FB2024_03 , released June 25, 2024
Allele: Dmel\robo2lea-1
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General Information
Symbol
Dmel\robo2lea-1
Species
D. melanogaster
Name
FlyBase ID
FBal0011612
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Nature of the Allele
Allele class
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

Homozygous embryos show a low frequency of muscles crossing the ventral midline. 36% of inner Fas2-positive axons cross the ventral midline at stages 16 and 17.

Embryos have a mutant central nervous system phenotype. lea1/leaS4-14 embryos have a defective head skeleton and the H-piece does not form. The dorsal bridge still forms.

Head involution is incomplete. Abdominal transformations occur in combination with Pc-like mutants.

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

The number of ventral muscles that cross the midline in lea1 Sdcunspecified double mutant embryos is significantly increased compared to either single mutant. The longitudinal axons collapse along the ventral midline and form a single fascicle. Sdcunspecified homozygous embryos that are also heterozygous for lea1 show an enhanced axonal guidance defect with multiple midline crossings of the fascicles.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (4)