FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Mef265
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General Information
Symbol
Dmel\Mef265
Species
D. melanogaster
Name
FlyBase ID
FBal0044934
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
D-mef265
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Mutation results in a protein that lacks the carboxy-terminal 25 amino acids.

Amino acid replacement: Q491term.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Nucleotide change:

C9916820T

Amino acid change:

Q493term | Mef2-PA; Q486term | Mef2-PB; Q492term | Mef2-PC; Q517term | Mef2-PD; Q478term | Mef2-PF; Q488term | Mef2-PG; Q486term | Mef2-PH; Q453term | Mef2-PI; Q511term | Mef2-PJ; Q459term | Mef2-PK; Q499term | Mef2-PL

Reported amino acid change:

Q491term

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change

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 ( 0 )
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)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

Mef265/Mef2113 embryos exhibit a reduction in the number of dorsal longitudinal indirect flight muscles to three pairs due to defects in the template splitting process.

Mef225-42/Mef265 trans-heterozygotes exhibit major defects in their indirect flight muscles, based on reduced numbers and abnormal patterning of the dorsal longitudinal indirect flight muscles.

Mef226-6/Mef265 trans-heterozygotes exhibit major defects in their indirect flight muscles, based on reduced numbers and abnormal patterning of the dorsal longitudinal indirect flight muscles.

Mef225-34/Mef265 trans-heterozygotes exhibit a wild-type pattern and number of dorsal longitudinal indirect flight muscles.

Mef265/Mef2424 adults survive at 20-30% rate of sibling classes. Eggs laid by Mef265/+ show 92.3% wild type dorsal appendages, 6.2% reduced dorsal appendages and 1.5% broad dorsal appendages and normal egg length. Eggs laid by Mef265/Mef2424 females show 36.9% wild type dorsal appendages, 24.2% reduced dorsal appendages, 19.9% broad dorsal appendages and short egg length, 8.5% broad dorsal appendages and normal egg length, 6.9% abnormal dorsal appendages with short egg length and 3-6% cup-like eggs with no dorsal appendages and cup-like shape.

The three persistant larval oblique muscles per hemithorax of Mef265/Mef2113 animals escape from histolysis as in wild-type animals. Splitting of these muscles generally does not occur in Mef265/Mef2113 animals in contrast to wild-type, so that the number of dorsal longitudinal indirect flight muscles is reduced.

In homozygous mutant embryos, minor pattern deletions in the somatic muscles are evident. Specification of myoblasts is apparently normal. A low percentage of Mef2113/Mef265 progeny survive to adulthood. These survivors are flightless and their dorsal longitudinal muscles are reduced.

External Data
Interactions
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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 (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (4)