FB2025_01 , released February 20, 2025
Allele: Dmel\Mettl5fs
Open Close
General Information
Symbol
Dmel\Mettl5fs
Species
D. melanogaster
Name
FlyBase ID
FBal0362132
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

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

An insertion-deletion (indel) mutation consisting of a deletion of thirteen nucleotides (from base pair 104 to 118) combined with an insertion of three nucleotides, resulting in a frameshift at the amino acid position 36 and a premature stop codon after amino acid 107. If the resulting mRNA would produce only a truncated protein lacking the full methyltransferase domain.

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

Three lesions, two deletions and an insertion, were detected in Mettl5[fs]. The combination of these lesions results in a frameshift after codon 35 (Ile) followed by 73 codons translated out of frame and a premature stop.

Comment:

Three lesions, two deletions and an insertion, were detected in Mettl5[fs]. The combination of these lesions results in a frameshift after codon 35 (Ile) followed by 73 codons translated out of frame and a premature stop.

Inserted_sequence:

CTG

Comment:

Three lesions, two deletions and an insertion, were detected in Mettl5[fs]. The combination of these lesions results in a frameshift after codon 35 (Ile) followed by 73 codons translated out of frame and a premature stop.

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

Mettl5fs/Mettl5fs or Mettl5fs/Df(3L)ED4786 adults are severely disoriented as they changed their walking directions more often than controls.

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
Name Synonyms
Secondary FlyBase IDs
    References (1)