FB2024_04 , released June 25, 2024
Aberration: Dmel\Df(3L)BSC13
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General Information
Symbol
Df(3L)BSC13
Species
D. melanogaster
Name
FlyBase ID
FBab0029723
Feature type
chromosomal_deletion
Computed Breakpoints include
Features within 66B12--66D4
Sequence coordinates
Member of large scale dataset(s)
Dfs_BSC_set1

A set of ~50 targeted deficiencies created by exploiting hybrid element insertion (HEI) and resolution; designed to fill gaps in deletion coverage.

(Parks et al., 2004)
Nature of Aberration
Cytological Order
Progenitor
P{lacW}Nmtj1C7
(Parks et al., 2004, Deal and Cook, 2002.2.25)
P{EP}ergic53EP3212
(Parks et al., 2004, Deal and Cook, 2002.2.25)
Mutagen
Delta2-3 transposase
(Deal and Cook, 2002.2.25)
recombination
(Deal and Cook, 2002.2.25)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Parks et al., 2004, Deal and Cook, 2002.2.25)
Breakpoints

66B12-66C14;66D2-66D4

(Deal and Cook, 2002.2.25)

66B12-66C1;66D2-66D4

(Parks et al., 2004)
Causes alleles
Carries alleles
e1
(Deal and Cook, 2002.2.25)
rhove-1
(Deal and Cook, 2002.2.25)
Transposon Insertions
Formalized genetic data
Genetic mapping information
Comments
Comments on Cytology
Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
Gug
(Deal and Cook, 2002.2.25)
l(3)B27
(Slack et al., 2006)
Partially deleted / disrupted
Molecular Data
Completely deleted
eIF4E3
(Marygold et al., 2007)
Partially deleted
Genes NOT Deleted / Disrupted
Complementation Data
 
MED24
(Wang et al., 2008)
rhea
(Levi et al., 2006)
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

    Lethal in combination with T(2;3)E(da).

    (Deal and Cook, 2002.2.25)
    NOT in combination with other aberrations

    The distal half of the salivary gland turns but the proximal half does not in embryos homozygous for Df(3L)BSC13 by stage 14.

    (Jattani et al., 2009)

    The Df(3L)BSC13 chromosome acts as a dominant weak 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)BSC13 results in 50.8% X chromosome nondisjunction and 11.9% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.

    (Harris et al., 2003)
    Stocks (1)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    The miniwhite markers from both P{lacW}Nmtj1C7 and P{EP}ergic53EP3212 were deleted or disrupted.

    (Mason, 2004.11.26)
    Synonyms and Secondary IDs (1)
    References (16)