FB2025_01 , released February 20, 2025
Allele: Dmel\SoxNK439.UAS
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General Information
Symbol
Dmel\SoxNK439.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0197573
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

Amino acid replacement: K439R.

UAS regulatory sequences drive expression of SoxN, that has a K439R substitution which stops the expressed product from being modified with a SUMO group.

Allele components
Component
Use(s)
Encoded product / tool
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

Expression of SoxNK439.Scer\UAS under the control of Scer\GAL4elav.PLu in embryos results in specific defects in the axon scaffolding in the ventral nerve cord, including fusing and widening of the anterior and posterior commissures, thickening of the longitudinal connectives, and tangles at the segmental boundaries.

Expression of SoxNK439.Scer\UAS in the eye disc, driven by Scer\GAL4ey.PB, results in a few adult escapers with a headless phenotype.

Expression of SoxNK439.Scer\UAS in the embryo, under the control of Scer\GAL4da.G32, results in defects in the central nervous system followed by lethality at the end of embryogenesis. CNS defects include the fusion or absence of commissures and the reduction or absence of longitudinal axon tracts.

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
SoxNK439.Scer\UAS
SoxNK439.UAS
Name Synonyms
Secondary FlyBase IDs
    References (2)