FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\mute1281
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General Information
Symbol
Dmel\mute1281
Species
D. melanogaster
Name
FlyBase ID
FBal0246406
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Nucleotide substitution: C559T.

Amino acid replacement: Q187term.

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

C16954532T

Reported nucleotide change:

C559T

Amino acid change:

Q187term | mute-PC

Reported amino acid change:

Q187term

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

Females containing homozygous germline clones do not lay eggs.

Homozygous stage 16 embryos show a severe loss of muscle mass compared to controls.

mute1281/Df(2R)Exel6065 embryos show no significant difference in somatic muscle mass or morphology at stage 14 compared to control embryos. However, by stage 15, some muscles appear thinner than normal in the mutant embryos and some muscles are no longer detectable. At stage 16, many muscles appear significantly thinner than normal in the mutant embryos and some muscles are no longer detectable. This phenotype is not biased to any specific somatic muscle type and some of the muscles appear to detached at least at one end. By stage 17, the muscles have degenerated so that they have lost the characteristic wild-type morphology and are spherical in shape or are extremely thin.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
NOT suppressed by
Statement
Reference
Other
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

The thin muscles characteristic of late stage mute1281/Df(2R)Exel6065 embryos are still seen if they are also homozygous for Df(3L)H99.

More than half of mute1281/+ ; Slbp15/Slbp15 stage 16 embryos have somatic muscles that appear significantly thinner than normal. Some muscles are detached while others appear to be missing.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Partially rescued by
Comments

The muscle wasting phenotype of mute1281/Df(2R)Exel6065 embryos is completely rescued by expression of muteL.Scer\UAS or muteΔC.L.Scer\UAS under the control of Scer\GAL4how-24B.

The muscle wasting phenotype of mute1281/Df(2R)Exel6065 embryos is not rescued by expression of muteΔC-Atro.L.Scer\UAS under the control of Scer\GAL4how-24B.

The muscle wasting phenotype of mute1281/Df(2R)Exel6065 embryos is partially rescued by expression of muteS.Scer\UAS under the control of Scer\GAL4how-24B.

Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (3)