FB2025_05 , released December 11, 2025
Aberration: Dmel\Df(3L)rdgC-co2
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General Information
Symbol
Df(3L)rdgC-co2
Species
D. melanogaster
Name
FlyBase ID
FBab0002392
Feature type
chromosomal_deletion
Also Known As
Df(3L)rdgC, Df(3L)rdgCco2
Computed Breakpoints include

77A1;77D1

Features within 77A1--77D1
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
(Dorer et al., 1995, Pauli et al., 1995, Roseman et al., 1995, Birchler et al., 1994, Castrillon et al., 1993)
Breakpoints

77A1;77D1

(Dorer et al., 1995, Pauli et al., 1995, Roseman et al., 1995, Castrillon et al., 1993)

77A1;77D

(Birchler et al., 1994)
Causes alleles
Carries alleles
cp1
(Kennison, 2006.7.21)
Transposon Insertions
Formalized genetic data

Su(Tpl) << bk1 << polo << fbl << bk2 << l(3)j7C3

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

Previously reported to delete cp, however this was due to Df(3L)rdgC-co2 chromosome carrying cp1. cp1 is separable from Df(3L)rdgC-co2 by recombination.

(Kennison, 2006.7.21)

All limits from polytene analysis (FBrf0064394)

Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
eRF1
(Collins and Cohen, 2005, Lukinova et al., 1999, Spradling et al., 1999, BDGP Project Members, 1994-1999)
fbl
(Spradling et al., 1999, BDGP Project Members, 1994-1999, Castrillon et al., 1993)
flc
(Lukinova et al., 1999)
in
(Lukinova et al., 1999, Adler et al., 1994)
l(3)77ABd
(Lukinova et al., 1999)
l(3)77ABf
(Lukinova et al., 1999)
l(3)77ABg
(Lukinova et al., 1999)
l(3)77ABh
(Lukinova et al., 1999)
l(3)77ABj
(Lukinova et al., 1999)
l(3)77CDa
(Lukinova et al., 1999)
l(3)77CDd
(Lukinova et al., 1999)
l(3)77CDe
(Lukinova et al., 1999)
l(3)77CDg
(Lukinova et al., 1999)
l(3)77CDh
(Lukinova et al., 1999)
l(3)77CDi
(Lukinova et al., 1999)
l(3)77CDj
(Lukinova et al., 1999)
l(3)77CDk
(Lukinova et al., 1999)
l(3)77CDl
(Lukinova et al., 1999)
l(3)77CDm
(Lukinova et al., 1999)
l(3)CMV45
(Slack et al., 2006)
l(3)S126014
(Szeged Stock Center, 1998-)
mRpL15
(Lukinova et al., 1999)
polo
(Lukinova et al., 1999, Spradling et al., 1999, Herrmann et al., 1998, Szeged Stock Center, 1998-, Roseman et al., 1995, BDGP Project Members, 1994-1999)
Prim2
(Chen et al., 2000, Lukinova et al., 1999, Spradling et al., 1999, BDGP Project Members, 1994-1999)
Psn
(Lukinova et al., 1999, Ye et al., 1999)
Pss
(Lukinova et al., 1999, Spradling et al., 1999, BDGP Project Members, 1994-1999)
Spn77Ba
(Lukinova et al., 1999)
trbl
(Großhans and Wieschaus, 2000, Mata et al., 2000, Seher, 2000.3.3)
αSnap
(Lukinova et al., 1999)
Partially deleted / disrupted
Molecular Data
Completely deleted
eRF1
(Marygold et al., 2007)
mRpL15
(Marygold et al., 2007)
Partially deleted
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

    Df(3L)rdgC-co2/Df(3L)ri-79c embryos show a failure to form a ventral furrow. The mesoderm primordium is internalised late.

    (Seher and Leptin, 2000)
    NOT in combination with other aberrations

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

    (Marygold et al., 2007)

    The Df(3L)rdgC-co2 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)rdgC-co2 results in 2.3% X chromosome nondisjunction and 3.4% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.

    (Harris et al., 2003)

    Homozygous mutants embryos show a failure to form a ventral furrow. The mesoderm primordium is internalised late.

    (Seher and Leptin, 2000)

    Does not cause unconditional lethality 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)

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

    (Pauli et al., 1995)
    Stocks (3)
    Notes on Origin
    Discoverer
     

    Induced on: marked third chromosome that carried the cp1 allele.

    (Kennison, 2006.7.21)
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (12)
    References (66)