FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\LamCR264W.UAS
Open Close
General Information
Symbol
Dmel\LamCR264W.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0370597
Feature type
allele
Associated gene
Dmel\LamC
Associated Insertion(s)
Carried in Construct
P{UAS-LamC.R264W}
Key Links
Genomic Maps

Transgenic product class
missense_variant
(Hinz et al., 2021)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Hinz et al., 2021)
Mutagen
in vitro construct
(Hinz et al., 2021)
Progenitor genotype
Carried in construct
P{UAS-LamC.R264W}
Cytology
Description

UASt regulatory sequences drive expression of a full-length LamC cDNA, mutated to carry a R264W amino acid substitution. This change is equivalent to a R249W change in the orthologous human LMNA gene, a variant identified in a patient with muscular dystrophy.

(Hinz et al., 2021)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
LamC
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
MNV
2R:14,572,457..14,572,459 [-]
Nucleotide change:

CGT14572459TGG

Amino acid change:

R264W | LamC-PA; R264W | LamC-PB

Reported amino acid change:

R264W

Comment:

Analogous R249W mutation in human LMNA implicated in muscular dystrophy, congenital, LMNA-related; mutation carried on in vitro construct; site of nucleotide substitution in fly gene inferred by FlyBase curator based on reported amino acid change.

(Hinz et al., 2021)
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  congenital muscular dystrophy due to LMNA mutation
      CEA
      (Hinz et al., 2021)
      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.
      (Hinz et al., 2021)
      LMNA:p.Arg249Trp
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      LMNA:p.Arg137Trp
      LMNA:p.Arg168Trp
      Associated human disease model(s)
      External database links
      ClinVar: 14524
      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
      LamCR264W.UAS
      Name Synonyms
      Secondary FlyBase IDs
        References (2)