FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\shdunspecified
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General Information
Symbol
Dmel\shdunspecified
Species
D. melanogaster
Name
FlyBase ID
FBal0086343
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

    Mutant embryos have alterations in embryonic morphology. No epidermal folds are found below the ventral nerve cord. Instead of stretching dorsally, the ectoderm appears to fold like an accordion in the anterior-posterior axis. As a consequence the gut is frequently pushed outside the embryo. By the end of embryogenesis the ventral folding of the epidermis pushes the ventral nerve cord further deep into the embryo. Beside the dorsal closure phenotypes, defects are also seen during head involution and in gut morphology. Mutant embryos also typically have fused commissure phenotypes where anterior and posterior commissures are not separated. Longitudinal connectives are very close to the midline, and frequent midline crossing can be seen from the inner most axon bundles can be seen. Glial cell organisation is severely affected in mutants. Glial cells do not cover the entirity of connectives, but appear to avoid the medial most axon tracts. Mutants have a significant increase in the number of midline glial cells. An average of almost 5 are seen per neuromere.

    In mutant embryos, commissures are fused but connectives are not affected. Embryos show a compacted phenotype with the dorsal edges remaining open for much longer than wild type. Dorsal closure does happen in the end. The PNS often shows defasciculating axons and an increase in the number of sensory neurons.

    shdunspecified mutant embryos show no differentiation of the cuticle or head skeleton.

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Phenotype Manifest In
    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
    shdunspecified
    Name Synonyms
    Secondary FlyBase IDs
      References (4)