FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\p130CASUAS.Tag:MYC
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General Information
Symbol
Dmel\p130CASUAS.Tag:MYC
Species
D. melanogaster
Name
FlyBase ID
FBal0219081
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

UASt regulatory sequences drive expression of p130CAS which is tagged at the N-terminal end with Tag:MYC.

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 ( 1 )
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

Embryos expressing p130CASScer\UAS.T:Hsap\MYC under the control of Scer\GAL4elav.PLu show axon guidance defects in the ISNb pathway, in the SNa pathway and in the central nervous system. The severity of the phenotype is dosage sensitive and the defects seen are characteristic of increased fasciculation in the ISNb pathway.

Embryos expressing p130CASScer\UAS.T:Hsap\MYC under the control of Scer\GAL4p130CAS-NP4466 show axon guidance defects in the ISNb pathway, in the SNa pathway and in the central nervous system. The defects seen are characteristic of increased fasciculation in the ISNb pathway.

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

The axon guidance defects seen in the ISNb pathway, SNa pathway and central nervous system of embryos expressing p130CASScer\UAS.T:Hsap\MYC under the control of Scer\GAL4elav.PLu are significantly rescued by mys1/+.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of p130CASScer\UAS.T:Hsap\MYC under the control of Scer\GAL4p130CAS-NP4466 partially rescues the axon guidance defects seen in the ISNb pathway, SNa pathway and central nervous system of p130CASNP4466/Df(3L)ED201 embryos.

Expression of p130CASScer\UAS.T:Hsap\MYC under the control of Scer\GAL4elav.PLu partially rescues the axon guidance defects seen in the ISNb pathway, SNa pathway and central nervous system of Df(3L)Exel6083 homozygous embryos.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
p130CASScer\UAS.T:Hsap\MYC
p130CASUAS.Tag:MYC
Name Synonyms
Secondary FlyBase IDs
    References (2)