FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\EphKD
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General Information
Symbol
Dmel\EphKD
Species
D. melanogaster
Name
FlyBase ID
FBal0269902
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Progenitor genotype
Associated Insertion(s)
Cytology
Description

Tandem partial duplication of the Eph locus. One copy is untranslatable and the other bears a 3' deletion encompassing the entire kinase domain. This is predicted to be a partial loss-of-function allele, which still retains reverse-signalling and kinase-independent activities. A w[+] marker and a single FRT site are present between the two copies of Eph.

Allele components
Component
Use(s)
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

Homozygotes display approximately 50% developmental mortality; survivors display normal external adult morphology. Homozygous females exhibit a 60-90% rate of sterility. Olfactory-based learning is significantly impaired. Although adult eye structure and gross retinal development are normal, EphKD third instar larvae display variable defects in the centripetal projections of medulla cortical axons toward the developing neuropil: there are gaps in the crescent-shaped neuropil and ectopic axon bundels in the cell body layer surrounding the neuropil.

All EphKD mutants examined exhibit at least one gap in the medulla neuropil with the majority showing more than one such gap. Half of these animals have normal lobula architecture. Large HRP[+] cortical inclusions are rare.

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

The rough eye phenotype of Scer\GAL4hs.2sev, EphrinScer\UAS.cDa flies is suppressed by EphKD.

All optic lobe phenotypic features associated with EphKD are exacerbated by heterozygosity for Reph1 or Rephk08617A.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
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
Name Synonyms
Secondary FlyBase IDs
    References (2)