A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Recombinant construct P{UAS-ECFP-ER}

General Information
Symbol P{UAS-ECFP-ER} FlyBase ID FBtp0021545
Feature type transgenic_transposon
Size Expression data
Associated insertions 0 available
Molecular map
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Description
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FB2013_03
FB2013_02
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hide Description & Uses
Species synthetic construct
Location-dependent
role
Description
CV term
Qualifiers & info
Reference
Uses
CV term
Qualifiers & info
Reference
Cloning Sites
Location
Restriction sites
Reference
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Sequence (FB)
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Extent
 
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Total Size
Left end
Right end
Segments
Number
Orientation
Symbol
Reference
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CV term
Qualifiers & info
Reference
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Allele Avic\GFPECFP.ER.Scer\UAS.T:Uuuu\KDEL
Reference(s) (Ishikawa et al., 2005, Sasamura et al., 2007, Yamakawa et al., 2012, Ishikawa et al., 2010)
Molecular data
Construct: Avic\GFP-ECFP, with an Endoplasmic Reticulum (ER)-retention signal (KDEL) is cloned downstream of Scer\UAS regulatory sequences.
Phenotypic class
Phenotype manifest in
Other information
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Reporter Expression
Additional Information
Statement
Reference
Marker for
Reflects expression of
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progenitor(s)
descendant(s)
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Other Crossreferences
Linkouts
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Reported As
Symbol Synonym
P{UAS-ECFP-ER}
 
Secondary FlyBase IDs
hide References ( 4 )
Research paper
Yamakawa et al., 2012, Development 139(3): 558--567
Deficient Notch signaling associated with neurogenic pecanex is compensated for by the unfolded protein response in Drosophila. [FBrf0217160]
Ishikawa et al., 2010, J. Biol. Chem. 285(6): 4122--4129
Two pathways for importing GDP-fucose into the endoplasmic reticulum lumen function redundantly in the O-fucosylation of Notch in Drosophila. [FBrf0209841]
Sasamura et al., 2007, Development 134(7): 1347--1356
The O-fucosyltransferase O-fut1 is an extracellular component that is essential for the constitutive endocytic trafficking of Notch in Drosophila. [FBrf0191989]
Ishikawa et al., 2005, Proc. Natl. Acad. Sci. U.S.A. 102(51): 18532--18537
Notch deficiency implicated in the pathogenesis of congenital disorder of glycosylation IIc. [FBrf0191442]