A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Aberration Dmel\Df(3L)fz-D21

General Information
SymbolDmel\Df(3L)fz-D21SpeciesD. melanogaster
NameFlyBase IDFBab0002370
Feature typechromosomal_deletionCreated / Updated2006-08-22/2006-08-22
Formalized genetic data Hsc70Cb << bk1 << D << shd << bk2 << gnu
Sequence coordinates
Deleted segment70D2--70E8
Duplicated segment
Computed Breakpoints include 70D2;70E8
Breakpoints Inherited  
hide Nature of the Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to progenitor)
Breakpoints
70D1-70D2;70E7
Causes alleles
Carries alleles
Transposon Insertions
Genetic mapping information
Comments
hide Comments on Cytology
Left limit of break 1 from polytene analysis (FBrf0075380) Right limit of break 1 from inclusion of D (FBrf0075380) Limits of break 2 from polytene analysis (FBrf0075380)
 
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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
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Complementation Data
Molecular Data
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Complementation Data
Molecular Data
hide Related Comments
Does not delete P{lacW}endosS067006
hide Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations
Double mutants of fz21, fz23 or Df(3L)fz-D21 with Df(3L)fz2 show variable embryonic segmentation defects ranging from a few extra denticles in the posterior part of some segments to complete replacement of naked cuticle with denticles. This phenotype is reminiscent of that for P{en1}wgen11 loss of function.
Exhibit dominant suppression of Pc.
Heterozygosity for Df(3L)fz-D21 results in 1.1% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
No effect on the eye pigment phenotype of wT81.
Shows dominant enhancement of dominant haltere phenotype caused by Ubx195 and Ubx9.22.
Shows no maternal enhancement of dpphr4.
The Df(3L)fz-D21 chromosome does not act as a dominant 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).
hide Position Effect Variegation Data
  
hide Stocks ( 3 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
Adler.
 
hide Balancer / Genotype Variants of the Aberration
    hide Separable Components
      hide Other Comments
      "70D2;70E8" was stated as revision.
      hide Synonyms & Secondary IDs ( 7 )
      Reported As
      Symbol Synonym
      Df(3L)fz-D21
       
      Name Synonym
      Secondary FlyBase IDs
      • FBal0039358
      hide References ( 47 )
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      hide Recent research papers ( 1 )
      Shimada et al., 2006, Dev. Cell 10(2): 209--222
      Polarized transport of Frizzled along the planar microtubule arrays in Drosophila wing epithelium. [FBrf0190217]