FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\easalaP
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General Information
Symbol
Dmel\easalaP
Species
D. melanogaster
Name
FlyBase ID
FBal0125158
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
ala1
Key Links
Nature of the Allele
Progenitor genotype
Associated Insertion(s)
Cytology
Description

The P{GawB} element insertion is at nucleotide 38 of the eas gene.

Allele components
Component
Use(s)
Inserted element
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

Ten-day old easalaP flies (of either sex) do not exhibit signs of retinal degeneration.

easalaP mutants show no bang-sensitive phenotype, either as homozygotes or as transheterozygotes with eas2 or Df(1)4b18. easalaP mutants have a range of defects in the mushroom body; 36% lack β' and β lobes in both hemispheres, 4.5% lack α' and α vertical lobes in both hemispheres, while 10.5% possess all five lobes in both hemispheres. The remaining flies have different combinations of mushroom body phenotype in the left and right hemisphere. The neuroblasts of eas2 mutants show reduced mitosis in mushroom bodies at the pupal stage. This defect leads to a smaller calyx size than in wild-type flies at the adult stage.

Homozygous flies show fusion of both β and β' lobes with intermediate frequency and a reduction or absence of the α lobes in the central brain. easalaP/Df(1)4b18 adults show a very high frequency of β lobe fusion in the central brain. α lobes are absent. Heterozygotes have no adult central brain defect.

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 (1)
Notes on Origin
Discoverer
Comments
Comments

Excision of the P{GawB} element can revert the mutant phenotype.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (6)