A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Aberration Dmel\Dp(1;2)51b

General Information
SymbolDmel\Dp(1;2)51bSpeciesD. melanogaster
NameFlyBase IDFBab0009100
Feature typeinterchromosomal_duplicationCreated / Updated2006-08-22/2006-08-22
Formalized genetic data
Sequence coordinates
Deleted segment
Duplicated segment3C2--3D6
Computed Breakpoints include
Breakpoints Inherited  
hide Nature of the Aberration
Cytological Order
Progenitor
Tp(1;2)w51b
 
Mutagen
segregation
 
Class of aberration (relative to progenitor)
unoriented_insertional_duplication
 
Breakpoints
Causes alleles
Carries alleles
Transposon Insertions
Genetic mapping information
Comments
hide Comments on Cytology
Duplication for the X chromosome region w+, rst+ through N+ to dm+ inserted into the second chromosome.
(Welshons and Welshons, 1986)
hide Molecularly Mapped Breakpoints
 
hide Sequence Crossreferences
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
hide Gene Deletion & Duplication Data
hide Genes Deleted / Disrupted
Complementation Data
Molecular Data
hide Genes NOT Deleted / Disrupted
Complementation Data
Molecular Data
hide Genes Duplicated
Complementation Data
Completely duplicated
w
(Lefevre and Wilkins, 1966, Welshons, 1974, Zachar and Bingham, 1982, Poulson and Lefevre, 1982, Bingham and Zachar, 1985, Welshons and Welshons, 1986, Judd, 1995)
N
(Lefevre and Wilkins, 1966, Lefevre and Peterson, 1972, Welshons, 1974, Poulson and Lefevre, 1982, Kramers et al., 1983, Welshons and Welshons, 1986, Kramers et al., 1991, Dambly-Chaudiere and Leyns, 1992, de Celis et al., 1993, de Celis and Garcia-Bellido, 1994, Johnson et al., 1995, Matsuno et al., 1995, Judd, 1995, Leviten and Posakony, 1996)
dnc
(Levine et al., 1994)
dm
(Welshons, 1974, Poulson and Lefevre, 1982, Kramers et al., 1983, Welshons and Welshons, 1986, Kramers et al., 1991, Judd, 1995)
rst
(Lefevre and Wilkins, 1966, Poulson and Lefevre, 1982, Kramers et al., 1983, Kramers et al., 1991, Judd, 1995)
l(1)3Da
(Kramers et al., 1983, Kramers et al., 1991)
l(1)3Db
(Vervoort et al., 1997)
Partially duplicated
rst
(Welshons and Welshons, 1986)
Molecular Data
hide Genes NOT Duplicated
Complementation Data
Actn
(Kramers et al., 1991)
Pgd
(Kramers et al., 1991)
pn
(Kramers et al., 1991)
phl
(Kramers et al., 1991)
crn
(Kramers et al., 1991)
kz
(Kramers et al., 1991)
wapl
(Kramers et al., 1991)
wds
(Kramers et al., 1991)
egh
(Kramers et al., 1991)
tko
(Kramers et al., 1991)
gt
(Kramers et al., 1991)
sgg
(Kramers et al., 1991)
dwg
(Kramers et al., 1983, Kramers et al., 1991)
w
(Kramers et al., 1983, Kramers et al., 1991)
crm
(Kramers et al., 1983, Kramers et al., 1991)
trol
(Kramers et al., 1991)
z
(Kramers et al., 1991)
mit(1)15
(Kramers et al., 1991)
l(1)air3
(Watson et al., 1991)
l(1)air4
(Watson et al., 1991)
l(1)air5
(Watson et al., 1991)
l(1)air6
(Watson et al., 1991)
l(1)3Ah
(Kramers et al., 1991)
l(1)2Dk
(Kramers et al., 1991)
l(1)3Al
(Kramers et al., 1991)
l(1)EA65
(Kramers et al., 1983, Kramers et al., 1991)
l(1)3Ed
(Kramers et al., 1983, Kramers et al., 1991)
l(1)3-64
(Kramers et al., 1983, Kramers et al., 1991)
l(1)3Bb
(Kramers et al., 1983, Kramers et al., 1991)
l(1)3Bf
(Kramers et al., 1983, Kramers et al., 1991)
l(1)3Ao
(Kramers et al., 1991)
l(1)2Dj
(Kramers et al., 1991)
l(1)ESHS14
(Kramers et al., 1991)
l(1)2Ff
(Kramers et al., 1991)
l(1)2Ea
(Kramers et al., 1991)
l(1)3Eb
(Kramers et al., 1983, Kramers et al., 1991)
l(1)3Aj
(Kramers et al., 1991)
l(1)2Fg
(Kramers et al., 1991)
l(1)2Dm
(Kramers et al., 1991)
l(1)3Ap
(Kramers et al., 1991)
l(1)2Fd
(Kramers et al., 1991)
l(1)7-103
(Kramers et al., 1983, Kramers et al., 1991)
l(1)3Bg
(Kramers et al., 1991)
l(1)3ABa
(Kramers et al., 1991)
l(1)3Am
(Kramers et al., 1991)
l(1)2Fc
(Kramers et al., 1991)
l(1)2Dl
(Kramers et al., 1991)
l(1)3Bd
(Kramers et al., 1983, Kramers et al., 1991)
l(1)2Ed
(Kramers et al., 1991)
l(1)3ABb
(Kramers et al., 1991)
l(1)3Ak
(Kramers et al., 1991)
l(1)3Aq
(Kramers et al., 1991)
l(1)2Fb
(Kramers et al., 1991)
l(1)3An
(Kramers et al., 1991)
l(1)2Ec
(Kramers et al., 1991)
l(1)3Bc
(Kramers et al., 1983, Kramers et al., 1991)
Molecular Data
hide Related Comments
Does not fully cover the rst6 phenotype; Dp(1;2)51b/rst6 flies have a fine, evenly distributed roughness that very closely approximates wild-type.
(Welshons and Welshons, 1986)
hide Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations
Chromosome in combination with sno1 exhibits near wild type phenotype (small deltas remain, there is some thoracic hairiness and the eyes are not completely smooth): mutant phenotype is suppressed.
(Lefevre and Peterson, 1972)
Flies carrying two copies of Dp(1;2)51b in an otherwise wild-type background have a wing phenotype indistinguishable from that of DlM1/+ heterozygotes. This phenotype is enhanced by DlM1.
(de Celis and Bray, 2000)
Heterozygotes exhibit a thickened vein phenotype.
(Matsuno et al., 1995)
Three wild type copies of N suppresses the Brd1 and Brd3 bristle multiplication phenotype.
(Leviten and Posakony, 1996)
Transheterozygotes with aopA141 or aoppok-x8 exhibit enhancement of the rough eye phenotype.
(Rogge et al., 1995)
hide Position Effect Variegation Data
Genes NOT subject to PEV
N
(Lefevre and Wilkins, 1966)
rst
(Lefevre and Wilkins, 1966)
w
(Lefevre and Wilkins, 1966)
hide Stocks ( 12 )
Bloomington
937
Df(1)N-71h/C(1)M3, y2; Dp(1;2)51b/+
6894
Df(1)N-54l9, y1/C(1)DX, y1 w1 f1; Dp(1;2)51b/+
3015
N55e11 rb1/C(1)DX, y1 w1 f1; Dp(1;2)51b/+
3006
Df(1)N-81k1, dnc81k1/C(1)DX, y1 w1 f1; SM1, Dp(1;2)51b/+
2211
wa NCo rb1/C(1)DX, y1 w1 f1; Dp(1;2)51b/+
938
Df(1)N-69h9, dnc69h9 rb1/C(1)DX, y1 w1 f1; Dp(1;2)51b/+
Kyoto
106134
Df(1)N-71h/C(1)M3, y2; Dp(1;2)51b/+
106784
N55e11 rb1/C(1)DX, y1 w1 f1; Dp(1;2)51b/+
107522
Df(1)N-81k1, dnc81k1/C(1)DX, y1 w1 f1; SM1, Dp(1;2)51b/+
106743
wa NCo rb1/C(1)DX, y1 w1 f1; Dp(1;2)51b/+
101861
wa NCo rb1 / C(1)DX, y1 w1 f1 ; Dp(1;2)51b / +
106135
Df(1)N-69h9, dnc69h9 rb1/C(1)DX, y1 w1 f1; Dp(1;2)51b/+
hide Notes on Origin
Discoverer
hide Balancer / Genotype Variants of the Aberration
    hide Separable Components
      hide Other Comments
      Duplication is viable and used to cover lethality of N in studies of pseudoallelism at the N locus (FBrf0014640).
       
      hide Synonyms & Secondary IDs ( 15 )
      Reported As
      Symbol Synonym
      Dp51b7
      (Lefevre, 1974, Kramers et al., 1991, Kramers et al., 1983)
      Dp(1,2)51b
      (Palka et al., 1990)
      Dp(1,2)w+51b7
      (Bingham and Zachar, 1985)
      Dp(1;2)51b
      (Acar et al., 2008)
      Dp(1;2)51b7
      (Vervoort et al., 1997, Artavanis-Tsakonas et al., 1983, Welshons, 1974, Gorman and Girton, 1992)
      Dp(1;2)+51b7
      (Artavanis-Tsakonas et al., 1983)
      Dp(1;2)w51b7
      (Gersh, 1967)
      Dp(1;2)w51b
       
      Dp(1;2)w+51b7
      (de Celis and Bray, 2000, Jacobsen et al., 1998, Leviten and Posakony, 1996, Dambly-Chaudiere and Leyns, 1992, Matsuno et al., 1995, Lefevre and Green, 1972, de Celis and Garcia-Bellido, 1994, Zachar and Bingham, 1982, Watson et al., 1991, de Celis et al., 1993, )
      Dp(1;2)w+51b
      (de Celis and Garcia-Bellido, 1994, Reuter et al., 1985)
      Dp(1;2)w+51b7
      (Rogge et al., 1995, Clark et al., 1994, )
      Dp(1;2R)w+51b7
      (Lefevre and Wilkins, 1966)
      Dp(N+)
      (Rogge et al., 1995)
      DpN+
      (de Celis and Bray, 2000)
      Dp w+51b7
      (Lefevre, 1968, Green, 1959, Lefevre and Peterson, 1972)
      Name Synonym
      Secondary FlyBase IDs
        hide References ( 43 )
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        hide Recent research papers ( 1 )
        Acar et al., 2008, Cell 132(2): 247--258
        Rumi is a CAP10 domain glycosyltransferase that modifies Notch and is required for Notch signaling. [FBrf0204793]
        Show all research papers ...