FB2026_02 , released June 18, 2026
Aberration: Dmel\Df(2L)C
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General Information
Symbol
Df(2L)C
Species
D. melanogaster
Name
FlyBase ID
FBab0001428
Feature type
Computed Breakpoints include
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Class of aberration (relative to wild type)
Class of aberration (relative to progenitor)
Breakpoints

h35-h37;h35-h37

Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

l(2)40Fa << bk1 << l(2)40Fc << l(2)40Fg << bk2 << l(2)41Ab

Genetic mapping information
Comments
Comments on Cytology

Deficiency of basal heterochromatin.

Left limit of break 1 from polytene analysis (FBrf0080317) Right limit of break 1 from inclusion of cta (FBrf0054123) Left limit of break 2 from inclusion of l(2)40Fd (FBrf0028786) Right limit of break 2 from polytene analysis (FBrf0080317)

Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Genes NOT Deleted / Disrupted
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
    NOT in combination with other aberrations

    Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.

    Stocks (0)
    Notes on Origin
    Discoverer
     

    reconstitution of chromosome 2 by detachment of compound second chromosomes.

    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    Group C deficiencies have been generated from the progenitor genotype of C(2L)RM-SH3 in combination with C(2R)RM-SH3

    Synonyms and Secondary IDs (3)
    Reported As
    Symbol Synonym
    Df(2L)C
    Df(2L)PR31
    Name Synonyms
    Secondary FlyBase IDs
      References (11)