FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\sqhT20A
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General Information
Symbol
Dmel\sqhT20A
Species
D. melanogaster
Name
FlyBase ID
FBal0374376
Feature type
allele
Associated gene
Dmel\sqh
Associated Insertion(s)
Carried in Construct
P{sqh.T20A}
Key Links
Transgenic product class
missense_variant
(Doerflinger et al., 2022)
polypeptide_post_translational_processing_variant
(Doerflinger et al., 2022)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Doerflinger et al., 2022)
polypeptide_post_translational_processing_variant
(Doerflinger et al., 2022)
Mutagen
in vitro construct
(Doerflinger et al., 2022)
Progenitor genotype
Carried in construct
P{sqh.T20A}
Cytology
Description

2.7kb genomic fragment that encompasses sqh. The coding sequence has been mutated to carry a T20A amino acid substitution (mutation of the second phosphorylation site to a non-phosphorylatable residue).

(Doerflinger et al., 2022)
Allele components
Component
Use(s)
Regulatory region(s)
sqh
Encoded product / tool
sqh
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Variant Molecular Consequences
Associated Sequence Data
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
 
UniProtKB/Swiss-Prot
    UniProtKB/TrEMBL
      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

      sqhAX3 heterozygotes bearing two copies of sqhT20A produce oocytes with polarity defects (i.e. mislocalized Staufen protein).

      (Doerflinger et al., 2022)
      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
      Fails to rescue

      sqhT20A fails to rescue sqhAX3

      (Doerflinger et al., 2022)
      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
      sqhT20A
      Name Synonyms
      Secondary FlyBase IDs
        References (1)