FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\AkhAP
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General Information
Symbol
Dmel\AkhAP
Species
D. melanogaster
Name
FlyBase ID
FBal0319564
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Mutagen
Nature of the Allele
Progenitor genotype
Cytology
Description

19 bp deletion in the region that codes for the AKH octapeptide, producing a frameshift upstream of the coding sequence of the APRP peptide sequence. No translation products from the locus are detected in the mutant flies.

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

A 19bp deletion in Akh leading to a frameshift.

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

AkhAP/AkhAP mutants do not display any abnormalities in hatchability, viability, female fecundity, body size (measured as length of thorax), wing area, adult spontaneous locomotion or climbing, flight performance, carbohydrate and lipid stores between L3 and immature adult stages, corpora cardiaca cell number, or carbohydrate stores in mature adults, as compared to controls.

AkhAP/AkhAP mutants display a small, significant decrease in developmental time. In the first week of adulthood, AkhAP/AkhAP mutants develop obesity (significantly increased glyceride to protein ratio), and significantly decreased circulating sugars in the hemolymph. Adult AkhAP/AkhAP mutants show significantly increased starvation resistance, impaired lipid (but not carbohydrate) mobilization during starvation, suppressed starvation-induced hyperactivity, increased survival in response to paraquat feeding, but also increased paraquat-induced food aversion, and decreased oxidative stress resistance when assayed by paraquat application directly to the nerve cord, as compared to controls.

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
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (6)