FB2024_03 , released June 25, 2024
Allele: Dmel\konC452
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General Information
Symbol
Dmel\konC452
Species
D. melanogaster
Name
FlyBase ID
FBal0217365
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: W198term.

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

G18495404A

Amino acid change:

W198term | kon-PB; W198term | kon-PC; W198term | kon-PD

Reported amino acid change:

W198term

Comment:

G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation

(exact site of mutation unspecified). Site of nucleotide substitution in mutant inferred by FlyBase base

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

The four ventral-longitudinal muscles (VL1-4) generally have a rounded morphology and fail to connect to any tendon cell in the abdominal segments of konC41/konC452 embryos.

Muscle VL1 exhibits a rounded morphology in approximately 80% of cases in konC452, konC452/konC25, konC452/konC1139 and konC452/Df(2L)TW137 embryos. In most of the remaining cases, the VL1 muscle fails to span the entire abdominal segment.

The VL1 muscle founder cell is seen at its normal posterior location in konC452/konC1139 embryos at the appropriate stage. VL1 also polarises normally and the anterior end begins its directed migration in the mutant embryos. However, during this anterior migration, defects are seen; the VL1 muscle appears to terminate prematurely compared to wild type and although filopodial extensions of the VL1 muscle do often reach the anterior segment border, they apparently fail to recognise their attachment sites, as no connection is established. The unattached myotubes continue to project filopodia in all directions, but no longer sustain a directed migration towards their target.

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
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (3)