FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\par-1R792G.UAS.Tag:HA
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General Information
Symbol
Dmel\par-1R792G.UAS.Tag:HA
Species
D. melanogaster
Name
FlyBase ID
FBal0359005
Feature type
allele
Associated gene
Dmel\par-1
Associated Insertion(s)
Carried in Construct
PBac{UAS-par-1.R792G.HA}
Key Links
Genomic Maps

Transgenic product class
missense_variant
(Ansar et al., 2018)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Ansar et al., 2018)
Mutagen
in vitro construct
(Ansar et al., 2018)
Progenitor genotype
Carried in construct
PBac{UAS-par-1.R792G.HA}
Cytology
Description

UAS regulates expression of par-1 based on full-length cDNA RE47050 tagged with Tag:HA, and bearing a R792G equivalent to R570G in human MARK3, which is associated with congenital vision loss and progressive eye degeneration.

(Ansar et al., 2018)
Allele components
Component
Use(s)
Regulatory region(s)
UAS
Encoded product / tool
par-1
Tagged with
Tag:HA
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
point_mutation
2R:19,478,750..19,478,750 [+]
Nucleotide change:

A19478750G

Reported nucleotide change:

A>G

Amino acid change:

R792G | par-1-PA; R952G | par-1-PH; R792G | par-1-PL; R1005G | par-1-PR; R786G | par-1-PS; R1017G | par-1-PT; R791G | par-1-PW; R792G | par-1-PX

Reported amino acid change:

R792G

Comment:

Analogous R570G mutation in human MARK3 implicated in visual impairment and progressive phthisis bulbi; mutation carried on in vitro construct.

(Ansar et al., 2018)
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  visual impairment and progressive phthisis bulbi
      CEA
      (Ansar et al., 2018)
      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.
      (Ansar et al., 2018)
      MARK3:p.Arg570Gly
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      MARK3:p.Arg491Gly
      MARK3:p.Arg554Gly
      Associated human disease model(s)
      External database links
      ClinVar: 599409
      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
      par-1R792G.UAS.Tag:HA
      Name Synonyms
      Secondary FlyBase IDs
        References (2)