FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Hsap\L1CAMRSLE-.UAS
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General Information
Symbol
Hsap\L1CAMRSLE-.UAS
Species
H. sapiens
Name
FlyBase ID
FBal0241455
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

UASt regulatory sequences drive expression of the non-neuronal RSLE- isoform of Hsap\L1CAM.

Allele components
Component
Use(s)
Encoded product / tool
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

Expression of Hsap\L1CAMRSLE-.Scer\UAS under the control of Scer\GAL4MS1075 results in a low but not significant level of bristle mechanosensory (BM) axonal defects.

Expression of Hsap\L1CAMRSLE-.Scer\UAS under the control of Scer\GAL4MS1075 induces few phenotypic alterations. No ectopic expression alterations are found in the ocellar sensory system and only a weak gain of function phenotype is observed in the wing.

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

Expression of Hsap\L1CAMRSLE-.Scer\UAS under the control of Scer\GAL4OK307 significantly suppresses the giant fibre axon guidance defects seen in Nrg849 mutant flies.

Expression of Hsap\L1CAMRSLE-.Scer\UAS under the control of Scer\GAL4OK307 suppresses the Giant Fibre (GF)-Trochanteral Muscle (TTM) synaptic defects seen in flies expressing Nrg180ΔFIGQY in a Nrgl4 mutant background; there is an increase in following frequencies after a train of stimulations at 100Hz and response latency is decreased. All flies observed show TTM responses upon GF stimulation. The morphology of the synaptic terminals is restored.

Expression of Hsap\L1CAMRSLE-.Scer\UAS under the control of Scer\GAL4MS1075 suppresses the bristle mechanosensory (BM) axonal defects seen in Nrgl3 mutant flies.

Expression of Hsap\L1CAMRSLE-.Scer\UAS under the control of Scer\GAL4MS1075 in Nrgl3 mutant individuals rescues the axonal defects in OP axons, along with slightly reducing the level of BM axon defects.

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
Hsap\L1CAMRSLE-.Scer\UAS
Hsap\L1CAMRSLE-.UAS
Name Synonyms
Secondary FlyBase IDs
    References (3)