FB2024_03 , released April 23, 2024
Aberration: Dmel\Df(2R)59AD
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General Information
Symbol
Df(2R)59AD
Species
D. melanogaster
Name
FlyBase ID
FBab0022239
Feature type
chromosomal_deletion
Computed Breakpoints include

59A1-59A3;59D1-59D4

Features within 59A1--59D4
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
P{lacW}blwA2-2-27
(Knoblich and Lehner, 1993)
Mutagen
X ray
(Knoblich and Lehner, 1993)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Kidd et al., 1998, Knoblich and Lehner, 1993)
Breakpoints

59A1-59A3;59D1-59D4

(Kidd et al., 1998, Knoblich and Lehner, 1993)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

l(2)59ABc << bk1 << l(2)59ABb << twi << bk2

Genetic mapping information
Comments

This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).

(Marygold et al., 2007)
Comments on Cytology

Left limit of break 1 from polytene analysis (FBrf0058164) Right limit of break 1 from inclusion of blw (FBrf0104928) Limits of break 2 from polytene analysis (FBrf0058164)

Sequence Crossreferences
DDBJ / EMBL / GenBank
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
    Phenotypic Data
    In combination with other aberrations

    Inferred to overlap with: Df(2R)X58-5.

    (Moore, 1997)
    NOT in combination with other aberrations

    Flies heterozygous for the deletion do not show a Minute bristle phenotype.

    (Marygold et al., 2007)

    The Df(2R)59AD 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).

    (Mason et al., 2004)

    Heterozygosity for Df(2R)59AD results in 1.5% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.

    (Harris et al., 2003)

    Homozygous embryos older than about stage 12 are not detected, presumably due to lethality before this stage. The anterior mesoderm of homozygous embryos lacks hemocytes.

    (Inamdar, 2003)
    Stocks (1)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    This complementation data was intended to describe Df(2R)59AB but "Df(2R)59AD" was written in error: see Brown, 1999.2.14, pers. comm.

    (Walsh and Brown, 1998)
    Synonyms and Secondary IDs (5)
    References (34)