FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\pbl09645
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General Information
Symbol
Dmel\pbl09645
Species
D. melanogaster
Name
FlyBase ID
FBal0009614
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
l(3)09645
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description

P{PZ} insertion 492bp upstream of the AUG start codon of the 1A cDNA.

Allele components
Component
Use(s)
Inserted element
Encoded product / tool
Mutations Mapped to the Genome
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

98% of hemisegments show ISNb guidance defects in homozygous embryos. The ISNb axons often fail to defasciculate from one another, resulting in an abnormally thick morphology and a failure to reach their muscle targets. In addition, ISNb axons that follow aberrant pathways and fasciculate ectopically with adjacent axons (including the transverse nerve) are seen.

90% of hemisegments show defects in the SNa axon in homozygous embryos. The dorsal or lateral SNa branches are often missing.

ISN axons fail to target the correct muscles in homozygous embryos. The first or second branches often extend dorsally beyond their correct muscle fields. Occasionally mutant ISN axons cross the segment boundary and fasciculate with adjacent ISN axons.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
NOT Enhancer of
Statement
Reference
NOT Suppressor of
Statement
Reference
Phenotype Manifest In
NOT Enhancer of
Statement
Reference

pbl[+]/pbl09645 is a non-enhancer of eye phenotype of Hsap\MECP2Δ166.UAS, Scer\GAL4GMR.PU

Suppressor of
Statement
Reference

pbl[+]/pbl09645 is a suppressor of eye phenotype of Hsap\MECP2UAS.FL, Scer\GAL4GMR.PU

NOT Suppressor of
Statement
Reference

pbl[+]/pbl09645 is a non-suppressor of eye phenotype of Hsap\MECP2Δ166.UAS, Scer\GAL4GMR.PU

Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Partially rescued by
Comments

Expression of pblScer\UAS.N.T:Ivir\HA1 under the control of Scer\GAL4how-24B fails to rescue the motor axon pathfinding defects seen in pbl09645 embryos.

Expression of pblScer\UAS.N.T:Ivir\HA1 under the control of Scer\GAL4sca-537.4 partially but significantly rescues the pathfinding defects in the ISNb and SNa, but not the ISN, motor axon pathways in pbl09645 embryos.

Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer

A. Spradling.

Comments
Comments

Excision of the P{lacW} is accompanied by a reversion to wild-type.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (9)