FB2026_02 , released June 18, 2026
Gene: Dsim\Nmy
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Important message

Updated sequence information for this Drosophila species is no longer provided by FlyBase. Gene model annotations for this species are now updated and maintained at NCBI, using the gnomon automated annotation pipeline. See the NCBI page ‘Eukaryotic genomes annotated at NCBI’.

The FlyBase BLAST tool will continue to support queries against the reference genome of this species, but not queries against annotated transcripts or proteins. For the current release, there is no JBrowse or GBrowse view of the gene model annotations for this species.

The FlyBase archived release FB2017_05 includes the last NCBI annotation update for this species that was imported into FlyBase. That sequence data can be accessed from archived gene reports, via the archived GBrowse tool, and via archived bulk-data downloads.

General Information
Symbol
Dsim\Nmy
Species
D. simulans
Name
Not much yang
Annotation Symbol
Feature Type
FlyBase ID
FBgn0260751
Gene Model Status
Stock Availability
Gene Summary
Contribute a Gene Snapshot for this gene.
Also Known As

Nmy

Summaries
Alleles, Insertions, Transgenic Constructs, and Aberrations
Classical and Insertion Alleles ( 4 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 0 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of Dsim\Nmy
Transgenic constructs containing regulatory region of Dsim\Nmy
Aberrations (Deficiencies and Duplications) ( 0 )
Inferred from experimentation ( 0 )
Variants
Variant Molecular Consequences
Alleles Representing Disease-Implicated Variants
Phenotypes
For more details about a specific phenotype click on the relevant allele symbol.
Phenotype manifest in
Allele
Orthologs
Model Organism Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Drosophila melanogaster (Fruit fly) (0)
Human Disease Associations
FlyBase Human Disease Model Reports
    Disease Ontology (DO) Annotations
    Models Based on Experimental Evidence ( 0 )
    Allele
    Disease
    Evidence
    References
    Potential Models Based on Orthology ( 0 )
    Human Ortholog
    Disease
    Evidence
    References
    Modifiers Based on Experimental Evidence ( 0 )
    Allele
    Disease
    Interaction
    References
    Disease Associations of Human Orthologs (via DIOPT v9.1 and OMIM)
    Note that ortholog calls supported by only 1 or 2 algorithms (DIOPT score < 3) are not shown.
    Homo sapiens (Human)
    Gene name
    Score
    OMIM
    OMIM Phenotype
    DO term
    Complementation?
    Transgene?
    Functional Complementation Data
    Functional complementation data is computed by FlyBase using a combination of the orthology data obtained from DIOPT and OrthoDB and the allele-level genetic interaction data curated from the literature.
    Interactions
    Summary of Physical Interactions
    Interaction Browsers
    Summary of Genetic Interactions
    Interaction Browsers
    Starting gene(s)
    Interaction type
    Interacting gene(s)
    Reference
    Starting gene(s)
    Interaction type
    Interacting gene(s)
    Reference
    External Data
    Linkouts
    Class of Gene
    Stocks and Reagents
    Stocks (0)
    Genomic Clones (0)
     
      cDNA Clones (0)
       

      Please Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see JBrowse for alignment of the cDNAs and ESTs to the gene model.

      cDNA clones, fully sequenced
      BDGP DGC clones
        Other clones
          Drosophila Genomics Resource Center cDNA clones

          For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.

            cDNA Clones, End Sequenced (ESTs)
            BDGP DGC clones
              Other clones
                RNAi and Array Information
                Linkouts
                Antibody Information
                Laboratory Generated Antibodies
                 
                Commercially Available Antibodies
                 
                Cell Line Information
                Publicly Available Cell Lines
                 
                  Other Stable Cell Lines
                   
                    Other Comments

                    Annotation GD10714 eliminated in release 2.01 of the Drosophila simulans genome annotation; not predicted by NCBI Gnomon predictions dated 2014.10.09).

                    Dsim\Nmy appears to have limited coding potential.

                    The Dsim\Dox gene is an X-linked sex-ratio meiotic drive distorter. It functions solely as a sex-ratio distorter and is not an essential gene (mutant males have normal sex ratio and spermatogenesis). The Dsim\Dox gene was the precursor for the origin of its autosomal suppressor Dsim\Nmy by a retrotransposition process. Dsim\Nmy is dispensible if Dsim\Dox function is absent. The structures of the Dsim\Dox and Dsim\Nmy genes suggests that an RNAi mechanism may be involved in the suppression of Dsim\Dox by Dsim\Nmy, as the Dsim\Nmy transcript appears to be able to form a stem-loop structure with a dsRNA stem of 345bp.

                    Relationship to Other Genes
                    Source for database merge of

                    Source for merge of: Dsim\nmy Dsim\GD10714

                    Additional comments

                    FlyBase Curator comment: Identity between 'Dsim\nmy' and 'Dsim\GD10714' determined from analysis of GenBank sequence EF565211 and primer sequences in Figure 1D.

                    Dsim\Nmy appears to have arisen by insertion of sequence into the region of the D.simulans genome that is homologous to the CG14370 gene from D.melanogaster (evidence suggests that this occurred in a common ancestor before the split between D.simulans and D.mauritiana). Sequence comparisons strongly suggest that Dsim\Nmy originated from part of Dsim\Dox through retrotransposition. First, there is a tandem duplication of the dinucleotide TA at the insertion site within the sequences homologous to CG14370 and 11bp (TTGTTTAATTT) that are proximal to the 5' end of the Dsim\Dox cDNA are also duplicated in the 5' end of the Dsim\Nmy insert. Second, the three introns of Dsim\Dox are not found in Dsim\Nmy. On the other hand, the 3' end of Dsim\Nmy matches to the genomic region 100-200bp upstream of Dsim\Dox, and so it is unclear whether the precursor mRNA in the retrotransposition event was a bona fide transcript of Dsim\Dox. Other than the leftmost inverted repeat, sequences of Dsim\Nmy and Dsim\Dox are largely colinear, implying that this inverted repeat originated as a secondary duplication after the retrotransposition.

                    Nomenclature History
                    Source for database identify of

                    Source for identity of: Dsim\Nmy Dsim\nmy

                    Nomenclature comments
                    Etymology
                    Synonyms and Secondary IDs (10)
                    Reported As
                    Name Synonyms
                    Not Much Yang
                    Not much yang
                    Secondary FlyBase IDs
                    • FBgn0069482
                    • FBgn0182478
                    Datasets (0)
                    Study focus (0)
                    Experimental Role
                    Project
                    Project Type
                    Title
                    Study result (0)
                    Result
                    Result Type
                    Title
                    External Crossreferences and Linkouts ( 0 )
                    References (14)