FB2026_02 , released June 18, 2026
Allele: Dmel\stl2
Open Close
General Information
Symbol
Dmel\stl2
Species
D. melanogaster
Name
FlyBase ID
FBal0016195
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
stlAWK26
Key Links
Genomic Maps

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

Amino acid replacement (Q to stop) at a position that corresponds to residue 101 in the B isoform, and residue 146 in the C isoform (not applicable to the A isoform). Also, an amino acid replacement (T to I) at a position that corresponds to residue 99 in the A isoform (not applicable to the B and C isoforms).

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

C22812338T

Amino acid change:

Q146term | stl-PC; Q146term | stl-PE

Reported amino acid change:

Q146term

Reported_genomic_loc:

2R_r5:18699843..18699843

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. One of two amino acid changes observed in mutant. Amino acid change only applies to two isoforms since the short form starts downstream of the nonsense mutation.

Nucleotide change:

C22813408T

Amino acid change:

T445I | stl-PC; T445I | stl-PE

Reported amino acid change:

T99I

Reported_genomic_loc:

2R_r5:18700913..18700913

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. One of two amino acid changes observed in mutant. Only applies to the shortest isoform since translation is terminated before this residue in other isoforms due to the earlier nonsense mutation.

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

stl2 and stl2/stl4 mutant embryos display significantly faster dorsal migration of the v'ch1 sensory neuron during stages 15-17, to its target the lch5 chordotonal organ cluster, as compared to wild type, and no over-migration past its target.

Mutant ovarioles in adult females lack the interfollicular stalks that normally separate adjacent wild-type follicles. This phenotype results from failed follicle individualisation, rather than from persistent germline cell division, because mutant ovarioles contain germ cells at varying stages of maturation and groups of 16 interconnected germ cells that would correspond to a single germline cyst in wild-type are still recognisable. Degeneration is seen in the mutant ovarioles, which increases with age, and both germline and somatic cells appear to degenerate.

stl4/stl2 females lack morphological stalks in the ovary.

Abnormal numbers of nurse cells and tumorous egg chambers.

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 (5)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (5)