FB2024_03 , released June 25, 2024
Allele: Dmel\MhcIFI.S531P.Act88F
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General Information
Symbol
Dmel\MhcIFI.S531P.Act88F
Species
D. melanogaster
Name
FlyBase ID
FBal0369973
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

An Act88F promoter drives expression of the indirect flight muscle myosin isoform (IFI) of Mhc, mutated to carry a S531P amino acid substitution; this mutation is equivalent to a S532P change in the orthologous human MYH7 gene, a pathogenic variant associated with dilated cardiomyopathy. The coding sequence is composed of cDNA sequence encoding the Mhc IFI motor domain followed by a genomic fragment encompassing Mhc exons 12-19 (and associated introns and polyadenylation sites). The protein is tagged at the N-terminal end with Tag:polyHis and with the Tag:CS(TEVp) cleavage site.

Allele components
Component
Use(s)
Regulatory region(s)
Encoded product / tool
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Nucleotide change:

T16776865C

Amino acid change:

S531P | Mhc-PA; S531P | Mhc-PB; S531P | Mhc-PC; S531P | Mhc-PD; S531P | Mhc-PE; S531P | Mhc-PF; S531P | Mhc-PG; S531P | Mhc-PH; S531P | Mhc-PI; S531P | Mhc-PK; S531P | Mhc-PL; S531P | Mhc-PM; S531P | Mhc-PN; S531P | Mhc-PO; S531P | Mhc-PP; S531P | Mhc-PQ; S531P | Mhc-PR; S531P | Mhc-PS; S531P | Mhc-PT; S531P | Mhc-PU; S531P | Mhc-PV

Reported amino acid change:

S531P

Comment:

Mutation in analagous codon in human MYH7 implicated in cardiomyopathy associated with dilated cardiomyopathy 1S; mutation carried on in vitro construct; specific disease association inferred by FlyBase curator based on reported amino acid change; site of nucleotide change determined from primer sequences.

Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
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
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.
MYH7:p.Ser532Pro
Variants Synonym(s)
Associated human disease model(s)
External database links
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
MhcIFI.S531P.Act88F
Name Synonyms
Secondary FlyBase IDs
    References (2)