FB2025_01 , released February 20, 2025
Insertion: Dmel\P{lacW}IshaSH1128
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General Information
Symbol
Dmel\P{lacW}IshaSH1128
Species
D. melanogaster
Name
FlyBase ID
FBti0025980
Feature type
transposable_element_insertion_site
Description
Inserted Element
P{lacW}
LINE ID

SH1128

Affected gene(s)
Isha
Viability / fertility
viable
Associated allele(s)
IshaSH1128
Stock availability
1 publicly available
Genomic Location
Chromosomal Location
2R ( 57C7 )
Sequence Location
2R:21,168,208..21,168,208 [+]
Target / Docking site
Genomic Maps
Member of Large Scale Dataset(s)
Dataset
TI_set_P{lacW}.SH
Description

Insertion lines from this collection were assessed for inclusion in the Gene Disruption Project collection.

(Bellen et al., 2011)

A set of mutant stocks derived by insertional mutagenesis using the P-element construct P{lacW}; most lines have a lethal phenotype. The P{lacW} construct carries a w+mC mini-white visible marker, Ecol\lacZ enhancer trap sequences, and bacterial sequences that allow plasmid rescue (FBrf0049800).

(Oh et al., 2003)
Detailed Mapping Data
Chromosome (arm)
Sequence Location
2R:21,168,208..21,168,208 [+]
(Levis and Carlson, 2011.9.12)
Orientation

+

(Levis and Carlson, 2011.9.12)
Cytological location (computed by FlyBase)
57C7 (inferred by FlyBase from sequence location)
Cytological location (reported)
57C3-57C5 (reported as inferred from sequence location)
(Oh et al., 2003)
57C7_r5 (reported as inferred from sequence location)
(Levis and Carlson, 2011.9.12)
Insertion into Natural transposon
Comments concerning location

Genomic location previously reported as 2R:17055510..17055720 .

(FlyBase, 2005)
Sequence Data
Inserted Element
Construct
P{lacW}
Size (Kb)

10.691

Component Allele(s)
w+mC
Molecular map
Affected Gene(s)
Insertion may affect gene
Isha
(Kahsai et al., 2016, FlyBase Curators, 2008-, Oh et al., 2003)
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

SH1128

(Levis and Carlson, 2011.9.12)
Origin as a multiple insertion line
Progenitor(s) within the Genome
Related Aberration or Balancer
Aberration
Balancer
Stocks (1)
External Crossreferences and Linkouts ( 1 )
Crossreferences
GenBank Nucleotide - A collection of sequences from several sources, including GenBank, RefSeq, TPA, and PDB.
Comments
Comments

Deficiency complementation analysis indicates that the lethality of the chromosome is separable from the P{lacW}CG4266SH1128 insertion.

(Kahsai et al., 2016)

Location 2R:16675586-16675798 confirmed by FlyBase alignment of dbGSS accession AB082402 to D. melanogaster arm Release_4 and heterochromatin Release_3.2b. Insertion orientation confirmed.

(FlyBase, 2005)
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
P{lacW}CG4266SH1128
P{lacW}IshaSH1128
P{lacW}l(2)SH1128SH1128
(FlyBase, 2005, Oh et al., 2003, FlyBase, 1992-)
SH1128
(Levis and Carlson, 2011.9.12)
Name Synonyms
Secondary FlyBase IDs
    References (7)