FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\pebX001
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General Information
Symbol
Dmel\pebX001
Species
D. melanogaster
Name
FlyBase ID
FBal0031500
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
hntXO01
Key Links
Genomic Maps

Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    Cytology
    Description

    Amino acid replacement: Q348term.

    The truncated protein produced is predicted to contain only 3 of the 14 zinc fingers present in the wild-type protein.

    Nucleotide substitution: C?T.

    Mutations Mapped to the Genome
    Curation Data
    Type
    Location
    Additional Notes
    References
    Nucleotide change:

    C4621326T

    Reported nucleotide change:

    C?T

    Amino acid change:

    Q348term | peb-PA; Q348term | peb-PB

    Reported amino acid change:

    Q348term

    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

    R3/R3 type symmetrical ommatidia (where the R3 or R4 cell has not taken up the correct position) are found at the borders of homozygous clones in the eye. In these ommatidia, either the R3 or R4 cell, or both, is mutant and the chirality of these ommatidia is sometimes also incorrect. Homozygous clones in the eye result in a scar. Mutant cells in larval eye discs show depletion or more diffuse localisation of F-actin, especially in the more posterior part of the mutant clone.

    84.4% of embryos exhibit a germband retraction phenotype, 12.3% a dorsal closure phenotype. 79% of embryos that complete germ band retraction exhibit an anterior-open or dorsal-hole phenotype characteristic of the failure of dorsal closure.

    Genetic mosaic embryos show phenotypes that reveal a correlation between the genotype of the amnioserosa and the success or failure of germ band retraction.

    Hemizygous embryos show weak failure of germband retraction. 68% have abdominal segment 6.5 or greater at the posterior tip. The head skeleton is abnormal.

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

    pebX001 has amnioserosa phenotype, non-suppressible by InRhs.PF

    Additional Comments
    Genetic Interactions
    Statement
    Reference

    Blocking amnioserosal cell death by making the mutant embryos also mutant for Df(3L)H99 does not alter the effect of mutant clones. InRhs.PF almost completely suppresses the germ band retraction defect of pebX001 embryos. The premature apoptosis of amnioserosa cells is not, however, rescued.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Rescued by
    Comments

    The failure of germband retraction can be rescued by pebhs.PY.

    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer
    Comments
    Comments

    Maternal germline clonal analysis demonstrates there is no maternal effect.

    l(1)EH275a is not allelic to peb; l(1)EH275a1 complements pebhnt-1, pebX001, pebEH704a and peb1.

    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (2)
    Reported As
    Name Synonyms
    Secondary FlyBase IDs
      References (5)