FB2025_01 , released February 20, 2025
Allele: Dmel\shakB22
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General Information
Symbol
Dmel\shakB22
Species
D. melanogaster
Name
FlyBase ID
FBal0015595
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
shakBEC201, EC201, PasEC201
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Amino acid replacement: W273term.

The premature stop codon is in exon G of shakB and is predicted to result in a truncated protein that lacks the C-terminal 100 amino acids of the wild-type protein.

Nucleotide substitution: G1657A.

Mutation in the lethal and neural common exons. Amino acid replacement: W262@. Nucleotide substitution: TGG to TGA. Residue lies in the membrane-spanning domain.

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

G20773259A

Reported nucleotide change:

G1657A

Amino acid change:

W273term | shakB-PA; W262term | shakB-PC; W433term | shakB-PD; W217term | shakB-PE; W193term | shakB-PF; W278term | shakB-PG; W278term | shakB-PH; W278term | shakB-PI

Reported amino acid change:

W273term

Comment:

TGG to TGA

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

Lethal and neural allele. Fails to complement the giant fibre system defects of viable shakB alleles.

The DLMs do not respond to brain shocks and the TTMs respond only occasionally and then with a longer than normal latency.

Abnormal electrophysiological phenotype. Homozygous flies exhibit uncoordinated leg movements under ether anaesthesia and do not jump to a light off stimulus. Heterozygotes are fully viable but exhibit some neuronal defects.

Homozygous germline clones display no maternal effect.

shakB22/shakB2 flies show shaking behaviour.

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

Lefevre.

Comments
Comments

Maternal germline clonal analysis demonstrates there is no maternal effect.

shakB alleles exhibit a complex pattern of complementation.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (6)