FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Ablftz.PH
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General Information
Symbol
Dmel\Ablftz.PH
Species
D. melanogaster
Name
FlyBase ID
FBal0285358
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Progenitor genotype
Carried in construct
Cytology
Description

The neurogenic enhancer element of ftz drives expression of a wild-type Abl cDNA.

Allele components
Component
Use(s)
Regulatory region(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

Co-expression of Ablftz.PH and AblKN.Scer\UAS suppresses all abnormal axonal crossovers.

Co-expression of two copies of each AblKN.ftz and Ablftz.PH in Abl4 homozygous mutants results in axonal midline crossovers in 54% of embryos, a value almost identical to that observed in Abl4 mutants alone.

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 rescues
Comments

When two copies of Ablftz.PH are introduced into Abl4 mutants, axonal crossovers are reduced from 53% in Abl4 single mutants to 39% in the presence of the transgene.

When two copies of Ablftz.PH are introduced into Abl2 mutants, axonal crossovers are reduced from 68% in Abl2 single mutants to 37% in the presence of the transgene.

Co-expression of two copies of each AblKN.ftz and Ablftz.PH in Abl4 homozygous mutants results in axonal midline crossovers in 54% of embryos, a value almost identical to that observed in Abl4 mutants alone.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
Ablftz.PH
Name Synonyms
Secondary FlyBase IDs
    References (1)