FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Hsap\ATXN10Q.UAS.Tag:FLAG
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General Information
Symbol
Hsap\ATXN10Q.UAS.Tag:FLAG
Species
H. sapiens
Name
FlyBase ID
FBal0190886
Feature type
allele
Associated gene
Hsap\ATXN1
Associated Insertion(s)
Carried in Construct
P{UAS-Hsap\ATX1.0Q.FLAG}
Key Links
Transgenic product class
short_tandem_repeat_contraction
(Mizutani et al., 2005)
Mutagen
Nature of the Allele
Transgenic product class
short_tandem_repeat_contraction
(Mizutani et al., 2005)
Mutagen
in vitro construct
(Mizutani et al., 2005)
Progenitor genotype
Carried in construct
P{UAS-Hsap\ATX1.0Q.FLAG}
Cytology
Description

UASt sequences drive expression of Hsap\ATXN1 without any glutamine-repeat tract, tagged with Tag:FLAG.

(Mizutani et al., 2005)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Hsap\ATXN1
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 ( 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

      Expression of Hsap\ATX10Q.Scer\UAS.T:Zzzz\FLAG, under the control of Scer\GAL4GMR.PF, results in an eye phenotype. The defects include loss of bristles and pigmentation, dented ommatidium, and degeneration of photoreceptors. However, the eye's overall structure and the organization of ommatidia are still maintained. Coexpression of Hsap\BoatScer\UAS.T:Zzzz\FLAG and Hsap\ATX10Q.Scer\UAS.T:Zzzz\FLAG, under the control of Scer\GAL4GMR.PF, causes a more severe eye phenotype, in which eye structure is collapsed and photoreceptors are severely degenerated.

      (Mizutani et al., 2005)
      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 (3)
      Reported As
      Symbol Synonym
      Hsap\ATX10Q.Scer\UAS.T:Zzzz\FLAG
      Hsap\ATXN10Q.Scer\UAS.T:Zzzz\FLAG
      Hsap\ATXN10Q.UAS.Tag:FLAG
      Name Synonyms
      Secondary FlyBase IDs
        References (1)