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General Information
Symbol
Dmel\fs(1)NEP1336
Species
D. melanogaster
Name
FlyBase ID
FBal0123270
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
EP(1)1336
Allele class
Nature of the Allele
Allele class
Mutations Mapped to the Genome
 
Type
Location
Additional Notes
References
Associated Sequence Data
DNA sequence
Protein sequence
 
 
Progenitor genotype
Cytology
Nature of the lesion
Statement
Reference

The P{EP} element is inserted 198 nucleotides 5' to the predicted ATG start codon.

Insertion components
P{EP}fs(1)NEP1336
Product class / Tool use(s)
Encoded product / tool
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 )
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In

anterior fascicle & synapse, with Scer\GAL4elav-C155

anterior fascicle & synapse | supernumerary, with Scer\GAL4elav-C155

Detailed Description
Statement
Reference

Mutant larvae expressing fs(1)NEP1336 under the control of Scer\GAL4elav-C155 have strong ISN neuron pathfinding defects. Mutant larvae expressing fs(1)NEP1336 under the control of Scer\GAL4elav-C155 have excessive or ectopic synapses. Mutant larvae expressing fs(1)NEP1336 under the control of Scer\GAL4elav-C155 have reduced or abnormal synapses.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Suppressor of
Phenotype Manifest In
Suppressor of
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer

Selected as: an insertion line that modifies the eye phenotype caused by expression of Ppt1Scer\UAS.cKa under the control of Scer\GAL4GMR.PF when co-expressed using Scer\GAL4GMR.PF.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
fs(1)NEP1336
Name Synonyms
Secondary FlyBase IDs
    References (7)