FB2024_03 , released June 25, 2024
Allele: Dmel\Sosx122
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General Information
Symbol
Dmel\Sosx122
Species
D. melanogaster
Name
FlyBase ID
FBal0030260
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

    Sosx122 homozygous clones in the dorsal air sac primordium grow more slowly than wild-type clones and never contribute to the tip of the primordium.

    Additional cells enter the second mitotic wave in Sosx122 clones.

    Sosx122/SosAM14 flies show loss of wing veins.

    Clonal analysis reveals phenotypes in the adult including loss of wing vein, ectopic wing vein, reduced cell size, extra bristles and cell lethality.

    Defects in the developing central and peripheral nervous system, partial disruption of axon tracts in the commissures and in the longitudinal connectives and disorganisation of sense organ neurons. Heteroallelic combination Sosx122/Sos34Ea-7 displays an extreme rough eye phenotype, many R cells are missing and combination Sosx122/Sosex63 displays a weak rough eye phenotype, R7 cells are missing.

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Suppressed by
    Statement
    Reference

    Sosx122 has visible | recessive phenotype, suppressible by Src42ASu(Raf)1-1

    Suppressor of
    Statement
    Reference

    Sosx122/Sos[+] is a suppressor of visible phenotype of Scer\GAL4en-e16E, Socs44AUAS.cRa

    Other
    Phenotype Manifest In
    Suppressed by
    Statement
    Reference

    Sosx122 has eye phenotype, suppressible by Src42ASu(Raf)1-1

    Sosx122 has wing vein phenotype, suppressible by Src42A7-4

    Suppressor of
    Statement
    Reference

    Sosx122/Sos[+] is a suppressor of phenotype of Src42ASu(Raf)1-1

    Sosx122 is a suppressor of phenotype of Src42AKR.hs.2sev

    NOT Suppressor of
    Statement
    Reference

    Sosx122 is a non-suppressor of photoreceptor cell R7 phenotype of B-H1sev.PH

    Other
    Additional Comments
    Genetic Interactions
    Statement
    Reference

    No second mitotic wave is observed in Su(H)del47, Sosx122 clones.

    The ectopic wing vein phenotype caused by expression of Socs44AScer\UAS.cRa under the control of Scer\GAL4en-e16E is suppressed by Sosx122/+.

    Src42ASu(phl)1-1 dominantly suppresses the rough eye phenotype of Sosx122/SosAM14. The Sosx122/SosAM14 wing vein phenotype is partially suppressed by one copy of Src42A7-4.

    Dominantly suppresses the ability of Src42ASu(phl)1-1 to suppress the lethality of phl1/Y flies.

    Sosx122 significantly suppresses the formation of extra outer photoreceptors caused by B-H1sev.PH, although it does not affect the loss of R7 cell phenotype caused by B-H1sev.PH.

    Although Sos+/Sosx122 shows no phenotype, S54, Sos+/S+,Sosx122 shows a significantly increased numbers of ommatidia with incomplete sets of R cells.

    Sosx122 gene product is capable of suppressing the sev6 phenotype but the level of suppression is lower than that provided by the wild type Sos protein.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Rescued by
    Comments

    The Sosx122 lethal phenotype is rescued by Sos+t15.1.

    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (4)
    References (16)