FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Hsap\DHX9R1052Q.UAS.Tag:MYC
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General Information
Symbol
Hsap\DHX9R1052Q.UAS.Tag:MYC
Species
H. sapiens
Name
FlyBase ID
FBal0392589
Feature type
allele
Associated gene
Hsap\DHX9
Associated Insertion(s)
Carried in Construct
P{UAS-hDHX9.R1052Q.MYC}
Key Links
Transgenic product class
missense_variant
(Yamada et al., 2023)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Yamada et al., 2023)
Mutagen
in vitro construct
(Yamada et al., 2023)
Progenitor genotype
Carried in construct
P{UAS-hDHX9.R1052Q.MYC}
Cytology
Description

UASt regulatory sequences drive expression of Hsap\DHX9 carrying the human disease-relevant R1052Q mutation; tagged at the N-terminal with Tag:MYC.

(Yamada et al., 2023)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Hsap\DHX9
Tagged with
Tag:MYC
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 )
      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.
      (Yamada et al., 2023)
      DHX9:p.Arg1052Glu
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      Associated human disease model(s)
        External database links
        Comments concerning this variant

        This variant may or may not be implicated in disease. Related disease model in flies: neurodevelopmental disorder, DHX9-related (FBhh0001537).

        (FlyBase curators, 2019-)
        Phenotypic Data
        Phenotypic Class
        Phenotype Manifest In
        Detailed Description
        Statement
        Reference
        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
        Comments
        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
        DHX9R1052Q
        (Yamada et al., 2023)
        Hsap\DHX9R1052Q.UAS.Tag:MYC
        Name Synonyms
        Secondary FlyBase IDs
          References (2)