FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Hsap\MAPTS352L.UAS.cBa
Open Close
General Information
Symbol
Hsap\MAPTS352L.UAS.cBa
Species
H. sapiens
Name
UAS construct a of Bardai
FlyBase ID
FBal0345177
Feature type
allele
Associated gene
Hsap\MAPT
Associated Insertion(s)
Carried in Construct
P{UAS-hMAPT.S352L}
Key Links
Transgenic product class
missense_variant
(Bardai et al., 2018)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Bardai et al., 2018)
Mutagen
in vitro construct
(Bardai et al., 2018)
Progenitor genotype
Carried in construct
P{UAS-hMAPT.S352L}
Cytology
Description

UAS regulates expression of the "frontotemporal dementia and parkinsonism linked to chromosome 17" (FTDP-17)-linked S352L mutant form of Hsap\MAPT, expressed within the "0N4R" (no N-terminal inserts, four microtubule binding repeat) form of Hsap\MAPT.

(Bardai et al., 2018)
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  frontotemporal dementia
      CEA
      (Bardai et al., 2018)
      model of  tauopathy
      CEA
      (Bardai et al., 2018)
      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.
      (Bardai et al., 2018)
      MAPT:p.Ser669Leu
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      MAPT:p.Ser352Leu
      MAPT:p.Ser744Leu
      MAPT:p.Ser292Leu
      MAPT:p.Ser323Leu
      MAPT:p.Ser687Leu
      Associated human disease model(s)
      External database links
      ClinVar: MAPT_14267
      Comments concerning this variant
      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
      Hsap\MAPTS352L.UAS.cBa
      Name Synonyms
      UAS construct a of Bardai
      Secondary FlyBase IDs
        References (2)