FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\SmnE33
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General Information
Symbol
Dmel\SmnE33
Species
D. melanogaster
Name
FlyBase ID
FBal0243719
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Cytology
Description

Imprecise excision of the progenitor insertion.

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 ( 1 )
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

SmnE33 mutant larvae exhibit a decrease in locomotion but are more responsive to tail stimuli (i.e. touching of the tail), with a greater number of tail flips, specifically. There is no difference in response to head or abdomen stimuli, compared to controls.

SmnE33 mutant flies are flightless.

SmnX7/SmnE33 third instar larvae have significantly increased evoked excitatory postsynaptic potential amplitude at the neuromuscular junction.

100% of homozygous adults are incapable of flying or jumping.

The mutant indirect flight muscles (IFMs) are highly disorganised; the mutant dorsal longitudinal muscles (DLMs) often fail to extend the whole length of the thorax in contrast to wild type and dorsoventral muscles (DVMs) are typically unidentifiable. The mutant muscles show clear signs of degeneration and are extremely irregular with numerous bulges and constrictions throughout. The mutant myofibers do not show the characteristic striations normally seen in wild-type myofibers. Thick filament formation is largely unperturbed in the mutant indirect flight muscle fibers, while thin filament formation is disrupted.

The number and routing of primary branches of the DLM motoneurons are severely compromised in mutant adults. Secondary branches are disorganised, with arborisation defects ranging from moderate to severe.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Suppressed by
Statement
Reference

SmnE33 has abnormal touch response phenotype, suppressible by w118

NOT suppressed by
Statement
Reference

SmnE33 has abnormal locomotor behavior phenotype, non-suppressible by w118

Other
Statement
Reference
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

The mechanosensory phenotype seen in SmnE33 larvae is rescued by crossing with w118, but crawling speed is not restored to wild-type or SmnE33/+

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

The flightlessness of SmnE33 adults is rescued by expression of SmnScer\UAS.T:Avic\GFP-YFP.Venus under the control of Scer\GAL4da.G32.

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 (5)