FB2025_01 , released February 20, 2025
Aberration: Dmel\Df(2L)DS6
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General Information
Symbol
Df(2L)DS6
Species
D. melanogaster
Name
FlyBase ID
FBab0001435
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
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

l(2)38Ea << bk1 << l(2)38Eb << HIS-C << bk2 << Low

Genetic mapping information
Comments
Comments on Cytology

Left limit of break 1 from non-inclusion of l(2)38Ea (FBrf0102956) Right limit of break 1 from inclusion of Hr38 (FBrf0102956) Limits of break 2 from polytene analysis (FBrf0039952)

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.
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    Phenotypic Data
    In combination with other aberrations

    The position effect variegation of the w gene seen in In(1)wm4 flies is partially suppressed by one copy of Df(2L)DS6.

    NOT in combination with other aberrations

    Heterozygous flies show a reduced response of the M pacemaker neurons in the brain to Pdf.

    Hemizygous mutants exhibit an acceleration of the S-Phase of mitosis in larval neuroblasts.

    The Df(2L)DS6 chromosome does not act as a dominant suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion).

    Dominantly causes tergite defects in less than 50% of run3 heterozygotes.

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

    Stocks (2)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (4)
    References (34)