FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Tmem43S333L.UAS.Tag:HA
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General Information
Symbol
Dmel\Tmem43S333L.UAS.Tag:HA
Species
D. melanogaster
Name
FlyBase ID
FBal0376127
Feature type
allele
Associated gene
Dmel\Tmem43
Associated Insertion(s)
Carried in Construct
P{UAS-Tmem43.S333L.HA}
Key Links
Genomic Maps

Transgenic product class
missense_variant
(Klinke et al., 2022)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Klinke et al., 2022)
Mutagen
in vitro construct
(Klinke et al., 2022)
Progenitor genotype
Carried in construct
P{UAS-Tmem43.S333L.HA}
Cytology
Description

UASt regulates expression of Tag:HA-tagged Tmem43 with a p.S333L substitution, homologous to p.S358L in human TMEM43, which is associated with a rare form of arrhythmogenic right ventricular cardiomyopathy.

(Klinke et al., 2022)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Tmem43
Tagged with
Tag:HA
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
point_mutation
3L:7,913,919..7,913,919 [-]
Nucleotide change:

C7913919T

Amino acid change:

S333L | Tmem43-PA

Reported amino acid change:

S333L

Comment:

Analogous mutation in human TMEM43 implicated in arrhythmogenic right ventricular cardiomyopathy; mutation carried on in vitro construct; site of nucleotide substitution in fly gene inferred by FlyBase curator based on reported amino acid change.

(Klinke et al., 2022)
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  arrhythmogenic right ventricular dysplasia 5
      CEA
      (Klinke et al., 2022)
      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.
      (Klinke et al., 2022)
      TMEM43:p.Ser358Leu
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      Associated human disease model(s)
      External database links
      ClinVar: 734
      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 (1)
      Reported As
      Symbol Synonym
      Tmem43S333L.UAS.Tag:HA
      Name Synonyms
      Secondary FlyBase IDs
        References (2)