FB2024_03 , released June 25, 2024
Aberration: Dmel\Df(2R)WMG
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General Information
Symbol
Df(2R)WMG
Species
D. melanogaster
Name
FlyBase ID
FBab0002046
Feature type
chromosomal_deletion
Computed Breakpoints include

52A9-52A10;52D9-52D15

Features within 52A9--52D15
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Awasaki and Kimura, 1997, Duffy et al., 1996, Harbecke and Lengyel, 1995, Pauli et al., 1995, Hellmich et al., 1994, Rabinow et al., 1991, Bopp et al., 1989, Schupbach and Wieschaus, 1989, Davis and MacIntyre, 1988, Chase and Kankel, 1987)
Breakpoints

52A4-52B12;52D9-52D15

(Chase and Kankel, 1987)

52A4-52B2;52D7-52E1

(Davis and MacIntyre, 1988)

52C4;52E3

(Awasaki and Kimura, 1997, Bopp et al., 1989)

52A;52D

(Duffy et al., 1996, Harbecke and Lengyel, 1995, Pauli et al., 1995, Schupbach and Wieschaus, 1989)

52A9-52A10;52D12-52D15

(Rabinow et al., 1991)

52A2-52B4;52D7-52E1

(Hellmich et al., 1994)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

bk1 << l(2)52ACh << l(2)52Db << bk2 << Got1

Genetic mapping information
Comments
Comments on Cytology

Limits of break 1 from polytene analysis (FBrf0054158) Limits of break 2 from polytene analysis (FBrf0046776)

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
    NOT in combination with other aberrations

    The Df(2R)WMG 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)

    Mutant embryos show complete fusion of the longitudinal and commissural nerve trunks - few intersegmental connections are maintained.

    (Battye et al., 2001)

    Acts as a dosage sensitive maternal modifier of run : causes tergite defects in greater than 50% of run3 heterozygotes.

    (Duffy et al., 1996)

    Homozygous embryos show defects in segmentation, germband retraction, dorsal closure and head involution. Elongation of Malpighian tubule material is variable.

    (Harbecke and Lengyel, 1995)

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

    (Pauli et al., 1995)
    Stocks (2)
    Notes on Origin
    Discoverer

    Gelbart.

     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (4)
    Reported As
    Symbol Synonym
    Df(2R)WMG
    (Tan et al., 2020, Carmon et al., 2010, Babu and Ramachandra, 2007, Usui-Aoki et al., 2005, Keene et al., 2004, Davis and MacIntyre, 1988)
    Df(2R)WMG268-18
    Df(2R)WMG268.12
    (MacIntyre, 2007.8.30, Chase and Kankel, 1987)
    Df(2R)WMG268-18
    (Davis and MacIntyre, 1988)
    Name Synonyms
    Secondary FlyBase IDs
    • FBab0002047
    References (32)