FB2025_01 , released February 20, 2025
Aberration: Dmel\Df(3R)WIN11
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General Information
Symbol
Df(3R)WIN11
Species
D. melanogaster
Name
FlyBase ID
FBab0002696
Feature type
chromosomal_deletion
Also Known As
Df(3R)Win11
Computed Breakpoints include

83E1-83E2;84B1

Features within 83E1--84A5
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
X ray
(Pattatucci et al., 1991)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Duffy et al., 1996, Pauli et al., 1995, Pattatucci et al., 1991)
Breakpoints

83E1-83E2;84A4-84A5

(Duffy et al., 1996, Pauli et al., 1995, Pattatucci et al., 1991)
Causes alleles
ScrWIN11
(Southworth and Kennison, 2002)
Carries alleles
Transposon Insertions
Formalized genetic data

bk1 << pb << Scr << bk2 << ftz

Genetic mapping information
Comments
Comments on Cytology

Limits of break 1 from polytene analysis (FBrf0054155) Left limit of break 2 from inclusion of Scr (FBrf0054157) Right limit of break 2 from non-inclusion of Antp (FBrf0054157)

Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
gpp
(Shanower et al., 2005)
l(3)PL13
(Slack et al., 2006)
Pak
(Hing et al., 1999)
Scr
(Pattatucci and Kaufman, 1991)
Partially deleted / disrupted
Molecular Data
Completely deleted
Partially deleted
Genes NOT Deleted / Disrupted
Complementation Data
 
Antp
(Pattatucci and Kaufman, 1991)
ftz
(Pattatucci and Kaufman, 1991)
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

    Inferred to overlap with: Df(3R)BSC744.

    (Christensen et al., 2009.2.28)

    Inferred to overlap with: Df(3R)BSC745.

    (Christensen et al., 2009.2.28)

    Inferred to overlap with: Df(3R)BSC746.

    (Christensen et al., 2009.2.28)

    Inferred to overlap with: Df(3R)BSC681.

    (Christensen et al., 2008.12.28)

    Df(3R)WIN11/Df(3R)MAP2 viable Df(3R)WIN11/Df(3R)MAP2 pb-

    NOT in combination with other aberrations

    The Df(3R)WIN11 chromosome acts as a dominant weak 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).

    (Mason et al., 2004)

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

    (Duffy et al., 1996)

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

    (Pauli et al., 1995)
    Stocks (2)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (3)
    References (24)