A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(2L)E55

General Information
SymbolDmel\Df(2L)E55SpeciesD. melanogaster
NameFlyBase IDFBab0001458
Feature typechromosomal_deletion
Computed Breakpoints include 37D2;38A1
Deleted segment37D2--38A1
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Error

No matching regions found.

Sequence coordinates
2L:19,691,199..19,701,224 [+] (Df(2L)E55:bk2)
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
37C6-37D1;37F5-38A1
37D2-37E1;35F5-38A1
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data γTub37C << bk1 << l(2)37Da << fs(2)lto3 << bk2 << Lar
Genetic mapping information
Comments
Breakpoint(s) molecularly mapped
hide Comments on Cytology
Left limit of break 1 from polytene analysis (FBrf0028752) Right limit of break 1 from inclusion of l(2)37Da (citation unavailable) Left limit of break 2 from inclusion of Lar (FBrf0086508) Right limit of break 2 from polytene analysis (FBrf0028752)
 
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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
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
The width of the CNS is closer to wild-type in Df(2L)E55 ; Df(3L)H99 double mutant embryos than in Df(2L)E55 single mutant embryos, although commissure separation remains incomplete.
No effect on In(1)wm4h position-effect variegation.
Df(2L)E55/Df(2L)TW330 lethal Df(2L)E55/Df(2L)VA15 lethal Df(2L)E55/Df(2L)VA20 lethal Df(2L)E55/Df(2L)VA22 lethal Df(2L)E55/Df(2L)VA23 lethal Df(2L)E55/Df(2L)VA25 lethal Df(2L)E55/Df(2L)TW9 lethal Df(2L)E55/Df(2L)TW12 lethal Df(2L)E55/Df(2L)TW150 viable Df(2L)E55/Df(2L)TW84 viable Df(2L)E55/Df(2L)OD16 viable Df(2L)E55/Df(2L)TW150 non-transparent wing phenotype Df(2L)E55/Df(2L)TW84 non-transparent wing phenotype Df(2L)E55/Df(2L)OD16 non-transparent wing phenotype
 
NOT in combination with other aberrations
Heterozygosity for Df(2L)E55 results in 3.5% X chromosome nondisjunction and 2.4% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Shows no maternal enhancement of dpphr4.
The central nervous system (CNS) is narrower than normal and the commissures are thicker than normal and incompletely separated in Df(2L)E55 embryos.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Midgut development of mutant embryos is wild type.
Homozygous embryos do not always complete head involution.
Heterozygosity for this deletion suppresses the mutant ovarian phenotype of ovoD2.
hide Stocks ( 3 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
hide Balancer / Genotype Variants of the Aberration
hide Separable Components
hide Other Comments
The Df(2L)E55 chromosome acts as a dominant moderate 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), but this is a false positive result (the suppressor is not within the bounds of the deficient region) because the region of the deficiency is covered by one or more nonsuppressing deficiencies.
hide Synonyms & Secondary IDs ( 4 )
Reported As
Symbol Synonym
Df(2L)TWE55
Name Synonym
Secondary FlyBase IDs
hide References ( 44 )
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