FB2025_01 , released February 20, 2025
Allele: Dmel\AktUAS.ORF
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General Information
Symbol
Dmel\AktUAS.ORF
Species
D. melanogaster
Name
FlyBase ID
FBal0286871
Feature type
allele
Associated gene
Dmel\Akt
Associated Insertion(s)
Carried in Construct
M{UAS-Akt.ORF}
Key Links
Transgenic product class
wild_type
(Schertel et al., 2013)
Mutagen
Nature of the Allele
Transgenic product class
wild_type
(Schertel et al., 2013)
Mutagen
in vitro construct
(Schertel et al., 2013)
Progenitor genotype
Carried in construct
M{UAS-Akt.ORF}
Cytology
Description

UASt regulatory sequences drive expression of a full-length Akt1 open reading frame with its native stop codon.

(Schertel et al., 2013)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Akt
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

      Expression of Akt1UAS.ORF under the control of Scer\GAL4nSyb.PS does not lead to any synaptic overgrowth at neuromuscular junction (assessed by number of boutons and NMJ length) nor any significant changes in crawling velocity in third instar larvae.

      (West et al., 2018)
      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

      The neuromuscular junction synaptic overgrowth and larval locomotion deficits along with the abnormal brain accumulations of POSH protein induced by Scer\GAL4nSyb.PS-driven expression of Hsap\CHMP2BIntron5.UAS is ameliorated by co-expression of Akt1UAS.ORF.

      (West et al., 2018)
      Complementation and Rescue Data
      Comments
      Images (0)
      Mutant
      Wild-type
      Stocks (1)
      Notes on Origin
      Discoverer
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (3)
      Reported As
      Symbol Synonym
      Akt1Scer\UAS.ORF
      Akt1UAS.ORF
      AktUAS.ORF
      Name Synonyms
      Secondary FlyBase IDs
        References (3)