FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\robo1ΔIg1.Tag:HA
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General Information
Symbol
Dmel\robo1ΔIg1.Tag:HA
Species
D. melanogaster
Name
FlyBase ID
FBal0320373
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
robo1::robo1ΔIg1
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

2385bp of robo1 upstream flanking sequence drive expression of robo1 amino acid residues 153-1395 (lacks the Ig1 domain). 2192bp of robo1 downstream flanking sequence is also present. The protein is tagged directly upstream of the Ig2 domain with 4 copies of Tag:HA.

Allele components
Component
Use(s)
Regulatory region(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 robo1ΔIg1.T:Ivir\HA1 in the wild-type background has no discernible effect on the structure and morphology of the embryonic ventral nerve cord, not even when two copies of the transgene are present.

Expression of robo1ΔIg1.T:Ivir\HA1 in embryos does not produce any obvious phenotypes in the ventral nerve cord.

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

Co-expression of commScer\UAS.cUa (under the control of Scer\GAL4elav.PLu) and robo1ΔIg1.T:Ivir\HA1 in embryos results in an increase in axon midline crossing and corresponding thickening of commissures in the ventral nerve cord.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of robo1ΔIg1.T:Ivir\HA1 in robo11 mutant background fails to rescue the defects in midline axon repulsion and ectopic midline crossings observed in the ventral nerve cord of robo11 embryos.

Expression of two copies of robo1ΔIg1.T:Ivir\HA1 does not rescue the ventral nerve cord defects, FasII-expressing axon guidance defects or pCC guidance defects of robo11/robo11 mutant embryos.

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
robo1ΔIg1.T:Ivir\HA1
robo1ΔIg1.Tag:HA
Name Synonyms
Secondary FlyBase IDs
    References (3)