A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(3R)red1

General Information
SymbolDmel\Df(3R)red1SpeciesD. melanogaster
NameDeficiency (3R) red Malpighian tubulesFlyBase IDFBab0002877
Feature typechromosomal_deletion
Also Known AsDf(3R)red1
Computed Breakpoints include [<88A2];88C1--D1
Deleted segment88A2--88D1
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
88B1;88D2-88D3
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data bk1 << cash << bk2 << put
Genetic mapping information
Comments
hide Comments on Cytology
Right limit of break 1 from inclusion of ems (FBrf0049810) Left limit of break 2 from inclusion of l(3)06951 (FBrf0067338) Right limit of break 2 from non-inclusion of l(3)03719 (FBrf0067338)
 
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DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
hide Gene Deletion & Duplication Data
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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
Homozygotes for Df(3R)red1 fail to hatch.
The Df(3R)red1 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).
Heterozygosity for Df(3R)red1 results in 1.6% X chromosome nondisjunction and 0.6% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Midgut development of mutant embryos is wild type.
Heterozygosity for this deletion enhances the mutant ovarian phenotype of ovoD2.
Df(3R)red/+ progeny of Df(1)C128/+ females show a high frequency of homeotic transformations (Gans et al., 1980).
 
hide Stocks ( 2 )
Bloomington
Kyoto
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Discoverer
hide Balancer / Genotype Variants of the Aberration
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hide Synonyms & Secondary IDs ( 4 )
Reported As
Symbol Synonym
Df(3R)red1
Name Synonym
Deficiency (3R) red Malpighian tubules
 
Secondary FlyBase IDs
hide References ( 28 )
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All research papers listed in FlyBase were published before 2011