A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Aberration Dmel\In(2LR)Px4

General Information
SymbolDmel\In(2LR)Px4SpeciesD. melanogaster
NameInversion (2LR) PlexateFlyBase IDFBab0004789
Feature typechromosomal_inversionCreated / Updated2006-08-22/2006-08-22
Formalized genetic data
Sequence coordinates
Deleted segment
Duplicated segment
Computed Breakpoints include
Breakpoints Inherited  
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Cytological Order
2Lt - 22A3 | 60B - 58B1 | 42A3 - 58A4 | 42A2 - 21D1 | 60D2 - 2Rt
 
Progenitor
Mutagen
Class of aberration (relative to progenitor)
Breakpoints
Causes alleles
Carries alleles
Transposon Insertions
Genetic mapping information
Comments
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Inverted for 60B8-60B10;60D1
Deficient for 60B-60C;60D1-60D2
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DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
hide Gene Deletion & Duplication Data
hide Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
 
 
Molecular Data
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Complementation Data
Molecular Data
hide Genes Duplicated
Complementation Data
Completely duplicated
 
Molecular Data
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Complementation Data
Molecular Data
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In combination with other aberrations
NOT in combination with other aberrations
Heterozygotes have a blistered wing and ectopic vein phenotype.
Heterozygotes with T(2;3)God1 are inviable.
Homozygotes die at the beginning of the first larval instar stage because the larvae cannot exit from the chorion. The larvae are deformed with stunted growth. The sclerotised mouthparts and denticle belts develop normally.
Intermediate second site non-complementing phenotype with zipEbr and zipmhc-c6.1: malformed phenotype penetrance 25-75%.
Midgut development of mutant embryos is wild type.
Progeny of the genotype zip/Df(zip) exhibit the mlf phenotype (malformed syndrome), wing malformations and leg defects, at a penetrance of 14--35%.
Shows a haploinsufficient ectopic wing vein phenotype.
Shows no maternal enhancement of dpphr4.
The tracheal phenotypes previously reported for this deficiency in FBrf0051997 and FBrf0072461, where the primary branches are disrupted and discontinuous, are due to the deletion of a gene other than bs, or more than one gene in the region.
Wing venation phenotype like Df(2R)Px1. Thickening of L5 at posterior crossvein produces a vesicle, as in bs. More extreme in female. homozygous lethal
 
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hide Stocks ( 3 )
Bloomington
Kyoto
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Discoverer
Thompson, June 1956, 1957.
 
A recurrent product of recombination in region 33F-40F between In(2LR)21C8-D1;60D1-2 from In(2LR)bwV1 [In(2LR)21C8-D1;60D1-2 + In(2LR)40F;59D4-E1] and In(2LR)22A3-B1;60B-C from SM1 [In(2L)Cy = In(2L)22D1-2;33F5-34A1 + In(2LR)22A3-B1;60B-C + In(2R)Cy = In(2R)42A2-3;58A4-B1].
 
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      hide Other Comments
      "Deletes or disrupts sp" was stated as tentative. The reciprocal recombinant is In(2LR)S56f.
       
      hide Synonyms & Secondary IDs ( 13 )
      Reported As
      Symbol Synonym
      Df(2R)Px4,Dp(2L)
      Df(2R)Px[4]
      Dp(2;2)S56f
       
      In(2LR)Px4
       
      Name Synonym
      Inversion (2LR) Plexate
       
      Secondary FlyBase IDs
      • FBab0004790
      • FBab0003501
      hide References ( 37 )
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      hide Recent research papers ( 1 )
      Crest et al., 2007, Genetics 175(2): 567--584
      Onset of the DNA replication checkpoint in the early Drosophila embryo. [FBrf0194644]