FB2026_02 , released June 18, 2026
Insertion: Dmel\P{XP}d07693
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General Information
Symbol
Dmel\P{XP}d07693
Species
D. melanogaster
Name
FlyBase ID
FBti0069817
Feature type
transposable_element_insertion_site
Description
Inserted Element
P{XP}
LINE ID

d07693

Affected gene(s)
Viability / fertility
Associated allele(s)
Stock availability
None publicly available
Genomic Location
Chromosomal Location
3L ( 67B1 )
Sequence Location
3L:9,349,509..9,349,509 [+]
Target / Docking site
Genomic Maps
Member of Large Scale Dataset(s)
Dataset
TI_set_P{XP}.Exel.d
Description

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.

(Bellen et al., 2011)

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.

(Thibault et al., 2004)
Detailed Mapping Data
Chromosome (arm)

3L

(Andrade and Cook, 2005.7.22)
Sequence Location
3L:9,349,509..9,349,509 [+]
(FlyBase, 2005)
Orientation
Cytological location (computed by FlyBase)
67B1 (inferred by FlyBase from sequence location)
Cytological location (reported)
67A8 (reported as inferred from sequence location)
(Andrade and Cook, 2005.7.22, Gene Disruption Project members, 2001-)
Insertion into Natural transposon
Comments concerning location
Sequence Data
Inserted Element
Construct
P{XP}
Size (Kb)

7.303

Component Allele(s)
w+mC
Molecular map
Affected Gene(s)
Insertion may affect gene
Variant Molecular Consequences
Phenotypic Data
Associated Allele
Phenotypic Data
Expression Data
Reporter Expression
Additional Information
Statement
Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Data on Genetic Line
Line ID

d07693

(Gene Disruption Project members, 2001-)
Origin as a multiple insertion line
Progenitor(s) within the Genome
Related Aberration or Balancer
Aberration
Balancer
Stocks (0)
External Crossreferences and Linkouts ( 0 )
Comments
Comments

Exelixis, Inc. determined the insertion site of P{XP}d07693 to be at Release 3 genomic coordinate 9308161 on chromosome arm 3L.The Gene Disruption Project determined the insertion site of P{XP}d07693 to be at Release 3 genomic coordinate 9308219 on arm 3L.

(Andrade and Cook, 2005.7.22)

Location 3L:9323456-9323457 confirmed by FlyBase alignment of dbGSS accession CZ475874 to D. melanogaster arm Release_4 and heterochromatin Release_3.2b. Insertion orientation confirmed.

(FlyBase, 2005)
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
P{XP}d07693
(Andrade and Cook, 2005.7.22, FlyBase, 2005, FlyBase, 1992-)
Name Synonyms
Secondary FlyBase IDs
    References (6)