A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(1)C246

General Information
SymbolDmel\Df(1)C246SpeciesD. melanogaster
NameFlyBase IDFBab0000355
Feature typechromosomal_deletion
Also Known AsC246
Computed Breakpoints include 11D1;12A1
Deleted segment11D1--12A1
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
11;12A1-12A2
11D-11E;12A1
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data gs(1)N41 << bk1 << l(1)11Dc << Gpt << bk2 << up
Genetic mapping information
Comments
hide Comments on Cytology
Left limit of break 1 from polytene analysis (citation unavailable) Right limit of break 1 from inclusion of rad (FBrf0053305) Left limit of break 2 from polytene analysis (FBrf0034402) Right limit of break 2 from polytene analysis (FBrf0086390)
 
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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
hide Genes NOT Deleted / Disrupted
Complementation Data
Molecular Data
hide Genes Duplicated
Complementation Data
Molecular Data
hide Genes NOT Duplicated
Complementation Data
Molecular Data
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hide Phenotypic Data
In combination with other aberrations
YSX.YL, Df(1)C246, In(1)EN, y M/C(1;Y)2, Df(1)gl In(1)EN, y g f B females are viable, yellow and Minute (Schalet).
 
NOT in combination with other aberrations
Shows dominant enhancement of dominant haltere phenotype caused by Ubx195 and Ubx9.22.
Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.
No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.
Shows no maternal enhancement of dpphr4.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Deficient embryos show an uninterpretable mutant midgut phenotype.
Heterozygosity for this deletion suppresses the mutant ovarian phenotype of ovoD2.
Hemizygous embryos were examined with polarised light microscopy and antibody staining: muscle pattern incomplete due to muscle absences and detachments.
Mutants show a moderate Minute phenotype.
hide Stocks ( 2 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
Lefevre.
 
hide Balancer / Genotype Variants of the Aberration
hide Separable Components
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hide Synonyms & Secondary IDs ( 6 )
Reported As
Symbol Synonym
Df(2L)C246
Name Synonym
Secondary FlyBase IDs
hide References ( 46 )
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All research papers listed in FlyBase were published before 2011