FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Girdinunspecified
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General Information
Symbol
Dmel\Girdinunspecified
Species
D. melanogaster
Name
FlyBase ID
FBal0247334
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

    Homozygous embryos derived from females containing homozygous germline clones show defects in head morphogenesis and loss of anterior structures such as mouth hooks. The embryos have dorsal closure defects: the leading edge of the lateral epidermis has an exaggerated wavy appearance at the onset of dorsal closure, the dorsal-ventral polarisation of the migrating lateral epidermis cells is delayed compared to wild type, and the leading edge cells show impaired actin accumulation. The dorsal trunk of the tracheal tree is fragmented. Some of the embryos have an opening in the ectoderm on their ventral side. Some ectodermal cells in contact with the amnioserosa detach from the neighbouring tissue. Ectopic cysts of cells are seen just below the epidermis from stage 10 onwards, and they are abundant in stage 13 and later embryonic stages. These cysts appear to originate from fragmentation of the overlying epidermis.

    Expression of GirdindsRNA.Scer\UAS using Scer\GAL4en-e16E results in reduction of the posterior wing area and a decrease in cell size. These phenotypes are enhanced in a Girdinunspecified/+ background.

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

    Cuticle is almost completely absent in embryos that are zygotically mutant for shg and both maternally and zygotically mutant for Girdin.

    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 (2)
    Reported As
    Symbol Synonym
    Girdinunspecified
    Name Synonyms
    Secondary FlyBase IDs
      References (3)