FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\spn-E4E2-14
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General Information
Symbol
Dmel\spn-E4E2-14
Species
D. melanogaster
Name
FlyBase ID
FBal0151417
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Amino acid replacement: R695term.

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

C15841580T

Amino acid change:

R696term | spn-E-PA

Reported amino acid change:

R695term

Comment:

The mutaiton was reported as R695@. There is no R at position 695 in the reference sequence. The closest R residues are at 694 and 696. The mutation was mapped to R696. It isn't possible to create a stop with a single nucleotide change for R694 (CGT). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.

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

The eggs laid by spn-E4E2-14/spn-Ehls-Δ125 mutant females exhibit severe dorsoventral patterning defects, with a high percentage of collapsed eggs or eggs with no dorsal appendages.

spn-Ehls-Δ157/spn-E4E2-14 oocytes have thick microtubule bundles and rapid cytoplasmic movement.

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 (0)
Notes on Origin
Discoverer

Selected as: a mutant that results in defective localisation of an Avic\GFP-stau marker in living oocytes in females containing homozygous germ-line clones.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
spn-E4E2-14
Name Synonyms
Secondary FlyBase IDs
    References (2)