FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Aberration: Dmel\In(2)bwVde2
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General Information
Symbol
In(2)bwVde2
Species
D. melanogaster
Name
FlyBase ID
FBab0047637
Feature type
chromosomal_inversion
Computed Breakpoints include
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to wild type)
chromosomal_inversion
(Berloco et al., 2014)
Class of aberration (relative to progenitor)
chromosomal_inversion
(Berloco et al., 2014)
Breakpoints
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data
Genetic mapping information
Comments
Comments on Cytology
Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
Partially deleted / disrupted
Molecular Data
Completely deleted
Partially deleted
Genes NOT Deleted / Disrupted
Complementation Data
 
Molecular Data
 
Genes Duplicated
Complementation Data
Completely duplicated
Partially duplicated
Molecular Data
Completely duplicated
Partially duplicated
Genes NOT Duplicated
Complementation Data
 
Molecular Data
 
Affected Genes Inferred by Location (0)
    If no genes are listed here, it may be because the affected region is very large. The JBrowse insert above may show an error for the same reason, and other FlyBase tools such as CytoSearch may also fail for large regions. You can contact FlyBase for more help.
    In these cases, there will be no "Export to Hitlist" button to the left.
    Phenotypic Data
    In combination with other aberrations

    The X heterochromatin in Dp(1)A140 appears to suppress the eye colour variegation phenotype of In(2)bwVde2.

    (Berloco et al., 2014)

    The X heterochromatin in Dp(1;f)1173 appears to suppress the eye colour variegation phenotype of In(2)bwVde2.

    (Berloco et al., 2014)

    The X heterochromatin in Dp(1;f)1187 appears to suppress the eye colour variegation phenotype of In(2)bwVde2.

    (Berloco et al., 2014)

    The X heterochromatin in Dp(1;f)1205 appears to suppress the eye colour variegation phenotype of In(2)bwVde2.

    (Berloco et al., 2014)

    The X heterochromatin in Dp(1;f)1346 appears to suppress the eye colour variegation phenotype of In(2)bwVde2.

    (Berloco et al., 2014)

    The autosomal heterochromatin in Dp(2;f)e51 appears to suppress the eye colour variegation phenotype of In(2)bwVde2.

    (Berloco et al., 2014)

    The autosomal heterochromatin in Dp(2;f)e58 appears to suppress the eye colour variegation phenotype of In(2)bwVde2.

    (Berloco et al., 2014)

    The autosomal heterochromatin in Dp(2;f)e97 appears to suppress the eye colour variegation phenotype of In(2)bwVde2.

    (Berloco et al., 2014)
    NOT in combination with other aberrations
    Stocks (0)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (1)
    Reported As
    Symbol Synonym
    In(2)bwVde2
    (Berloco et al., 2014)
    Name Synonyms
    Secondary FlyBase IDs
      References (1)