A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(3L)fz-M21

General Information
SymbolDmel\Df(3L)fz-M21SpeciesD. melanogaster
NameFlyBase IDFBab0002373
Feature typechromosomal_deletion
Also Known AsDf(3L)fzM21, Df(3L)fzM21
Computed Breakpoints include 70D2;71E4-71E5
Deleted segment70D2--71E5
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
70D2-70D3;70E4-70E5
70D2;71E
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data btl << bk1 << fz << gnu << bk2
Genetic mapping information
Comments
hide Comments on Cytology
Limits of break 1 from polytene analysis (FBrf0075380) Limits of break 2 from polytene analysis (FBrf0076124)
 
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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
hide Related Comments
Does not delete P{lacW}endosS067006
hide Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations
Df(3L)fz-M21 embryos show defects in tracheal cell migration.
The Df(3L)fz-M21 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.
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.
Deficient embryos show an uninterpretable mutant midgut phenotype.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Trl hemizygous adult males show strong homeotic transformation of the sixth sternite into the fifth as shown by the presence of a bristles on the sixth sternite.
hide Stocks ( 5 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
Adler.
 
hide Balancer / Genotype Variants of the Aberration
hide Separable Components
hide Other Comments
Used in D.melanogaster/D.simulans hybrids to map at least four non-overlapping regions on the D.simulans 3R that have effects on the species difference of cuticular hydrocarbon profile.
"70D2;71E" was stated as revision.
hide Synonyms & Secondary IDs ( 7 )
Reported As
Symbol Synonym
Df(3L)fz-M21
Df(3L) fz-M21
Name Synonym
Secondary FlyBase IDs
hide References ( 50 )
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All research papers listed in FlyBase were published before 2011