A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Dmel\P{XP}Fucad02798 Insertion

General Information
Symbol Dmel\P{XP}Fucad02798 Species D. melanogaster
Name FlyBase ID FBti0042785
Feature type transposable_element_insertion_site
Description
Inserted element P{XP} Expression data
Affected gene(s) CG11714, Fuca Viability / fertility
Causes allele(s) CG11714d02798, Fucad02798 Stock availability 2 publicly available
LINE ID d02798
Genomic Location
Chromosomal location 3L ( 68C12 ) Sequence location 3L:11,514,389..11,514,389 [+]
Map ( GBrowse ) GBrowse View Help detailed view FBti0060698 FBti0041332 FBti0113110 FBti0109537 FBti0105331 FBti0054938 FBti0042785 FBti0046014 FBti0049682
Member of Large Scale Dataset(s)
Dataset

A set of transgenic insertion stocks derived by TE mobilization using the P-element construct P{XP}. The P{XP} construct carries the w[+mC] mini-white marker, long (199-bp) Scer\FRT sites, and is designed to allow flexible use of Scer\UAS sites for Scer\GAL4-driven misexpression of adjacent genes. FRT sites allow Scer\FLP-mediated recombination between other FRT-containing elements, and thus can be used to generate molecularly defined deletions.
P{XP} insertion lines from Exelixis were remapped and assessed for inclusion in the Gene Disruption Project collection; flanking sequence data were submitted to GenBank.
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Description
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FB2013_03
FB2013_02
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Chromosome (arm)
Sequence Location
3L:11,514,389..11,514,389 [+]
Orientation
Cytological location
(computed by FlyBase)
68C12 ( inferred by FlyBase from sequence location )
Cytological location
(reported)
68C12 (reported as inferred from sequence location)
Comments concerning
location
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Flanking sequence
hide Inserted Element
Construct P{XP}
Location-dependent
role
deletion generation component
mobile activating element
carries FRT site(s)
Size 7.303Kb
Associated alleles
Molecular map
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Insertion may
affect gene
hide Alleles and Phenotypes
Causes alleles
Lethality
References
Sterility
References
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Statement
Reference
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Reporter Expression
Additional Information
Statement
Reference
Marker for
Reflects
expression of
Reporter construct
used in assay
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FlyView (LinkOut)
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Line ID
Origin as a multiple insertion line
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Aberration
Balancer
hide Stocks ( 2 )
Bloomington
Harvard
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hide Comments
Location 3L:11495235-11495236 determined by FlyBase alignment of dbGSS accession CZ473002 to D. melanogaster arm Release_4 and heterochromatin Release_3.2b. Insertion orientation revised.
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Reported As
Symbol Synonym
P{XP}CG6128d02798
P{XP}CG33047d02798
P{XP}Fucad02798
 
Secondary FlyBase IDs
hide References ( 11 )
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]
Thibault et al., 2004, Nat. Genet. 36(3): 283--287
A complementary transposon tool kit for Drosophila melanogaster using P and piggyBac. [FBrf0175002]
Supplementary material
Thibault, 2004, Nature Genetics 36(3):
Supplementary Table 2. [FBrf0174227]
Thibault, 2004, Nature Genetics 36(3):
Supplementary Table 3. [FBrf0174228]
Personal communication to FlyBase
Bloomington Drosophila Stock Center, 2004.11.6, Exelixis insertion alleles that are not in FlyBase.
Exelixis insertion alleles that are not in FlyBase. [FBrf0179797]
Gene Disruption Project members, 2001-, (Computer file)
(Computer file) [FBrf0132177]
FlyBase analysis
FlyBase Curators, 2013, Members of Exelixis insertion collections: P{XP}, PBac{PB}, PBac{RB}, PBac{WH}.
Members of Exelixis insertion collections: P{XP}, PBac{PB}, PBac{RB}, PBac{WH}. [FBrf0221061]
FlyBase, 2005, Assessment of transgenic construct insertion sites.
Assessment of transgenic construct insertion sites. [FBrf0184339]
FlyBase, 1996-, FlyBase inference based on genome sequence analysis.
FlyBase inference based on genome sequence analysis. [FBrf0104946]
FlyBase, 1992-, FlyBase curation.
FlyBase curation. [FBrf0105495]