FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Egfrflb-2E07
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General Information
Symbol
Dmel\Egfrflb-2E07
Species
D. melanogaster
Name
FlyBase ID
FBal0033661
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
flb2E07, egfr2E07, flb2EO7
Key Links
Nature of the Allele
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

Egfrt1/Egfrflb-2E07 animals have rough eyes.

Eggs derived from Egfrt1/Egfrflb-2E07 females are ventralised and have no or only one dorsal appendage.

Homozygous embryos lack all midline glia cells.

Homozygotes display a weak 'flb' phenotype and hemizygotes display an intermediate 'flb' phenotype. Embryos produced from heteroallelic combination with Egfrt1 have a severe ventralised phenotype, reduction in size of their dorsal appendage.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
NOT Enhanced by
Statement
Reference

Egfrflb-2E07 has phenotype, non-enhanceable by rhohs.PSt

Suppressed by
Statement
Reference

Egfrflb-2E07/Egfrt1 has eye phenotype, suppressible | partially by kek1RA5/kek1[+]

Egfrflb-2E07/Egfrt1 has eye phenotype, suppressible | partially by kek1[+]/kek1RM2

NOT suppressed by
Statement
Reference

Egfrflb-2E07 has phenotype, non-suppressible by rhohs.PSt

Additional Comments
Genetic Interactions
Statement
Reference

Heterozygous kek1RM2 or kek1RA5 partially suppresses the rough eye phenotype seen Egfrflb-2E07/Egfrt1 animals. kek1RM2/kek1RA5 fully suppresses the phenotype.

The Egfrt1/Egfrflb-2E07 phenotype is partially suppressed by kek1RA5/kek1RM2.

The ubiquitous expression of rhohs.PSt under heatshock has no effect on Egfrflb-2E07 embryos.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
Comments
Comments

Mutation of Egfr that coordinately affects all gene activities, a class I lesion. The allelic series for class I lesions: Egfrt2 = Egfrt1 < Egfrtop-EC20 < Egfrf7 = Egfrf1 = Egfrflb-2E07 < Egfrtop-EE39 = Egfrtop-ED26 = Egfrf5 < Egfrf9 = Egfrf10 = Egfrf2 = Egfrtop-EE42 = Egfrf11 = Egfrf24 = Egfrf3 = Df(2R)Egfr3.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (8)
Reported As
Name Synonyms
Secondary FlyBase IDs
  • FBal0033664
References (9)