FB2026_02 , released June 18, 2026
Allele: Hsap\APOL1G1G2.UAS.Tag:FLAG
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General Information
Symbol
Hsap\APOL1G1G2.UAS.Tag:FLAG
Species
H. sapiens
Name
FlyBase ID
FBal0398910
Feature type
allele
Associated gene
Hsap\APOL1
Associated Insertion(s)
Carried in Construct
P{UAS-hAPOL1.G1G2.FLAG}
Key Links
Transgenic product class
inframe_deletion
(Zhu et al., 2023)
missense_variant
(Zhu et al., 2023)
Mutagen
Nature of the Allele
Transgenic product class
inframe_deletion
(Zhu et al., 2023)
missense_variant
(Zhu et al., 2023)
Mutagen
in vitro construct
(Zhu et al., 2023)
Progenitor genotype
Carried in construct
P{UAS-hAPOL1.G1G2.FLAG}
Cytology
Description

UASt sequences regulate expression of a Hsap\APOL1 cDNA that has been mutated to carry both the 'G1' (S342G and I384M amino acid substitutions) and 'G2' (deletion of amino acids N388 and Y389) risk variants for kidney disease. The coding sequence is tagged at the C-terminal end with Tag:FLAG.

(Zhu et al., 2023)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Hsap\APOL1
Tagged with
Tag:FLAG
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Variant Molecular Consequences
Associated Sequence Data
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
 
UniProtKB/Swiss-Prot
    UniProtKB/TrEMBL
      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 ( 1 )
      Disease
      Evidence
      References
      model of  focal segmental glomerulosclerosis
      CEA
      (Zhu et al., 2023)
      Modifiers Based on Experimental Evidence ( 0 )
      Disease
      Interaction
      References
      Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
       
      Disease-implicated variant(s)
       
      This allele represents a human variant implicated in disease.
      (Zhu et al., 2023)

      This combination of multiple mutational lesions affecting a single copy of the gene has not been found in humans.

      (FlyBase curators, 2019-)
      Phenotypic 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
      Comments
      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
      Hsap\APOL1G1G2.UAS.Tag:FLAG
      Name Synonyms
      Secondary FlyBase IDs
        References (2)