FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\HtrA2G363S.UAS
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General Information
Symbol
Dmel\HtrA2G363S.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0288464
Feature type
allele
Associated gene
Dmel\HtrA2
Associated Insertion(s)
Carried in Construct
P{UAS-HtrA2.G363S}
Key Links
Genomic Maps

Transgenic product class
missense_variant
(Yun et al., 2008)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Yun et al., 2008)
Mutagen
in vitro construct
(Yun et al., 2008)
Progenitor genotype
HtrA2UAS.cYa
(Yun et al., 2008)
Carried in construct
P{UAS-HtrA2.G363S}
Cytology
Description

UASt regulatory sequences drive expression of a mutant form of HtrA2 in which the glycine at amino acid 363 has been replaced by serine.

(Yun et al., 2008)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
HtrA2
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
point_mutation
3R:14,510,250..14,510,252 [-]
Comment:

Analogous mutation in human HTRA2 implicated in Parkinson disease 13 mutation carried on in vitro construct; site of nucleotide substitution in fly gene inferred by FlyBase curator based on reported amino acid change.

(Yun et al., 2008)
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.
      (Yun et al., 2008)
      HTRA2:p.Gly399Ser
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      Associated human disease model(s)
      External database links
      ClinVar: HTRA2_4341
      Comments concerning this variant
      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference

      Expression of HtrA2G363S.Scer\UAS under the control of Scer\GAL4GMR.PF at 25[o]C results in a small, rough eye phenotype.

      Indirect flight muscle integrity is disrupted when HtrA2G363S.Scer\UAS is expressed under the control of Scer\GAL4Mef2.PR.

      (Yun et al., 2008)
      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 (2)
      Reported As
      Symbol Synonym
      HtrA2G363S.Scer\UAS
      HtrA2G363S.UAS
      Name Synonyms
      Secondary FlyBase IDs
        References (2)