FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Hakai1
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General Information
Symbol
Dmel\Hakai1
Species
D. melanogaster
Name
FlyBase ID
FBal0247657
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Cytology
Description

A deletion allele of Hakai isolated by P-element excision of P{SUPor-P}HakaiKG01389. Lacks the coding region covering the N-terminus and the RING finger 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

Most homozygotes complete embryogenesis and become motile larvae, but die at some point during the larval stage - no viable adults are recovered.

Hakai1 homozygotes partially rescued by Scer\GAL4da.G32-mediated expression of HakaiScer\UAS.T:Ivir\HA exhibit minor morphological abnormalities including small wings, kinked legs and short life span. Some of the rescued flies are sterile.

Hakai1 wing disc clones proliferate at a rate comparable to their wild type twin clones. Adult flies carrying Hakai1 clones develop wings of normal size and shape - the only noticeable defect is occasional duplications of mechanosensory bristles.

Hakai1 germline clones complete normal oogenesis but most fertilized embryos die before hatching. Cuticle defects range from poorly formed denticles, to discontinuity/loss of denticle belts, to a near absence of exoskeleton. Head involution and dorsal closure are also defective. Segmentation is disrupted and epithelial integrity is lost. In rare cases, paternally rescued escapers develop to adulthood.

Endoderm and visceral mesoderm fail to reach the proper positions in embryos lacking maternal and zygotic Hakai, leading to defective midgut formation.

Migrating tracheal cells of Hakai1 germline clone-derived embryos have misshapen and misrouted dorsal branch termini - some cells are only loosely associated with the rest of the branch. Duplication of terminal cells is frequent. Abnormally long filopodia are found extending in the wrong direction.

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
Partially rescued by
Comments

Expression of HakaiScer\UAS.T:Ivir\HA using Scer\GAL4da.G32 partially rescues Hakai1 lethality - 41% of the expected progeny are now viable.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (2)