FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\β-Specunspecified
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General Information
Symbol
Dmel\β-Specunspecified
Species
D. melanogaster
Name
FlyBase ID
FBal0212999
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

    The progeny of neuroblasts NB 3-5 and NB 7-3 show mostly normal axonal projections in stage 16 mutant embryos. However, axons have abnormal varicosities and additional small ectopic side branches. Alterations in the structure of the growth cones are seen; they appear enlarged with sometimes extensive, filopodia-like processes.

    Fas2-positive axons occasionally cross the midline in β-Specunspecified stage 16 embryos.

    Mutant larvae often fail to hatch. Newly hatched larvae initially crawl, eat and respond to touch, but grow increasingly sluggish over time, fail to grow and eventually die.

    Commissures appear to be of uneven thickness in stage 13 embryos and the RP1 neurons appear closer to the midline than normal. Some commissural axons directly turn to cross the midline again, instead of projecting further laterally to grow along the forming longitudinal tracts, resulting in a "circling axon" phenotype. The longitudinal connectives do not form properly. A small set of normally ipsilateral axons project contralaterally in mutant embryos.

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

    Fas2-positive axons occasionally cross the midline in β-Specunspecified stage 16 embryos. The frequency of this phenotype is enhanced if they also carry sliB1-32/+.

    Some axons can cross the midline in communspecified kusunspecified double mutant embryos, but in most neuromeres the comm mutant phenotype is epistatic to the kus mutant phenotype. However, if commissural axons have crossed the midline, then this neuromere shows a kus mutant phenotype.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    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
    kusunspecified
    β-Specunspecified
    Name Synonyms
    Secondary FlyBase IDs
    • FBal0117936
    • FBal0095345
    References (4)