FB2025_01 , released February 20, 2025
Aberration: Dmel\Df(3R)ME15
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General Information
Symbol
Df(3R)ME15
Species
D. melanogaster
Name
FlyBase ID
FBab0022402
Feature type
chromosomal_deletion
Computed Breakpoints include

81F3-81F6;82F5-82F7

Features within 81F3--82F7
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
(Carpenter, 1999, Carpenter, 1994)
Breakpoints

81F3-81F6;82F5-82F7

(Carpenter, 1999, Carpenter, 1994)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

bk1 << l(3)82Fb << l(3)82Fc << bk2 << l(3)82Fj

Genetic mapping information
Comments
Comments on Cytology

All limits from polytene analysis (FBrf0075380)

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 (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 Df(3R)ME15 results in 0.6% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.

    (Harris et al., 2003)

    Shows dominant enhancement of dominant haltere phenotype caused by Ubx195 and Ubx9.22.

    (Burnette et al., 1999)
    Stocks (1)
    Notes on Origin
    Discoverer

    A.T.C. Carpenter.

    (Carpenter, 1994)
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    The Df(3R)ME15 chromosome may 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), but the eye colour phenotype in the presence of Df(3R)ME15 overlaps the eye colour phenotype in a wild-type background so it cannot be unequivocally demonstrated that the deficiency chromosome uncovers a suppressor of telomeric silencing.

    (Mason et al., 2004)

    kkv has been found to fail to complement Df(3R)3-4 and to complement Df(3R)ME15, placing it in 82F5-82F11, contradicting earlier work that placed kkv between 83C1 and 84B2 (FBrf0041709).

    (Ostrowski et al., 2002)
    Synonyms and Secondary IDs (3)
    Reported As
    Symbol Synonym
    DF(3R)ME15
    (Harris et al., 2003)
    Df(3R)ME15
    (Fernandes and Rao, 2011, McElwain et al., 2011, Sinsimer et al., 2011, Tang et al., 2006)
    Df81F3-82F5,7
    (Green and Piergentili, 2000)
    Name Synonyms
    Secondary FlyBase IDs
      References (24)