FB2024_02 , released April 23, 2024
Allele: Hsap\HTTQ97.S16D.ex1.UAS.mCherry
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General Information
Symbol
Hsap\HTTQ97.S16D.ex1.UAS.mCherry
Species
H. sapiens
Name
FlyBase ID
FBal0365509
Feature type
allele
Associated gene
Hsap\HTT
Associated Insertion(s)
Carried in Construct
PBac{UAS-hHTT.ex1.Q97.S16D.mCherry}
Key Links
Transgenic product class
inframe_deletion
(Branco-Santos et al., 2017)
missense_variant
(Branco-Santos et al., 2017)
polypeptide_post_translational_processing_variant
(Branco-Santos et al., 2017)
trinucleotide_repeat_expansion
(Branco-Santos et al., 2017)
Mutagen
Nature of the Allele
Transgenic product class
inframe_deletion
(Branco-Santos et al., 2017)
missense_variant
(Branco-Santos et al., 2017)
polypeptide_post_translational_processing_variant
(Branco-Santos et al., 2017)
trinucleotide_repeat_expansion
(Branco-Santos et al., 2017)
Mutagen
in vitro construct - regulatory fusion
(Branco-Santos et al., 2017)
in vitro construct - coding region fusion
(Branco-Santos et al., 2017)
in vitro construct - amino acid replacement
(Branco-Santos et al., 2017)
Progenitor genotype
Carried in construct
PBac{UAS-hHTT.ex1.Q97.S16D.mCherry}
Cytology
Description

UAS regulatory sequences (from the pWalium10-roe vector) drive expression of Hsap\HTT exon 1 with a mutant (expanded) polyQ tail of 97 residues. A phosphomimetic mutation (S16D) has been introduced into the coding sequence, and it is tagged with mCherry.

(Branco-Santos et al., 2017)
Allele components
Component
Use(s)
Regulatory region(s)
UAS
Encoded product / tool
Hsap\HTT
Tagged with
mCherry
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  Huntington's disease
      CEA
      (Branco-Santos et al., 2017)
      Modifiers Based on Experimental Evidence ( 1 )
      Disease
      Interaction
      References
      model of  Huntington's disease
      is ameliorated by Pp1α-96AHMS02477
      (Branco-Santos et al., 2017)
      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
      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\HTTQ97.S16D.ex1.UAS.mCherry
      Name Synonyms
      Secondary FlyBase IDs
        References (1)