FB2026_02 , released June 18, 2026
Allele: Hsap\RAF1D486G.UAS
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General Information
Symbol
Hsap\RAF1D486G.UAS
Species
H. sapiens
Name
FlyBase ID
FBal0368730
Feature type
allele
Associated gene
Hsap\RAF1
Associated Insertion(s)
Carried in Construct
P{UAS-hRAF1.D486G}
Key Links
Transgenic product class
missense_variant
(Das et al., 2021)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Das et al., 2021)
Mutagen
in vitro construct
(Das et al., 2021)
Progenitor genotype
Carried in construct
P{UAS-hRAF1.D486G}
Cytology
Description

UASt regulates expression of a Hsap\RAF1 D486G variant found in patients with a RASopathy.

(Das et al., 2021)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Hsap\RAF1
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  Noonan syndrome
      CEA
      (Das et al., 2021)
      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.
      (Das et al., 2021)
      RAF1:p.Asp486Gly
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      RAF1:p.Asp506Gly
      RAF1:p.Asp453Gly
      RAF1:p.Asp405Gly
      RAF1:p.Asp372Gly
      Associated human disease model(s)
      External database links
      ClinVar: 40618
      Comments concerning this variant
      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference

      Expressing Hsap\RAF1D486G.UAS under the control of Scer\GAL4ptc.PU leads to the loss of the L3/L4 crossvein. Expression under the control of Scer\GAL4C-765 results in suppression of venation in the wing.

      (Das et al., 2021)
      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 (1)
      Reported As
      Symbol Synonym
      Hsap\RAF1D486G.UAS
      Name Synonyms
      Secondary FlyBase IDs
        References (2)