FB2022_02, released March 29, 2022

Aberration: Dmel\Df(3L)vin7

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General Information
Symbol
Df(3L)vin7
Species
D. melanogaster
Name
Deficiency (3L) vin
FlyBase ID
FBab0002460
Feature type
chromosomal_deletion
Also Known As
Df(3L)vin7, vin7
Computed Breakpoints include

68C8;69B4-69B5

Features within 68C8--69B5
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
gamma ray
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Mogila, 1998.3.19, Deak et al., 1997, Duffy et al., 1996, Harbecke and Lengyel, 1995, Pauli et al., 1995, Jurgens et al., 1984)
Breakpoints

68C8-68C12;69B3-69C1

(Jurgens et al., 1984)

68C8-68C11;69B4-69B5

(Mogila, 1998.3.19, Deak et al., 1997, Duffy et al., 1996, Harbecke and Lengyel, 1995, Pauli et al., 1995)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

l(3)68Ca << bk1 << l(3)68Cb << l(3)69Ae << bk2 << gv

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

Ref: Akam et al., 1978, Cell 13: 215--225

(Jurgens et al., 1984)

Left limit of break 1 from polytene analysis (FBrf0041709) Right limit of break 1 from inclusion of rt (FBrf0031168) Limits of break 2 from polytene analysis (FBrf0080317)

Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
app
(Hoogwerf et al., 1988)
byn
(Kispert et al., 1994)
CycA
(Spradling et al., 1999, Szeged Stock Center, 1998-, Deak et al., 1997, BDGP Project Members, 1994-1999, Smith et al., 1993, Hoogwerf et al., 1988)
E(ftz)1427
(Kankel et al., 2004)
Est-6
(Hoogwerf et al., 1988)
l(3)68Cb
(Crosby and Meyerowitz, 1986)
l(3)68Cc
(Crosby and Meyerowitz, 1986)
l(3)68Cd
(Hoogwerf et al., 1988)
l(3)68Ce
(Hoogwerf et al., 1988)
l(3)68Cf
(Hoogwerf et al., 1988)
l(3)68Cg
(Hoogwerf et al., 1988)
l(3)68Ch
(Hoogwerf et al., 1988)
l(3)68Da
(Hoogwerf et al., 1988)
l(3)68Db
(Hoogwerf et al., 1988)
l(3)68Dc
(Hoogwerf et al., 1988)
l(3)68Eb
(Hoogwerf et al., 1988)
l(3)68Ec
(Hoogwerf et al., 1988)
l(3)68Ed
(Hoogwerf et al., 1988)
l(3)68Ee
(Hoogwerf et al., 1988)
l(3)68Ef
(Hoogwerf et al., 1988)
l(3)68Eg
(Hoogwerf et al., 1988)
l(3)68Fa
(Hoogwerf et al., 1988)
l(3)68Fb
(Hoogwerf et al., 1988)
l(3)68Fc
(Hoogwerf et al., 1988)
l(3)68Fd
(Hoogwerf et al., 1988)
l(3)68Fe
(Hoogwerf et al., 1988)
l(3)69Aa
(Hoogwerf et al., 1988)
l(3)69Ab
(Hoogwerf et al., 1988)
l(3)69Ac
(Hoogwerf et al., 1988)
l(3)69Ad
(Hoogwerf et al., 1988)
l(3)69Ae
(Hoogwerf et al., 1988)
l(3)69Af
(Hoogwerf et al., 1988)
l(3)69Ag
(Hoogwerf et al., 1988)
l(3)69Ba
(Hoogwerf et al., 1988)
l(3)69Bb
(Hoogwerf et al., 1988)
l(3)69Bc
(Hoogwerf et al., 1988)
l(3)69Bd
(Hoogwerf et al., 1988)
l(3)05088
(Spradling et al., 1999, BDGP Project Members, 1994-1999)
l(3)S004624
(Szeged Stock Center, 1998-, Deak et al., 1997)
l(3)S015012
(Deak et al., 1997)
l(3)S044626
(Deak et al., 1997)
l(3)S059913a
(Deak et al., 1997)
l(3)S081003
(Szeged Stock Center, 1998-, Deak et al., 1997)
l(3)S082106
(Szeged Stock Center, 1998-)
l(3)S093108a
(Deak et al., 1997)
l(3)S099312
(Szeged Stock Center, 1998-)
l(3)S100209
(Szeged Stock Center, 1998-)
l(3)S119715
(Szeged Stock Center, 1998-, Deak et al., 1997)
l(3)S132802b
(Deak et al., 1997)
l(3)S135710
(Szeged Stock Center, 1998-)
l(3)S145710a
(Deak et al., 1997)
l(3)S148214
(Deak et al., 1997)
Lsp2
(Hoogwerf et al., 1988)
ND-SGDH
(Spradling et al., 1999, BDGP Project Members, 1994-1999)
Nrx-IV
(Hoogwerf et al., 1988)
pag
(Riparbelli et al., 2005)
rols
(Spradling et al., 1999, BDGP Project Members, 1994-1999)
rt
(Hoogwerf et al., 1988, Crosby and Meyerowitz, 1986, Akam et al., 1978)
Su(hh)IV
(Haines and van Den Heuvel, 2000)
vers
(Spradling et al., 1999, BDGP Project Members, 1994-1999)
vin
(Hoogwerf et al., 1988, Crosby and Meyerowitz, 1986)
Partially deleted / disrupted
Molecular Data
Completely deleted
Pi3K68D
(MacDougall et al., 2004)
RpL10Ab
(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
    Phenotypic Data
    In combination with other aberrations

    Lethal in combination with Df(3L)BSC120. Inferred to overlap with: Df(3L)BSC120.

    (Andrade and Cook, 2005.7.22)
    NOT in combination with other aberrations

    Stage 15-16 mutant embryos form a single midgut chamber which is encircled by a thin sheet of visceral muscles. Hindgut development is incomplete.

    (Wolfstetter et al., 2009)

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

    (Marygold et al., 2007)

    Df(3L)vin7 embryos show defects in tracheal cell migration.

    (Myat et al., 2005)

    The Df(3L)vin7 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)vin7 results in 7.2% X chromosome nondisjunction and 3.6% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.

    (Harris et al., 2003)

    The level of 7-monoenes is normal in heterozygous males. The level of 7,11-dienes is significantly increased in heterozygous females compared to controls.

    (Wicker-Thomas and Jallon, 2000)

    No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.

    (Halsell and Kiehart, 1998)

    Shows no maternal enhancement of dpphr4.

    (Nicholls and Gelbart, 1998)

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

    (Duffy et al., 1996)

    Deficient embryos show a mutant midgut phenotype: no constrictions form, midgut epithelium is thin and fragile.

    (Bilder and Scott, 1995)

    Homozygous embryos have reduced anal pads. Midgut constrictions do not form, the hindgut is shorter than normal and Malpighian tubules form short buds.

    (Harbecke and Lengyel, 1995)

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

    (Pauli et al., 1995)

    Fertile when heterozygous with haync2.

    (Regan and Fuller, 1988)
    Stocks (2)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (9)
    References (69)