FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\E(bx)ry122
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General Information
Symbol
Dmel\E(bx)ry122
Species
D. melanogaster
Name
FlyBase ID
FBal0031830
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
Nurf3011
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description

The P{ry11} insertion is within the untranslated leader sequence of E(bx).

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

E(bx)ry122 mutants show class I dendrite branching defects at late larval stages.

E(bx)ry122 mutants have a high incidence of melanotic tumours and an increased number of larval hemocytes.

The male X chromosome in E(bx)ry122/Df(3L)3643 mutants is highly aberrant. E(bx)Nurf301-2/E(bx)ry122 and E(bx)ry122/E(bx)Nurf301-3 mutant larvae exhibit melanotic tumours.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
NOT suppressed by
Statement
Reference

E(bx)ry122 has neoplasia phenotype, non-suppressible by Df(2R)ED3921

Enhancer of
Statement
Reference

E(bx)ry122/E(bx)[+] is an enhancer of visible | dominant phenotype of gcmPyx

Phenotype Manifest In
NOT suppressed by
Statement
Reference
Enhancer of
Additional Comments
Genetic Interactions
Statement
Reference

Df(2R)ED3921 fails to suppress the melanotic tumour and increased larval hemocyte number of E(bx)ry122 mutants.

The frequency of abnormal dorsal appendages in embryos derived from females carrying EcRB1-ΔC655.F645A.Scer\UAS under the control of Scer\GAL4slbo.2.6 (23%) is increased if the females are also heterozygous for E(bx)ry122 (84%).

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer

A. Spradling.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (7)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (10)