FB2024_03 , released June 25, 2024
Allele: Dmel\kuzH143
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General Information
Symbol
Dmel\kuzH143
Species
D. melanogaster
Name
FlyBase ID
FBal0082860
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
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    Mutations Mapped to the Genome
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    Variant Molecular Consequences
    Associated Sequence Data
    DNA sequence
    Protein sequence
     
    Expression Data
    Reporter Expression
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    Marker for
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    Human Disease Associations
    Disease Ontology (DO) Annotations
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    Modifiers Based on Experimental Evidence ( 0 )
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    Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
     
    Disease-implicated variant(s)
     
    Phenotypic Data
    Phenotypic Class
    Phenotype Manifest In
    Detailed Description
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    kuzH143 mutants exhibit thinning of the longitudinal connectives and thickening of the commissures compared to controls. 50% of the segments examined in kuzH143 homozygous mutants display FasII axon crossing defects. No FasII axon crossing defects are seen in kuzH143/+. However kuzH143 heterozygotes do exhibit mild ectopic ap neuron crossing.

    Homozygous clones induced in the thorax at 48-72 hours after egg laying are missing macrochaetae and microchaetae, and a tuft of macrochaetae develops in the area devoid of bristles. Homozygous clones induced in the dorsal part of the wing at 48-72 hours after egg laying give rise to thickening of the wing veins and nicks at the wing margin.

    External Data
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    Phenotypic Class
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    Enhancer of
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    NOT Enhancer of
    NOT Suppressor of
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    Phenotype Manifest In
    Enhanced by
    Statement
    Reference

    kuzH143 has commissure | embryonic stage 16 phenotype, enhanceable by sli2/sli[+]

    kuzH143 has commissure | embryonic stage 16 phenotype, enhanceable by robo[+]/sli[+]/robo15/sli1

    Enhancer of
    Statement
    Reference
    NOT Enhancer of
    NOT Suppressor of
    Additional Comments
    Genetic Interactions
    Statement
    Reference

    One copy each of sli1 and robo5 enhances the FasII axon midline crossing phenotype seen in kuzH143 stage 16 embryos.

    A kuzH143 background enhances the FasII midline crossing phenotype seen in sli1, robo5 transheterozygous stage 16 embryos.

    kuzH143, sli2 transheterozygous stage 16 embryos display a stronger ectopic ap neuron crossing phenotype than either mutant alone.

    Xenogenetic Interactions
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    Complementation and Rescue Data
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    Synonyms and Secondary IDs (1)
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      References (4)