FB2026_02 , released June 18, 2026
Allele: Hsap\GBA1RecNciI.UAS
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General Information
Symbol
Hsap\GBA1RecNciI.UAS
Species
H. sapiens
Name
FlyBase ID
FBal0288655
Feature type
allele
Associated gene
Hsap\GBA1
Associated Insertion(s)
Carried in Construct
P{UAS-hGBA.RecNciI}
Key Links
Transgenic product class
missense_variant
(Suzuki et al., 2013)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Suzuki et al., 2013)
Mutagen
in vitro construct
(Suzuki et al., 2013)
Progenitor genotype
Carried in construct
P{UAS-hGBA.RecNciI}
Cytology
Description

UASt regulatory sequences drive expression of Hsap\GBA containing the amino acid replacements L444P, A456P and V460V (this variant is associated with acute neurological abnormalities in human Gaucher disease patients).

(Suzuki et al., 2013)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Hsap\GBA1
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 ( 1 )
      Disease
      Evidence
      References
      model of  Gaucher's disease
      CEA
      (Suzuki et al., 2013)
      Modifiers Based on Experimental Evidence ( 0 )
      Disease
      Interaction
      References
      Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
       
      Disease-implicated variant(s)
       
      This allele represents a human variant implicated in disease.
      (Suzuki et al., 2013)
      GBA1:p.Leu483Pro GBA1:p.Ala495Pro GBA1:p.Val499=
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      GBA:p.Leu444Pro GBA:p.Ala456Pro GBA:p.Val460=
      GBA:p.Leu483Pro GBA:p.Ala495Pro GBA:p.Val499=
      GBA1:p.Leu444Pro GBA1:p.Ala456Pro GBA1:p.Val460=
      Associated human disease model(s)
      External database links
      ClinVar: GBA_4297
      Comments concerning this variant

      GBA double/triple variant associated with acute disease.

      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference

      Expression of Hsap\GBARecNciI.Scer\UAS under the control of Scer\GAL4GMR.PU results in an extreme rough eye phenotype.

      (Suzuki et al., 2013)
      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 (4)
      Reported As
      Symbol Synonym
      Hsap\GBA1RecNciI.UAS
      Hsap\GBARecNciI.Scer\UAS
      Hsap\GBARecNciI.UAS
      hGBARecNciI
      (Suzuki et al., 2013)
      Name Synonyms
      Secondary FlyBase IDs
        References (2)