FB2024_04 , released June 25, 2024
Allele: Dmel\sogYL26
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General Information
Symbol
Dmel\sogYL26
Species
D. melanogaster
Name
FlyBase ID
FBal0046503
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

    Only 31% of sogP129D/sogYL26 flies survive to adulthood. Of these, 15% exhibit partial loss of the posterior crossvein and the rest show more subtle alterations in which the posterior crossvein appears as a fragmented line.

    Double mutants of dppH48 with sogYL26 or sog1 have phenotypes identical to that of the dpp mutant alone.

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

    sogYL26/sogP129D is a suppressor of crossvein phenotype of tokΔ2-41/tokE1

    sog[+]/sogYL26 is a suppressor | partially of crossvein phenotype of tokΔ2-41/tokE1

    Additional Comments
    Genetic Interactions
    Statement
    Reference

    sogYL26/+; tokΔ2-41/tokE1 escapers exhibit partial posterior crossveins with significantly more crossvein material than tokΔ2-41/tokE1 escapers. Further, crossveins are almost completely restored in sogYL26/sogP129D; tokΔ2-41/tokE1 animals.

    Extra copies of dpp enhance the mutant phenotype causing profound alterations in the cuticular pattern of the neurogenic ectoderm.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments

    sogT:Ivir\HA1 rescues sogYL26 and sogYL26/sogU2 mutants to viable and fertile adults.

    sog+mPa rescues sogYL26 and sogYL26/sogU2 mutants to viable and fertile adults.

    Images (0)
    Mutant
    Wild-type
    Stocks (1)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (1)
    Reported As
    Symbol Synonym
    Name Synonyms
    Secondary FlyBase IDs
      References (6)