FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\wgNE2
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General Information
Symbol
Dmel\wgNE2
Species
D. melanogaster
Name
FlyBase ID
FBal0094277
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: C242Y. Nucleotide substitution: G to A.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Nucleotide change:

G7314373A

Reported nucleotide change:

G?A

Amino acid change:

C242Y | wg-PA

Reported amino acid change:

C242Y

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

wgNE2 mutants exhibit a reduction in the zone of naked cuticle on the ventral side in between the denticle belts as well as a disruption of dorsal patterning, leading to a strong curvature of the embryonic cuticle.

Mutant embryos exhibit a strong loss of cluster II slou expressing muscle founder cells and a weak loss of cluster I slou expressing muscle founder cells.

Homozygous embryos secrete patches of naked cuticle and denticle belts containing predominantly row 5 type denticles, with a low frequency of other denticle morphologies. Segmental pattern in the dorsal cuticle is abolished and the dorsal expanse is greatly reduced.

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

The wgNE2 mutant ventral patterning phenotype is suppressed by SoxNNC14 to almost wild-type levels without rescuing dorsal patterning.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Fails to complement
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (3)