FB2026_03 , released September 17, 2026
Allele: Dmel\Prp8S2178F.UAS.Tag:FLAG
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General Information
Symbol
Dmel\Prp8S2178F.UAS.Tag:FLAG
Species
D. melanogaster
Name
FlyBase ID
FBal0361586
Feature type
allele
Associated gene
Dmel\Prp8
Associated Insertion(s)
Carried in Construct
P{UAS-Prp8.S2178F.Flag}
Key Links
Genomic Maps

Transgenic product class
missense_variant
(Stanković et al., 2020)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Stanković et al., 2020)
Mutagen
in vitro construct
(Stanković et al., 2020)
Progenitor genotype
Carried in construct
P{UAS-Prp8.S2178F.Flag}
Cytology
Description

UASt regulatory sequences drive expression of a mutated form of Prp8 that carries a S2178F amino acid substitution. This change is equivalent to a S2118F change in the orthologous human PRPF8 gene, a pathogenic variant associated with retinitis pigmentosa. The coding sequence is tagged at the N-terminal end with Tag:FLAG.

(Stanković et al., 2020)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Prp8
Tagged with
Tag:FLAG
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
point_mutation
2R:12,155,034..12,155,035 [-]
Nucleotide change:

CG12155035TT

Amino acid change:

S2178F | Prp8-PA

Reported amino acid change:

S2178F

Comment:

Analogous S2118F mutation in human PRPF8 implicated in Retinitis pigmentosa 13; mutation carried on in vitro construct.

(Stanković et al., 2020)
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.
      (Stanković et al., 2020)
      PRPF8:p.Ser2118Phe
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      Associated human disease model(s)
      External database links
      ClinVar: 30666
      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 (1)
      Reported As
      Symbol Synonym
      Prp8S2178F.UAS.Tag:FLAG
      Name Synonyms
      Secondary FlyBase IDs
        References (2)