FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\droshaR1210W.GR
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General Information
Symbol
Dmel\droshaR1210W.GR
Species
D. melanogaster
Name
FlyBase ID
FBal0385691
Feature type
allele
Associated gene
Dmel\drosha
Associated Insertion(s)
Carried in Construct
PBac{drosha.R1210W.GR}
Key Links
Genomic Maps

Transgenic product class
missense_variant
(Barish et al., 2022)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Barish et al., 2022)
Mutagen
in vitro construct
(Barish et al., 2022)
Progenitor genotype
Carried in construct
PBac{drosha.R1210W.GR}
Cytology
Description

Genomic fragment that encompasses drosha. The coding sequence has been mutated to carry a R1210W amino acid substitution. This change is equivalent to a R1342W change in the orthologous human DROSHA gene, a variant identified in a patient with a severe neurodevelopmental disorder.

(Barish et al., 2022)
Allele components
Component
Use(s)
Regulatory region(s)
drosha
Encoded product / tool
drosha
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
MNV
2R:7,936,201..7,936,203 [+]
Nucleotide change:

CGC7936201TGG

Amino acid change:

R1210W | drosha-PA

Reported amino acid change:

R1210W

Comment:

Analogous R1342W mutation in human DROSHA implicated in neurodevelopmental disorder (postulated), DROSHA-related; mutation carried on in vitro construct; site of nucleotide substitution in fly gene inferred by FlyBase curator based on reported amino acid change.

(Barish et al., 2022)
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.
      (Barish et al., 2022)
      DROSHA:p.Arg1342Trp
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      DROSHA:p.Arg1305Trp
      Associated human disease model(s)
      External database links
      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
      Partially rescues

      droshaR1210W.GR partially rescues droshaW1123X

      (Barish et al., 2022)
      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
      droshaR1210W.GR
      Name Synonyms
      Secondary FlyBase IDs
        References (2)