FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Vhln1.UAS
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General Information
Symbol
Dmel\Vhln1.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0283408
Feature type
allele
Associated gene
Dmel\Vhl
Associated Insertion(s)
Carried in Construct
P{UAS-Vhl.n1}
Key Links
Genomic Maps

Transgenic product class
frameshift_truncation
(Micale et al., 2009)
Mutagen
Nature of the Allele
Transgenic product class
frameshift_truncation
(Micale et al., 2009)
Mutagen
in vitro construct
(Micale et al., 2009)
Progenitor genotype
Carried in construct
P{UAS-Vhl.n1}
Cytology
Description

UASt regulates expression of a nonsense mutant of Vhl - a c.172delG frameshift mutation located in exon 1 of Vhl, corresponding to the c.163delG pathogenic mutation in human VHL.

(Micale et al., 2009)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Vhl
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
deletion
2R:11,280,049..11,280,049 [+]
Comment:

Analogous c.163delG mutation in human VHL implicated in von Hippel-Lindau syndrome; mutation carried on in vitro construct. Deletion of a single nucleotide results in a frameshift and a premature stop shortly thereafter.

(Micale et al., 2009)
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)
       
      This allele represents a human variant implicated in disease.
      (Micale et al., 2009)
      VHL:p.Glu55fs
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      Associated human disease model(s)
      External database links
      ClinVar: VHL_428800
      Comments concerning this variant
      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference
      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 (3)
      Reported As
      Symbol Synonym
      VhlScer\UAS.n1
      Vhln1.Scer\UAS
      Vhln1.UAS
      Name Synonyms
      Secondary FlyBase IDs
        References (3)