FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\tsrV7M.UAS.Tag:HA
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General Information
Symbol
Dmel\tsrV7M.UAS.Tag:HA
Species
D. melanogaster
Name
FlyBase ID
FBal0362277
Feature type
allele
Associated gene
Dmel\tsr
Associated Insertion(s)
Carried in Construct
P{UAS-tsr.V7M.3HA}
Key Links
Genomic Maps

Transgenic product class
missense_variant
(Balakrishnan et al., 2020)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Balakrishnan et al., 2020)
Mutagen
in vitro construct
(Balakrishnan et al., 2020)
Progenitor genotype
Carried in construct
P{UAS-tsr.V7M.3HA}
Cytology
Description

UAS regulatory sequences drive expression of tsr (from the LD06785 cDNA clone), mutated to carry a V7M amino acid substitution. This mutation is equivalent to the same amino acid change in the orthologous human CFL2 gene, a variant identified in patients with less severe cases of nemaline myopathy. The coding sequence is tagged at the C-terminal end with 3xTag:HA.

(Balakrishnan et al., 2020)
Allele components
Component
Use(s)
Regulatory region(s)
UAS
Encoded product / tool
tsr
Tagged with
Tag:HA
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
point_mutation
2R:24,045,167..24,045,167 [-]
Nucleotide change:

G24045167A

Reported nucleotide change:

G>A

Amino acid change:

V7M | tsr-PA

Reported amino acid change:

V7M

Comment:

Analogous V7M mutation in human CFL2 implicated in nemaline myopathy 7; mutation carried on in vitro construct.

(Balakrishnan et al., 2020)
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  nemaline myopathy 7
      CEA
      (Balakrishnan et al., 2020)
      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.
      (Balakrishnan et al., 2020)
      CFL2:p.Val7Met
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      Associated human disease model(s)
      External database links
      ClinVar: 60554
      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
      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
      tsrV7M.UAS.Tag:HA
      Name Synonyms
      Secondary FlyBase IDs
        References (2)