FB2026_02 , released June 18, 2026
Allele: Dmel\lola2B13
Open Close
General Information
Symbol
Dmel\lola2B13
Species
D. melanogaster
Name
FlyBase ID
FBal0039614
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description
Allele components
Component
Use(s)
Inserted element
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

In the embryonic CNS, longitudinal connectives are interrupted and commissures fuse. In some segments the VUM neurons are born and differentiate, but fail to form a well-defined posterior root to the anterior peripheral fascicle. Intersegmental nerve shows various aberrations, failing to grow or wandering into adjacent segments, or defasciculation of ISN sensory axons. The lateral chordotonal organs are sometimes displaced dorsally from their wild type position. There is no segment specificity of these phenotypes.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
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
Comments
Comments

Transposase induced excision of the P element reverts both the lethality and the mutant neuronal phenotype. The ISN phenotype and the lateral chordotonal organ phenotype shows incomplete expressivity. The trachea appear normal in the mutant embryos. The number of PNS neurons, their distribution into neuronal subtypes and differentiation appear normal.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
lola2B13
Name Synonyms
Secondary FlyBase IDs
    References (1)