FB2024_04 , released June 25, 2024
Aberration: Dmel\Df(1)v-L15
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General Information
Symbol
Df(1)v-L15
Species
D. melanogaster
Name
Deficiency (1) vermilion
FlyBase ID
FBab0000984
Feature type
chromosomal_deletion
Also Known As
Df(1)vL15, Df(1)v-L15, vl15
Computed Breakpoints include

9B1;10A1

Features within 9B1--10A1
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
X ray
(Lefevre, 1969)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Duffy et al., 1996, Harbecke and Lengyel, 1995, Pauli et al., 1995, Prudhommeau and Proust, 1990, Perrimon et al., 1989, Eberl and Hilliker, 1988, Deak et al., 1982, Mason et al., 1981, Craymer and Roy, 1980, Lefevre, 1969)
Breakpoints

9B1;10A1

(Prudhommeau and Proust, 1990, Perrimon et al., 1989, Eberl and Hilliker, 1988, Deak et al., 1982, Mason et al., 1981, Craymer and Roy, 1980, Lefevre, 1969)

9B1-9B2;10A1-10A2

(Duffy et al., 1996, Harbecke and Lengyel, 1995, Pauli et al., 1995)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

Yp1 << bk1 << l(1)75B5 << bk2 << sev

Genetic mapping information
Comments
Comments on Cytology

Limits of break 1 from polytene analysis (FBrf0020605) Left limit of break 2 from inclusion of csk (FBrf0035977) Right limit of break 2 from polytene analysis (FBrf0020605)

Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Genes NOT Deleted / Disrupted
Complementation Data
 
cac
(Eeken et al., 1985)
dlg1
(Zhimulev et al., 1987)
Dna2
(Mason et al., 1981, Baker and Smith, 1979)
dsh
(Zhimulev et al., 1987, Zhimulev et al., 1981)
Fs(1)10A
(Zhimulev et al., 1987)
hop
(Hanratty and Dearolf, 1993, Zhimulev et al., 1987, Eeken et al., 1985)
Hsp60A
(Kozlova et al., 1994, Zhimulev et al., 1987, Zhimulev et al., 1981)
l(1)7B
(Eeken, 1982)
l(1)10Ad
(Kozlova et al., 1994, Zhimulev et al., 1987, Zhimulev et al., 1981)
l(1)10Ae
(Kozlova et al., 1994, Zhimulev et al., 1987, Zhimulev et al., 1981)
l(1)10Af
(Zhimulev et al., 1987)
l(1)10Ba
(Zhimulev et al., 1987)
l(1)10Bb
(Zhimulev et al., 1987)
l(1)10Bc
(Zhimulev et al., 1987)
l(1)10Bg
(Zhimulev et al., 1987)
l(1)10Bh
(Zhimulev et al., 1987)
l(1)10Bm
(Zhimulev et al., 1987)
l(1)10Cc
(Eeken et al., 1985)
l(1)10Fg
(Eeken et al., 1985)
l(1)11A
(Eeken, 1982)
l(1)11Ae
(Eeken et al., 1985)
l(1)48B
(Eeken, 1982)
l(1)75B1
(Eeken, 1982)
l(1)75B2
(Eeken, 1982)
l(1)75B3
(Eeken, 1982)
l(1)75B4
(Eeken, 1982)
l(1)89B
(Eeken, 1982)
l(1)ESHS40
(Eeken et al., 1985)
l(1)ESHS44
(Eeken et al., 1985)
l(1)ESHS45
(Eeken et al., 1985)
l(1)ESHS46
(Eeken et al., 1985)
m
(Eeken et al., 1985)
mei-41
(Mason et al., 1981)
ms(1)10A
(Kozlova et al., 1994, Zhimulev et al., 1987, Zhimulev et al., 1981)
mus101
(Mason et al., 1981)
mw
(Birchler et al., 1989)
nej
(Florence and McGinnis, 1998)
ny
(Zhimulev et al., 1987)
PCNA
(Schalet, 1986)
Polr2A
(Eeken et al., 1985)
rtv
(Zhimulev et al., 1987, Eeken et al., 1985, Zhimulev et al., 1981)
sev
(Kozlova et al., 1994, Zhimulev et al., 1987, Zhimulev et al., 1981)
slm10A
(Kozlova et al., 1994, Zhimulev et al., 1987, Zhimulev et al., 1981)
tu(1)Sz
(Zhimulev et al., 1987)
Yp1
(Minoo and Postlethwait, 1985)
Molecular Data
 
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

    Df(1)v-L15 does not rescue the weakly viable D.melanogaster/D.simulans hybrid females derived from a cross of D.simulans females to D.melanogaster males.

    (Orr and Irving, 2000)

    Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.

    (Coyne et al., 1998)

    Intermediate second site non-complementing phenotype with zipEbr and zipmhc-c6.1 : malformed phenotype penetrance 25-75%.

    (Halsell and Kiehart, 1998)

    Dominantly causes tergite defects in less than 50% of run3 heterozygotes.

    (Duffy et al., 1996)

    Deficient embryos show a variably penetrant mutant midgut phenotype: incomplete constriction formation.

    (Bilder and Scott, 1995)

    Homozygous embryos do not complete head involution, and tracheae are disconnected. Fusion of the midgut primordia and elongation of the hindgut and Malpighian tubules is variable.

    (Harbecke and Lengyel, 1995)

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

    (Pauli et al., 1995)

    Hemizygous embryos were examined with polarised light microscopy and antibody staining: muscle pattern incomplete due to muscle absences.

    (Drysdale et al., 1993)
    Stocks (5)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    flw alleles are lethal over Df(1)v-L15 but viable over Df(1)C52, with a flap-wing phenotype.

    (Deak et al., 1982)
    Synonyms and Secondary IDs (15)
    References (46)