FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\fd59A1
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General Information
Symbol
Dmel\fd59A1
Species
D. melanogaster
Name
FlyBase ID
FBal0295499
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Contains a point mutation in the fd59A splice donor site at amino acid 118.

Nucleotide substitution: T?A.

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

T22868856A

Reported nucleotide change:

T?A

Comment:

T to A mutation in splice donor site.

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 fd59A1 mutant flies are viable, morphologically normal, but sub-fertile.

fd59A1/fd59A2 mutant flies are viable, morphologically normal, but are sub-fertile; male mutant flies crossed to control females lay normal number of eggs, but mutant females crossed to control males lay fewer eggs. Even fewer eggs are laid when mutant males are crossed to mutant females.

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

Expression of fd59AScer\UAS.cLa under the control of Scer\GAL4Tdc2.PC rescues the egg laying defect seen in fd59A1/fd59A2 mutant females. The morphology and axonal pathway selection of Tdc2[+] neurons are essentially identical between fd59A1/fd59A2 mutant and wild type controls.

Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
fd59A1
Name Synonyms
Secondary FlyBase IDs
    References (1)