FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Hsap\TARDBPN267S.UAS.TDPBR
Open Close
General Information
Symbol
Hsap\TARDBPN267S.UAS.TDPBR
Species
H. sapiens
Name
FlyBase ID
FBal0344588
Feature type
allele
Associated gene
Hsap\TARDBP
Associated Insertion(s)
Carried in Construct
M{UAS-hTARDBP.N267S.TDPBR}
Key Links
Transgenic product class
missense_variant
(Miguel et al., 2018)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Miguel et al., 2018)
Mutagen
in vitro construct
(Miguel et al., 2018)
Progenitor genotype
Carried in construct
M{UAS-hTARDBP.N267S.TDPBR}
Cytology
Description

UASt regulatory sequences drive expression of Hsap\TARDBP that has been mutated to carry the N267S amino acid replacement (mutation associated with frontotemporal lobar degeneration). The TDPBR (TDP-43 binding region) regulatory sequence from the Hsap\TARDBP 3' UTR has been inserted downstream of the coding sequence.

(Miguel et al., 2018)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Hsap\TARDBP
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  amyotrophic lateral sclerosis type 10
      CEA
      (Miguel 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.
      (Miguel et al., 2018)
      TARDBP:p.Asn267Ser
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      Associated human disease model(s)
      External database links
      ClinVar: TARDBP_21482
      Comments concerning this variant
      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference

      Expressing Hsap\TARDBPN267S.UAS.TDPBR under the control of Scer\GAL4GMR.PU does not cause a discernible eye phenotypes.

      (Miguel et al., 2018)
      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 (1)
      Notes on Origin
      Discoverer
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (1)
      Reported As
      Symbol Synonym
      Hsap\TARDBPN267S.UAS.TDPBR
      Name Synonyms
      Secondary FlyBase IDs
        References (2)