FB2025_01 , released February 20, 2025
Aberration: Dmel\Df(3L)HR119
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General Information
Symbol
Df(3L)HR119
Species
D. melanogaster
Name
FlyBase ID
FBab0002322
Feature type
chromosomal_deletion
Computed Breakpoints include

63C6;63F7

Features within 63C6--63F7
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
P{C28C}
(Wohlwill and Bonner, 1991)
Mutagen
X ray
(Wohlwill and Bonner, 1991)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Mogila, 1998.3.19, Thomas et al., 1998, Zhimulev et al., 1998, Deak et al., 1997, Zhimulev et al., 1997.9.29, Coyne, 1996, Hawkins et al., 1996, Curtiss and Heilig, 1995, Wohlwill and Bonner, 1991)
Breakpoints

63C6;63E

(Mogila, 1998.3.19, Coyne, 1996, Hawkins et al., 1996, Curtiss and Heilig, 1995, Wohlwill and Bonner, 1991)

63C2;63F7

(Zhimulev et al., 1998, Zhimulev et al., 1997.9.29)

63C6;63E9

(Thomas et al., 1998, Deak et al., 1997)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

kst << bk1 << l(3)63Da << Sc2 << bk2 << dib

Genetic mapping information
Comments
Comments on Cytology

Limits of break 1 from polytene analysis (FBrf0054184) Limits of break 2 from polytene analysis (FBrf0098597)

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.
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    Phenotypic Data
    In combination with other aberrations

    Inferred to overlap with: Df(3L)BSC129.

    (Andrade et al., 2005.10.27)

    Viable when heterozygous with Df(3L)HR218.

    (Wohlwill and Bonner, 1991)
    NOT in combination with other aberrations

    The Df(3L)HR119 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(3L)HR119 results in 1.9% X chromosome nondisjunction and 0.3% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.

    (Harris et al., 2003)

    Dominantly suppresses the KrIf-1/+ eye phenotype.

    (Carrera et al., 1998)

    Causes inviability or low viability in hybrid females when heterozygous with D.simulans chromosome.

    (Coyne et al., 1998)

    Weak second site non-complementing phenotype with zipEbr and zipmhc-c6.1 : malformed phenotype penetrance 10-24%.

    (Halsell and Kiehart, 1998)

    Shows no maternal enhancement of dpphr4.

    (Nicholls and Gelbart, 1998)

    Deficient embryos show an uninterpretable mutant midgut phenotype.

    (Bilder and Scott, 1995)
    Stocks (2)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    "63C2;63F7" was stated as revision.

    (Zhimulev et al., 1998, Zhimulev et al., 1997.9.29)

    Used in D.melanogaster/D.simulans hybrids to map at least four non-overlapping regions on the D.simulans 3R that have effects on the species difference of cuticular hydrocarbon profile.

    (Coyne, 1996)
    Synonyms and Secondary IDs (5)
    References (55)