FB2026_03 , released September 17, 2026
Allele: Dmel\Mi-2H1151R.UAS
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General Information
Symbol
Dmel\Mi-2H1151R.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0344833
Feature type
allele
Associated gene
Dmel\Mi-2
Associated Insertion(s)
Carried in Construct
M{UAS-Mi-2.H1151R}
Key Links
Genomic Maps

Transgenic product class
missense_variant
(Kovač et al., 2018)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Kovač et al., 2018)
Mutagen
in vitro construct
(Kovač et al., 2018)
Progenitor genotype
Carried in construct
M{UAS-Mi-2.H1151R}
Cytology
Description

UASt regulatory sequences drive expression of a mutated form of Mi-2 that carries the H1153R amino acid replacement. This mutation is equivalent to the H1151R mutation in the orthologous human CHD4 gene that has been identified in endometrial carcinoma.

(Kovač et al., 2018)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Mi-2
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
point_mutation
3L:19,885,004..19,885,005 [-]
Nucleotide change:

AC19885005GA

Reported nucleotide change:

CAC>CGA

Amino acid change:

H1153R | Mi-2-PA; H1154R | Mi-2-PB; H1153R | Mi-2-PC; H1144R | Mi-2-PD

Reported amino acid change:

H1153R

Comment:

Analogous H1151R mutation in human CHD4 implicated in cancer, multiple, epigenetic mechanisms; mutation carried on in vitro construct.

(Kovač 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 ( 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.
      (Kovač et al., 2018)
      CHD4:p.His1151Arg
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      CHD4:p.His1138Arg
      CHD4:p.His1144Arg
      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
      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
      Mi-2H1151R.UAS
      Name Synonyms
      Secondary FlyBase IDs
        References (2)