Version: 8.1.0
Date: Fri Apr 18 2025
Hsap\WDFY3R2637W.Cterm.UAS.EGFP
FB:FBal0319771Drosophila melanogaster
SummaryTransgenic ConstructsGenomic Variant InformationVariant Molecular ConsequencesPhenotypesDisease Associations
Allele/Variant

Hsap\WDFY3R2637W.Cterm.UAS.EGFP

Species
Drosophila melanogaster
Symbol
Hsap\WDFY3R2637W.Cterm.UAS.EGFP
Category
allele
Allele of gene
None
Transgenic Constructs
Synonyms
  • Hsap\WDFY3[R2637W.Cterm.Scer\UAS.T:Avic\GFP-EGFP]
  • Hsap\WDFY3[R2637W.Cterm.UAS.EGFP]
Description
UASt regulatory sequences drive expression of the C-terminal part of Hsap\WDFY3 (amino acid residues 2285-3526), carrying the amino acid replacement R2637W (this mutation is associated with primary microcephaly in humans). The protein is tagged at the C-terminal end with EGFP.
Additional Information
Literature

Transgenic Constructs

This allele contains 1 transgenic construct
Symbol
P{UAS-WDFY3.R2637W.Cterm.EGFP}
Expressed Components
Knock-down Targets
None
Regulatory Regions
  • UASt
All alleles with this construct

Genomic Variant Information

No data available

Variant Molecular Consequences

No data available

Phenotypes

Phenotype Term
Annotation details
Source
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    Disease Associations

    Association
    Disease Qualifier
    Disease
    Annotation details
    Evidence
    Source
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