FB2025_01 , released February 20, 2025
Aberration: Dmel\Df(2R)stan2
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General Information
Symbol
Df(2R)stan2
Species
D. melanogaster
Name
FlyBase ID
FBab0024382
Feature type
chromosomal_deletion
Computed Breakpoints include

46F1;47B9

Features within 46F1--47B9
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
X ray
(Roote, 1996.4.17)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Zhimulev et al., 1998, Zhimulev et al., 1997.9.29, Roote, 1996.4.17)
Breakpoints

46F1-46F2;47D1-47D2

(Roote, 1996.4.17)

46F1;47B9

(Zhimulev et al., 1998, Zhimulev et al., 1997.9.29)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data
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

Left limit of break 1 from polytene analysis (FBrf0086743) Right limit of break 1 from polytene analysis (FBrf0098597) 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
Complementation Data
 
14-3-3ζ
(Goldstein et al., 2001)
Coprox
(BDGP Project Members, 1994-1999)
EG162
(Ma et al., 2009)
eIF3j
(Goldstein et al., 2001)
eve
(Goldstein et al., 2001)
Fpps
(Spradling et al., 1999, BDGP Project Members, 1994-1999)
Gαo
(BDGP Project Members, 1994-1999)
Jra
(Goldstein et al., 2001)
l(2)46CDa
(Goldstein et al., 2001)
l(2)46CFn
(Goldstein et al., 2001)
l(2)46Ci
(Goldstein et al., 2001)
l(2)46Cj
(Goldstein et al., 2001)
l(2)46Ck
(Goldstein et al., 2001)
l(2)46Cl
(Goldstein et al., 2001)
l(2)46Cm
(Goldstein et al., 2001)
l(2)46Cn
(Goldstein et al., 2001)
l(2)46Dh
(Goldstein et al., 2001)
l(2)46Di
(Goldstein et al., 2001)
l(2)46Dj
(Goldstein et al., 2001)
l(2)46Ea
(Goldstein et al., 2001)
l(2)46Eb
(Goldstein et al., 2001)
l(2)46Ed
(Goldstein et al., 2001, Spradling et al., 1999, BDGP Project Members, 1994-1999)
l(2)46Eg
(Goldstein et al., 2001)
l(2)46Ei
(Goldstein et al., 2001)
l(2)46Ej
(Goldstein et al., 2001)
l(2)46Fa
(Goldstein et al., 2001)
l(2)46Fb
(Goldstein et al., 2001)
l(2)00297
(BDGP Project Members, 1994-1999)
l(2)08685
(BDGP Project Members, 1994-1999)
l(2)gl
(Mason et al., 2004)
l(2)k00909
(BDGP Project Members, 1994-1999)
l(2)k03610
(Spradling et al., 1999, BDGP Project Members, 1994-1999)
l(2)k04308
(Spradling et al., 1999, BDGP Project Members, 1994-1999)
l(2)k07126
(BDGP Project Members, 1994-1999)
l(2)k15826
(BDGP Project Members, 1994-1999)
Mef2
(Goldstein et al., 2001)
S
(BDGP Project Members, 1994-1999)
shn
(Spradling et al., 1999, BDGP Project Members, 1994-1999)
TER94
(Goldstein et al., 2001)
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 (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
    NOT in combination with other aberrations

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

    (Marygold et al., 2007)

    Heterozygosity for Df(2R)stan2 results in 6.6% X chromosome nondisjunction and 10.9% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.

    (Harris et al., 2003)
    Stocks (3)
    Notes on Origin
    Discoverer

    G. Johnson

    (Roote, 1996.4.17)

    G. Johnson.

     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    The Df(2R)stan2 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), but this is a false positive result (the suppressor is not within the bounds of the deficient region) because the region of the deficiency is covered by a combination of nonsuppressing deficiencies and deficiencies with suppressors that map to the 2L tip.

    (Mason et al., 2004)

    "46F1;47B9" was stated as revision.

    (Zhimulev et al., 1998, Zhimulev et al., 1997.9.29)
    Synonyms and Secondary IDs (5)
    References (28)