FB2026_02 , released June 18, 2026
Allele: Dmel\pasi1Δ
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General Information
Symbol
Dmel\pasi1Δ
Species
D. melanogaster
Name
FlyBase ID
FBal0316520
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Caused by aberration
Cytology
Description

Imprecise excision of the progenitor, resulting in deletion of the entire pasi1 locus (and 59bp of the 3' UTR of CG7379).

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Comment:

1.6 kb deletion resulting from the imprecise excision of P{EP}G4182 removes sequences spanning 3R:17794826..17796435 .

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

pasi1Δ or pasi1Δ/Df(3R)ED5785 or pasi1Δ/Df(3R)BSC566 embryos have a leaky blood-brain barrier. The number and positions of subperineurial glia are normal. Tracheal tubes of these mutants do not fill with air - the tracheal barrier is also compromised - and dorsal trunks are excessively elongated and convoluted. Septate junctions appear discontinuous and severely disorganized at the blood-brain barrier of pasi1Δ embryos. At embryonic stage 15, septate junction markers are also mislocalized in the hindgut and trachea.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

The leaky blood-brain barrier phenotype of pasi1Δ embryos is not rescued by Scer\GAL4repo-mediated expression of pasi2Scer\UAS.cDa.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Scer\GAL4repo-mediated expression of pasi1Scer\UAS.cDa restores blood-brain barrier function, but not the tracheal defects, in pasi1Δ embryos.

Scer\GAL4repo-mediated expression of pasi1Scer\UAS.T:Avic\GFP restores blood-brain barrier function to pasi1Δ embryos.

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
Name Synonyms
Secondary FlyBase IDs
    References (1)