FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\FoxK44
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General Information
Symbol
Dmel\FoxK44
Species
D. melanogaster
Name
FlyBase ID
FBal0298977
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

fd68A44 mutants carry a deletion of 2bp at the insertion site of P{EP}fd68AEP3428 and contains a reinsertion of a fragment of the p-element in exon 3 that generates a premature STOP codon 28 nucleotides after the insertion, resulting in a truncated protein that retains the FHA domain but lacks the FH domain.

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

Early midgut differentiation is normal in fd68A44 mutant embryos until stage 15, when the midgut is composed of a single vesicle. During stage 16 three constrictions generate the four vesicles of the normal midgut. However, fd68A44 homozygous embryos form a single midgut constriction and two gastric vesicles. The midgut does not develop further.

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

Double heterozygous dpps12; fd68A44 mutants exhibit almost 100% lethality.

Double heterozygous dpps8; fd68A44 mutants exhibit almost 100% viability.

Double heterozygous dpphr27; fd68A44 mutants exhibit almost 80% viability.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (1)