A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(1)KA6

General Information
SymbolDmel\Df(1)KA6SpeciesD. melanogaster
NameFlyBase IDFBab0000484
Feature typechromosomal_deletion
Computed Breakpoints include 10E1;11A7
Deleted segment10E1--11A7
Sequence coordinates
Member of large scale dataset(s)
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Description
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FB2013_03
FB2013_02
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Nature of the Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to progenitor)
Breakpoints
10E1-10E2;11A6-11A9
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data Rst(1)JH << bk1 << l(1)10Fk << l(1)10Ea << bk2 << gs(1)N41
Genetic mapping information
Comments
Breakpoint(s) molecularly mapped
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Deletion of 22/24 bands.
All limits from polytene analysis (FBrf0034402)
 
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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
Completely deleted
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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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hide Phenotypic Data
In combination with other aberrations
Df(1)KA6/Df(1)m259-4 heterozygotes are viable.
Heterozygotes with Df(1)m259-4 survive and have an extreme m phenotype with flimsy wings.
NOT in combination with other aberrations
Df(1)KA6 hemizygous embryos exhibit head and thorax defects similar to tsg loss of function mutants. With a very low penetrance, Df(1)KA6 hemizygous embryos show subtle defects in segmentation, including partial fusion of denticle band pairs in the register seen for Ten-m mutants. Flies with transheterozygous combinations of Df(1)KA6/+ and Ten-m[628]/+ display eye roughness. Consistent features include ommatidial order defects, ommatidial fusions, eye sensory bristle loss, and occasional supernumerary sensory bristles.
Hemizygous late embryonic lethal.
Acts as a dosage sensitive maternal modifier of run: causes tergite defects in greater than 50% of run3 heterozygotes. Maternal heterozygosity for Df(1)KA6 greatly increases the frequency of segmentation defects in embryos heterozygous for eve, run and Kr.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
No significant change in female lethality when in combination with Sxlf1.
Heterozygous females exhibit reduced viability and fertility.
hide Stocks ( 2 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
Lefevre.
 
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hide Synonyms & Secondary IDs ( 3 )
Reported As
Symbol Synonym
Name Synonym
Secondary FlyBase IDs
hide References ( 29 )
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All research papers listed in FlyBase were published before 2011