A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Aberration Dmel\Df(1)RA47

General Information
SymbolDmel\Df(1)RA47SpeciesD. melanogaster
NameFlyBase IDFBab0000665
Feature typechromosomal_deletionCreated / Updated2006-08-22/2006-08-22
Formalized genetic data dy << bk1 << l(1)10Fe << pot << bk2 << cac
Sequence coordinates
Deleted segment10F1--10F10
Duplicated segment
Computed Breakpoints include 10F1;10F10
Breakpoints Inherited  
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Cytological Order
Progenitor
Mutagen
 
Class of aberration (relative to progenitor)
Breakpoints
Causes alleles
Carries alleles
Transposon Insertions
Genetic mapping information
Comments
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Limits of break 1 from polytene analysis (FBrf0034402) Left limit of break 2 from polytene analysis (FBrf0040178) Right limit of break 2 from polytene analysis (FBrf0054499)
 
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DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
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Complementation Data
Completely deleted / disrupted
Molecular Data
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Complementation Data
Molecular Data
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Complementation Data
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
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Heterozygous oocytes have a higher frequency of meiosis I figures in which chromosomes are initiating separation than wild-type oocytes. The behaviour of the separated chromosomes is usually normal.
No significant change in female lethality when in combination with Sxlf1.
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Bloomington
Kyoto
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Discoverer
Lefevre.
 
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      Reported As
      Symbol Synonym
      Name Synonym
      Secondary FlyBase IDs
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        All research papers listed in FlyBase were published before 2006