FB2025_01 , released February 20, 2025
Allele: Hsap\MAPTR406W.UAS.1N4R
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General Information
Symbol
Hsap\MAPTR406W.UAS.1N4R
Species
H. sapiens
Name
FlyBase ID
FBal0284418
Feature type
allele
Associated gene
Hsap\MAPT
Associated Insertion(s)
Carried in Construct
P{UAS-tau.1N4R.R406W}
Key Links
Transgenic product class
missense_variant
(Folwell et al., 2010)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Folwell et al., 2010)
Mutagen
in vitro construct
(Folwell et al., 2010)
Progenitor genotype
Carried in construct
P{UAS-tau.1N4R.R406W}
Cytology
Description

UAS regulatory sequences drive expression of a R406W mutant of the 1N4R Hsap\MAPT-isoform.

(Folwell et al., 2010)
Allele components
Component
Use(s)
Regulatory region(s)
UAS
Encoded product / tool
Hsap\MAPT
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  tauopathy
      CEA
      (Folwell et al., 2010)
      model of  Alzheimer's disease
      CEA with Hsap\APPAβ42.UAS.cUa
      (Folwell et al., 2010)
      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
      Phenotype Manifest In
      Additional Comments
      Genetic Interactions
      Statement
      Reference
      Xenogenetic Interactions
      Statement
      Reference

      Co-expression of Hsap\APPAβ42.Scer\UAS.cUa with Hsap\MAPTR406W.Scer\UAS.1N4R under the control of Scer\GAL4Toll-6-D42 exacerbates the neuromuscular junction (NMJ) aberrations seen in mutants expressing Hsap\APPAβ42.Scer\UAS.cUa alone resulting in a very extreme form of the phenotype.

      (Folwell et al., 2010)
      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
      Hsap\MAPTR406W.Scer\UAS.1N4R
      Hsap\MAPTR406W.UAS.1N4R
      Name Synonyms
      Secondary FlyBase IDs
        References (1)