FB2024_03 , released June 25, 2024
Allele: Dmel\ftQ805X
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General Information
Symbol
Dmel\ftQ805X
Species
D. melanogaster
Name
FlyBase ID
FBal0357235
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

A number of mutations have been found at the ft locus relative to the sequenced strain, including a premature stop codon at position 805.

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

C4215428T

Amino acid change:

Q805term | ft-PA

Reported amino acid change:

Q805term

Comment:

19 missense variants were identified in the ft locus in strain in addition to this nonsense mutation. Site of nucleotide substitution in mutant inferred by FlyBase curator 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

ftQ805X clones generated in the larval eye disc lead to frequent ommatidial rotation phenotypes - planar cell polarity defects.

In eyes bearing ft8 clones, the clones are larger than control tissue, suggesting they have some competitive advantage; clonal regions in the eye disc show induction of apoptosis.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

numb15, ftQ805X double mutant clones generated in the larval eye disc lead to frequent ommatidial rotation phenotypes - planar cell polarity defects - both in the larva and in adults.

The few ftQ805X/ft8, numb15/+ adult escapers show medial cross-vein defect (Fig. 6B) and PCP defects in the eye.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer

ftQ805X has been identified as a second-site mutation on the numb15 chromosome.

Separable from: numb15.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
ftQ805X
Name Synonyms
Secondary FlyBase IDs
    References (1)