FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\chicgdh-5
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General Information
Symbol
Dmel\chicgdh-5
Species
D. melanogaster
Name
FlyBase ID
FBal0034344
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Mutagen
    Nature of the Allele
    Mutagen
    Progenitor genotype
    Cytology
    Description
    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 do not have gaps in the pCC/MP2 pathway.

    Mutant embryos show defects in motor axon extension, including the ISNb branch.

    24% heterozygotes have ectopic wing crossveins.

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

    The abnormal midline crossing of axons seen in robo1 heterozygotes is suppressed if the embryos are also heterozygous for chicgdh-5.

    Xenogenetic Interactions
    Statement
    Reference

    Only 17% of hemisegments have gaps in the pCC/MP2 pathway in Khc::Ggal\MLCKKA.ftz chicgdh-5 double homozygous embryos.

    The frequency of motor neuron axon stalls seen in chicgdh-5 embryos is increased by Khc::Ggal\MLCKKA.ftz.

    Complementation and Rescue Data
    Comments
    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer
    Comments
    Comments

    A competitive inhibitor of wild type prolifin.

    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (3)
    Reported As
    Symbol Synonym
    chigdh-5
    chicgdh-5
    Name Synonyms
    Secondary FlyBase IDs
      References (4)