FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Diap1UAS.Tag:HA
Open Close
General Information
Symbol
Dmel\Diap1UAS.Tag:HA
Species
D. melanogaster
Name
FlyBase ID
FBal0123674
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
P[UAS-diap1]
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

UASt sequences drive expression of Diap1 tagged with the first four residues of MNPV(Op)\Iap3 followed by a 9 amino acid Tag:HA tag which is fused in frame to sequences immediately following the second methionine of the original Diap1 sequence.

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
External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Suppressor of
Statement
Reference
NOT Suppressor of
Statement
Reference
Phenotype Manifest In
Suppressor of
Statement
Reference
NOT Suppressor of
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

The border follicle cell migration defect seen in egg chambers expressing Rac1N17.Scer\UAS under the control of Scer\GAL4slbo.2.6 is partially suppressed by coexpression of thScer\UAS.T:Ivir\HA1. The border follicle cell migration defect seen in egg chambers expressing PvrDN.Scer\UAS under the control of Scer\GAL4slbo.2.6 is suppressed by coexpression of thScer\UAS.T:Ivir\HA1 (the frequency of migration defects is less than 10% in the rescued egg chambers). The penetrance of the embryonic lethal phenotype caused by expression of Rac1N17.Scer\UAS under the control of Scer\GAL469B or Scer\GAL4pnr-MD237 is reduced by coexpression of thScer\UAS.T:Ivir\HA1. The embryonic cuticle phenotype (dorsal hole) caused by expression of Rac1N17.Scer\UAS under the control of Scer\GAL469B or Scer\GAL4pnr-MD237 is rescued by coexpression of thScer\UAS.T:Ivir\HA1. The dramatic defects in myoblast fusion caused by expression of Rac1N17.Scer\UAS under the control of Scer\GAL4how-24B are not rescued by coexpression of thScer\UAS.T:Ivir\HA1.

Co-expression of WScer\UAS.cZa and rprScer\UAS.cZa (when driven by Scer\GAL4Gp150-52A) results in ectopic midline cell death. The addition of thScer\UAS.T:Ivir\HA1 suppresses this phenotype, sometimes to wild-type.

Xenogenetic Interactions
Statement
Reference
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 (3)
Reported As
Symbol Synonym
Diap1Scer\UAS.T:Ivir\HA1
Diap1UAS.Tag:HA
thScer\UAS.T:Ivir\HA1
Name Synonyms
Secondary FlyBase IDs
    References (6)