A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(3R)Tl-P

General Information
SymbolDmel\Df(3R)Tl-PSpeciesD. melanogaster
NameDeficiency (3R) TollFlyBase IDFBab0002666
Feature typechromosomal_deletion
Also Known AsDf(3R)T1-P, Df(3R)5BRXP, Df(3R)TI-P
Computed Breakpoints include 97A;98A1-98A2
Deleted segment97A--98A2
Map ( GBrowse ) GBrowse View Help Untitled Document detailed view
Sequence coordinates
3R:21,885,676..21,903,734 (Df(3R)Tl-P:bk1)
3R:23,214,330..23,305,922 (Df(3R)Tl-P: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
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data Indf << bk1 << spn-D << goul << bk2
Genetic mapping information
Comments
hide Comments on Cytology
The left Df(3R)Tl-P breakpoint lies within CG14551 or dys or in a region between these genes, and lies in the range 3R:21885676..21903734 (R5) (predicted cytology: 96F10-12).
The right Df(3R)Tl-P breakpoint probably lies within side, CG13978 or Cyp6a18 or in a region between these genes, and lies in the range 3R:23214330..23305922 (R5) (predicted cytology: 97F8-98A2).
Limits of break 1 from polytene analysis (FBrf0042050) Limits of break 2 from polytene analysis (FBrf0064394)
 
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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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hide Phenotypic Data
In combination with other aberrations
Inferred to overlap with: Df(3R)Espl3.
No effect on In(1)wm4h position-effect variegation.
NOT in combination with other aberrations
The Df(3R)Tl-P 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)Tl-P results in 3.7% X chromosome nondisjunction and 5.6% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Causes inviability or low viability 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.
Heterozygotes with Df(3R)Dl-BX6 are fully viable.
Wild type nonanol phenotype; repulsion.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Midgut development of mutant embryos is wild type.
Homozygous embryos have smaller heads than normal.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
heterozygous females viable heterozygous females fertile
 
hide Stocks ( 3 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
Anderson.
 
Revertant
 
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hide Synonyms & Secondary IDs ( 17 )
Reported As
Symbol Synonym
Df(3R)Tl-5BRXP
Df(3R)Tl5BRXP
 
Df(3R)Tl5BRXP
Df(3R)TL-P
Name Synonym
Deficiency (3R) Toll
 
Secondary FlyBase IDs
  • FBab0002477
  • FBab0027963
hide References ( 56 )
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hide Recent research papers ( 3 )
Miller et al., 2012, J. Neurogenet. 26(3-4): 317--327
A mutation in Drosophila Aldolase Causes Temperature-Sensitive Paralysis, Shortened Lifespan, and Neurodegeneration. [FBrf0220234]
Ghabrial et al., 2011, PLoS Genet. 7(7): e1002087
A systematic screen for tube morphogenesis and branching genes in the Drosophila tracheal system. [FBrf0214368]
McElwain et al., 2011, PLoS ONE 6(11): e26993
A suppressor/enhancer screen in Drosophila reveals a role for wnt-mediated lipid metabolism in primordial germ cell migration. [FBrf0216663]