A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(3R)Dl-BX12

General Information
SymbolDmel\Df(3R)Dl-BX12SpeciesD. melanogaster
NameDeficiency (3R) DeltaFlyBase IDFBab0002534
Feature typechromosomal_deletion
Also Known AsDf(3R)D1-BX12, Df(3R)DlBX12, Df(3R)DLBX12
Computed Breakpoints include 91F1-91F2;92D3-92D6
Deleted segment91F1--92D6
Sequence coordinates
Member of large scale dataset(s)
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Description
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FB2013_03
FB2013_02
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hide Nature of the Aberration
Cytological Order
Progenitor
Mutagen
 
Class of aberration (relative to progenitor)
Breakpoints
91F1-91F2;92D2-92D6
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data pros << bk1 << cdi << bwk << bk2
Genetic mapping information
Comments
hide Comments on Cytology
Limits of break 1 from polytene analysis (FBrf0080317) Left limit of break 2 from polytene analysis (FBrf0082073) Right limit of break 2 from polytene analysis (FBrf0080317)
 
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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
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In combination with other aberrations
NOT in combination with other aberrations
The distal half of the salivary gland turns but the proximal half does not in embryos homozygous for Df(3R)Dl-BX12 by stage 14.
Df(3R)Dl-BX12 embryos show defects in tracheal cell migration.
The Df(3R)Dl-BX12 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).
Shows dominant enhancement of dominant haltere phenotype caused by Ubx195 and Ubx9.22.
Heterozygous adults have significantly smaller phase delays than normal siblings in response to a 10 second pulse of blue light. Phase delays for heterozygotes are progressively larger in response to longer light pulses, but are not significantly different from control siblings.
The number of terminal tracheal branches (GB, LG and LH) are reduced by 30%-50% in heterozygous Df(3R)Dl-BX12 larvae.
No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.
Shows no maternal enhancement of dpphr4.
Heterozygotes with SerBd-3 are viable and exhibit a severe wing phenotype.
Deficient embryos show an uninterpretable mutant midgut phenotype.
Homozygous embryos are very abnormal compared to wild-type. Midgut primordia do not fuse and Malpighian tubules do not elongate normally.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
hide Stocks ( 2 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
Muskavitch.
 
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hide Synonyms & Secondary IDs ( 13 )
Reported As
Symbol Synonym
Df(3)Dl Bx12
Df(3R)DI-BX12
Df(3R)DLBX12
Df(3R) Dl-BX12
Name Synonym
Deficiency (3R) Delta
 
Secondary FlyBase IDs
hide References ( 55 )
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hide Recent research papers ( 1 )
Pueyo and Couso, 2011, Dev. Biol. 355(2): 183--193
Tarsal-less peptides control Notch signalling through the Shavenbaby transcription factor. [FBrf0213970]