FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Insertion: Dmel\P{EP}CG14408G982
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General Information
Symbol
Dmel\P{EP}CG14408G982
Species
D. melanogaster
Name
FlyBase ID
FBti0169336
Feature type
transposable_element_insertion_site
Description
Inserted Element
P{EP}
LINE ID

G982

Affected gene(s)
CG14408
Viability / fertility
fertile, viable
Associated allele(s)
CG14408G982
Stock availability
2 publicly available
Genomic Location
Chromosomal Location
X ( 12F5 )
Sequence Location
X:14,827,912..14,827,912 [+]
Target / Docking site
Genomic Maps
Member of Large Scale Dataset(s)
Dataset
TI_set_P{EP}.G
Description

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)
Detailed Mapping Data
Chromosome (arm)
Sequence Location
X:14,827,912..14,827,912 [+]
(Bellen, 2015.7.10)
Orientation
Cytological location (computed by FlyBase)
12F5 (inferred by FlyBase from sequence location)
Cytological location (reported)
12F5 (reported as inferred from sequence location)
(Bellen, 2015.7.10)
Insertion into Natural transposon
Comments concerning location
Sequence Data
Flanking sequence
KS307062
(Bellen, 2015.7.10)
Inserted Element
Construct
P{EP}
(Bellen, 2015.7.10)
Size (Kb)

7.987

Component Allele(s)
w+mC
Molecular map
Affected Gene(s)
Insertion may affect gene
CG14408
(Korea Drosophila Resource Center, 2022.2.11, Bellen, 2015.7.10)
Variant Molecular Consequences
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

G982

(Bellen, 2015.7.10)
Origin as a multiple insertion line

P

(Bellen, 2015.7.10)
Progenitor(s) within the Genome
Related Aberration or Balancer
Aberration
Balancer
Stocks (2)
External Crossreferences and Linkouts ( 0 )
Comments
Comments

LINECOMMENT:Flanks map 1.8 kb apart, consistent with 2 insertions or 1 insertion associated with a rearrangement. The last few nucleotides of the 5prime end of the P element are missing, suggesting a deletion

(Bellen, 2015.7.10)
Synonyms and Secondary IDs (4)
References (3)