FB2026_02 , released June 18, 2026
Allele: Hsap\MAPTE14.Δ306VQIVYK311.UAS.2N4R.mCherry
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General Information
Symbol
Hsap\MAPTE14.Δ306VQIVYK311.UAS.2N4R.mCherry
Species
H. sapiens
Name
FlyBase ID
FBal0411578
Feature type
allele
Associated gene
Hsap\MAPT
Associated Insertion(s)
Carried in Construct
P{UAS-hMAPT.2N4R.E14.Δ306VQIVYK311.mCherry}
Key Links
Transgenic product class
inframe_deletion
(Ramirez-Moreno et al., 2026)
missense_variant
(Ramirez-Moreno et al., 2026)
Mutagen
Nature of the Allele
Transgenic product class
inframe_deletion
(Ramirez-Moreno et al., 2026)
missense_variant
(Ramirez-Moreno et al., 2026)
Mutagen
in vitro construct
(Ramirez-Moreno et al., 2026)
Progenitor genotype
Carried in construct
P{UAS-hMAPT.2N4R.E14.Δ306VQIVYK311.mCherry}
Cytology
Description

10xUAS regulatory sequences drive expression of the 2N4R isoform of Hsap\MAPT with deletion of the [306]VQIVYK[311] aggregation motif and carrying 14 mutations to glutamates (Thr111, Thr153, Thr175, Thr181, Ser199, Ser202, Thr205, Thr212, Thr217, Thr231, Ser235, Ser396, Ser404 and Ser422); tagged with mCherry.

(Ramirez-Moreno et al., 2026)
Allele components
Component
Use(s)
Regulatory region(s)
UAS
Encoded product / tool
Hsap\MAPT
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 ( 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)
       
      This allele represents a human variant implicated in disease.
      (Ramirez-Moreno et al., 2026)
      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\MAPTE14.Δ306VQIVYK311.UAS.2N4R.mCherry
      Name Synonyms
      Secondary FlyBase IDs
        References (1)