FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Hsap\BSNP3866A.UAS
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General Information
Symbol
Hsap\BSNP3866A.UAS
Species
H. sapiens
Name
FlyBase ID
FBal0406395
Feature type
allele
Associated gene
Hsap\BSN
Associated Insertion(s)
Carried in Construct
P{UAS-hBSN.P3866A}
Key Links
Transgenic product class
missense_variant
(Martinez et al., 2022)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Martinez et al., 2022)
Mutagen
in vitro construct
(Martinez et al., 2022)
Progenitor genotype
Carried in construct
P{UAS-hBSN.P3866A}
Cytology
Description

UASt sequences regulate expression of Hsap\BSN carrying a P3866A amino acid substitution. This variant has been identified in patients with pathological aggregation of 3R/4R tau.

(Martinez et al., 2022)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Hsap\BSN
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 ( 1 )
      Disease
      Interaction
      References
      exacerbates  tauopathy
      modeled by Hsap\MAPTP301L.GMR
      (Martinez et al., 2022)
      Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
       
      Disease-implicated variant(s)
       
      This allele represents a human variant implicated in disease.
      (Martinez et al., 2022)
      BSN:p.Pro3866Ala
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      Associated human disease model(s)
        External database links
        Comments concerning this variant

        Exacerbates MAPT-related tauopathy; see Human Disease Model report FBhh0000101.

        (FlyBase curators, 2019-)
        Phenotypic Data
        Phenotypic Class
        Phenotype Manifest In
        Detailed Description
        Statement
        Reference
        External Data
        Interactions
        Show genetic interaction network for Enhancers & Suppressors
        Phenotypic Class
        Enhancer of
        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\BSNP3866A.UAS
        Name Synonyms
        Secondary FlyBase IDs
          References (2)