FB2025_01 , released February 20, 2025
Allele: Hsap\CDH1R749W.UAS
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General Information
Symbol
Hsap\CDH1R749W.UAS
Species
H. sapiens
Name
FlyBase ID
FBal0371581
Feature type
allele
Associated gene
Hsap\CDH1
Associated Insertion(s)
Carried in Construct
P{UAS-hCDH1.R749W}
Key Links
Transgenic product class
missense_variant
(Figueiredo et al., 2022)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Figueiredo et al., 2022)
Mutagen
in vitro construct
(Figueiredo et al., 2022)
Progenitor genotype
Carried in construct
P{UAS-hCDH1.R749W}
Cytology
Description

UAS regulates expression of Hsap\CDH1 containing the R749W variant reported as causative in patients with hereditary diffuse gastric cancer.

(Figueiredo et al., 2022)
Allele components
Component
Use(s)
Regulatory region(s)
UAS
Encoded product / tool
Hsap\CDH1
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 )
      Modifiers Based on Experimental Evidence ( 1 )
      Disease
      Interaction
      References
      model of  gastric diffuse adenocarcinoma
      is ameliorated by mysJF02819
      (Figueiredo et al., 2022)
      Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
       
      Disease-implicated variant(s)
       
      This allele represents a human variant implicated in disease.
      (Figueiredo et al., 2022)
      CDH1:p.Arg749Trp
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      CDH1:p.Arg688Trp
      CDH1:p.Arg233Trp
      CDH1:p.Arg94Trp
      Associated human disease model(s)
      External database links
      ClinVar: 418841
      Comments concerning this variant
      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference

      The expression of Hsap\CDH1R749W.UAS under the control of Scer\GAL4slbo.2.6 leads to a "rough eye" phenotype frequently accompanied by necrosis and pigment loss.

      (Figueiredo 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
      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\CDH1R749W.UAS
      Name Synonyms
      Secondary FlyBase IDs
        References (2)