A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Dmel\P{EP}CG13359G17050 Insertion

General Information
Symbol Dmel\P{EP}CG13359G17050 Species D. melanogaster
Name FlyBase ID FBti0131356
Feature type transposable_element_insertion_site
Description
Inserted element P{EP} Expression data
Affected gene(s) CG13359 Viability / fertility fertile, viable
Causes allele(s) CG13359G17050 Stock availability 1 publicly available
LINE ID G17050
Genomic Location
Chromosomal location X ( 1C5 ) Sequence location X:695,766..695,766 [-]
Map ( GBrowse ) GBrowse View Help detailed view FBti0028656 FBti0027298 FBti0028442 FBti0076911 FBti0054134 FBti0039421 FBti0071470 FBti0131356 FBti0042119 FBti0024111 FBti0059145 FBti0071950 FBti0038745
Member of Large Scale Dataset(s)
Dataset

A set of transgenic insertion stocks derived by TE mobilization using the using the P-element construct P{EP}. The P{EP} construct construct carries a w[+mC] mini-white visible marker, Scer\UAS binding sites for the Scer\GAL4 transcriptional regulator, and bacterial sequences that allow plasmid rescue (FBrf0090768). The GAL4-UAS system allows regulated expression of genes proximate to the site of the insertion: genes properly oriented with respect to the Scer\UAS sequences can be conditionally expressed via transgene-derived Scer\GAL4 activity.
(Bellen et al., 2011)
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Description
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FB2013_03
FB2013_02
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Chromosome (arm)
Sequence Location
X:695,766..695,766 [-]
(Bellen, 2010.10.18)
Orientation
Cytological location
(computed by FlyBase)
1C5 ( inferred by FlyBase from sequence location )
Cytological location
(reported)
1C5 (reported as inferred from sequence location)
(Bellen, 2010.10.18)
Comments concerning
location
hide Sequence Data
Flanking sequence
HN339244
(Bellen, 2010.10.18)
hide Inserted Element
Construct P{EP}
Location-dependent
role
mobile activating element (UASG)
(Rorth, 1996)
Size 7.987Kb
Associated alleles
Scer\UAS14x.hs
TrlBRcRa
w+mC
Molecular map
hide Affected Gene(s)
Insertion may
affect gene
CG13359
(Bellen, 2010.10.18)
hide Alleles and Phenotypes
Causes alleles
CG13359G17050
(Bellen, 2010.10.18)
Lethality
References
viable
(Bellen, 2010.10.18)
Sterility
References
fertile
(Bellen, 2010.10.18)
hide Phenotype Manifest In
hide Detailed Description
Statement
Reference
hide Expression Data
Reporter Expression
Additional Information
Statement
Reference
Marker for
Reflects
expression of
Reporter construct
used in assay
hide External Images
FlyView (LinkOut)
hide Data on Genetic Line
Line ID
G17050
(Bellen, 2010.10.18)
Origin as a multiple insertion line
N
(Bellen, 2010.10.18)
hide Progenitor(s) within the Genome
hide Related Aberration or Balancer
Aberration
Balancer
hide Stocks ( 1 )
Bloomington
32641
P{EP}CG13359G17050 w*
hide Linkouts
hide Synonyms & Secondary IDs
Reported As
Symbol Synonym
P{EP}CG13359G17050
(Bellen, 2010.10.18, )
Secondary FlyBase IDs
hide References ( 5 )
Research paper
Bellen et al., 2011, Genetics 188(3): 731--743
The Drosophila gene disruption project: progress using transposons with distinctive site specificities. [FBrf0214229]
Bellen et al., 2004, Genetics 167(2): 761--781
The BDGP gene disruption project: single transposon insertions associated with 40% of Drosophila genes. [FBrf0179132]
Rorth, 1996, Proc. Natl. Acad. Sci. U.S.A. 93(22): 12418--12422
A modular misexpression screen in Drosophila detecting tissue-specific phenotypes. [FBrf0090768]
Personal communication to FlyBase
Bellen, 2010.10.18, BDGP_2010_1022.GenExel.xml
BDGP_2010_1022.GenExel.xml [FBrf0212107]
FlyBase analysis
FlyBase Curators, 2013, Members of TE insertion collections.
Members of TE insertion collections. [FBrf0220668]