FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\sogY506
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General Information
Symbol
Dmel\sogY506
Species
D. melanogaster
Name
FlyBase ID
FBal0032753
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
sogYS06, sogSY06
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
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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
    Statement
    Reference

    Hemizygous embryos have a dorsalised cuticle containing extremely truncated denticles, a completely U-shaped body, herniated head and Filzkorper defects.

    Dorsalisation: Cuticles of sogY506 hemizygous embryos show reduction of the dorsal extent of the ventral denticle belts.

    A reduction in salivary gland placode is seen in these embryos. The anterior rows of denticle belts are not reduced in these mutants.

    sogY506/Y embryos are abnormally shaped due to a failure in germ band extension. The ventral denticle belts are reduced in size (the reduction is less severe than in brkM68/Y embryos). Defects are seen in the outer row of sna-expressing neuroblasts in the ventral neurogenic region. Only a small number of scattered amnioserosa cells are produced.

    Ventralized embryos: rings or patches of ventral denticles along dorsoventral axis. Disruption of germ band extension that leads to the invagination of posterior segments into the interior of the embryo.

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

    sogY506 is a suppressor of lethal phenotype of tld1/tld14

    Phenotype Manifest In
    Enhanced by
    Statement
    Reference
    Suppressed by
    Statement
    Reference

    sogY506 has denticle phenotype, suppressible by dpphr4/dpp[+]

    sogY506 has denticle phenotype, suppressible by Med[+]/Med15

    sogY506 has denticle phenotype, suppressible by fafFO8/faf[+]

    Other
    Additional Comments
    Genetic Interactions
    Statement
    Reference

    dpphr4/+ partially suppresses the cuticle phenotype of sogY506 hemizygous embryos, partially restoring denticles and producing a curved body.

    Med15/+ partially suppresses the cuticle phenotype of sogY506 hemizygous embryos. The embryos have partially restored denticles, a normal body shape and misplaced, misshapen Filzkorper.

    fafFO8/+ partially suppresses the cuticle phenotype of sogY506 hemizygous embryos. The embryos have partially restored denticles, a normal body shape and poorly developed Filzkorper.

    The mesoderm is able to spread out over the ectoderm after mesoderm invagination in sogY506 brkM68 double mutant embryos. The mesoderm is able to spread out over the ectoderm after mesoderm invagination in Egfrtop-18A sogY506 brkM68 triple mutant embryos.

    The weak dorsalisation phenotype exhibited by cuticles from sogY506 hemizygous embryos is enhanced to full dorsalisation (transformation of all ventral denticle belts into dorsal hairs) by maternal and zygotic heterozygosity for lack15C.

    The ectoderm of brkM68 sogY506/Y double mutant embryos forms only dorsal-type cuticle hairs and completely lacks ventral denticles. The ventral neurogenic region is deleted. The amnioserosa defect seen in sogY506/Y single mutant embryos is not rescued in the double mutant embryos. sogY506/Y Dp(2;2)DTD48/Dp(2;2)DTD48 embryos have a cuticle phenotype resembling that of brk mutants and on average only one row of sna-expressing neuroblasts is left in the ventral neurogenic region. The amnioserosa defect seen in sogY506/Y single mutant embryos is rescued in the double mutant embryos and there is a large increase in the number of amnioserosa cells compared to wild type.

    Suppressor of the tld14/tld1 lethal phenotype. 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
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    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (6)
    References (25)