunspecified
    Name Synonyms
    Secondary FlyBase IDs
      References (2)