FB2026_03 , released September 17, 2026
Allele: Dmel\fs(1)ne3a
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General Information
Symbol
Dmel\fs(1)ne3a
Species
D. melanogaster
Name
FlyBase ID
FBal0004478
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Nature of the Allele
Allele class
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

Homozygous females are sterile, and lay fewer than 1% as many eggs as wild-type. The endochorion has occasional defects, and the respiratory appendages are essentially normal.

Homozygous females lay few or no eggs. Mature follicles of homozygous females have major defects in the endochorion (which are uniformly distributed) but the respiratory appendages are normal.

Oviposition of few if any eggs. Various defects in respiratory appendages and chorionic architecture of hand dissected eggs.

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

double mutant?

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
Comments
Comments

Germ line clonal analysis shows that fs(1)ne3a is germ line-dependent.

Recombination mapping of fs(1)ne3a is not consistent with the phenotype being caused by a single mutation. The phenotype of the fs(1)ne3a chromosome may be caused by two mutations, one at an extreme distal position and one at an extreme proximal position on the chromosome, both of which must be present to confer the "no egg" phenotype. Since two alleles of fs(1)ne3 have been isolated in the same screen, this suggests that at least one mutation was present on the parental chromosome. Germ line clonal analysis shows that fs(1)ne3a is germ line-dependent.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
fs(1)ne31
fs(1)ne3a
Name Synonyms
Secondary FlyBase IDs
    References (2)