FB2026_02 , released June 18, 2026
Allele: Dmel\fsdKG02393
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General Information
Symbol
Dmel\fsdKG02393
Species
D. melanogaster
Name
FlyBase ID
FBal0157204
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
Associated Insertion(s)
Cytology
Description

P{SUPor-P}fsdKG02393 is inserted 15bp downstream of ATG, disrupting the entire open reading frame.

Allele components
Component
Use(s)
Mutations Mapped to the Genome
Curation Data
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

fsdKG02393 homozygotes are viable, but exhibit a temperature-dependent hatching defect. Although the hatching rates of embryos from wild-type and fsdKG02393 flies are comparable at 25[o]C, embryos from mutant flies exhibit a significantly reduced hatching rate at 18[o]C. At 29[o]C, embryos from fsdKG02393 females exhibit a hatching rate of 0%. These embryos exhibit variable A-P patterning defects including missing/fused denticle bands. This hatching defect at 29[o]C is strictly associated with the maternal mutant genotype and, furthermore, mutant flies at non-optimal temperatures (18[o]C) do not exhibit a significant reduction in survival rates from larvae to pupae or from pupae to adults.

At 25[o]C, fsdKG02393 embryos exhibit a posterior shift of the cephalic furrow position compared to wild-type.

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

The anterior fatemap shift caused by maternal bcd dosage reduction (in bcd6 heterozygotes) is suppressed partially by eliminating fsd maternally (through a fsdKG02393 background).

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
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
CG12765KG02393
Name Synonyms
Secondary FlyBase IDs
    References (3)