FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Aberration: Dmel\Df(2L)ED3
Open Close
General Information
Symbol
Df(2L)ED3
Species
D. melanogaster
Name
FlyBase ID
FBab0029708
Feature type
chromosomal_deletion
Computed Breakpoints include

[35B2-35B2];[35D1-35D1];

Features within 35B2--35D1
Genomic Maps
Sequence coordinates
2L:14,490,575..14,490,575 (Df(2L)ED3:bk1)
(DrosDel Project, 2007.6.25)
2L:15,333,760..15,333,760 (Df(2L)ED3:bk2)
(DrosDel Project, 2007.6.25)
Member of large scale dataset(s)
Dfs_DrosDel_set1

A set of isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Initial core set of 209 isogenic deletions provides ~60% euchromatic genome coverage.

(Ryder et al., 2007)
Nature of Aberration
Cytological Order
Progenitor
P{RS5r}5-HA-1150
(Ryder et al., 2004, Ryder, 2003.6.17, Roote, 2002.2.6)
P{RS3r}CB-0183-3
(Ryder et al., 2004, Ryder, 2003.6.17, Roote, 2002.2.6)
Mutagen
FLPase
(Ryder et al., 2004, Ryder, 2003.6.17, Roote, 2002.2.6)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Ryder et al., 2004, Ryder, 2003.6.17, Roote, 2002.2.6)
Breakpoints

35B2;35D1

(FlyBase Curators, 2008)
Causes alleles
Carries alleles
Transposon Insertions
P{3'.RS5+3.3'}ED3
(Ryder et al., 2004, Ryder, 2003.6.17, Roote, 2002.2.6)
Formalized genetic data
Genetic mapping information
Comments
Comments on Cytology

Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.

(Ryder and Roote, 2005.11.4)

Confirmed by PCR (using the 3-step process described on http://www.drosdel.org.uk/del_confirm.php).

(Ryder and Roote, 2004.11.10)

Breakpoints predicted from derivation of chromosome have been confirmed by PCR.

(Roote, 2002.9.18)

Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}elBEP2039&P{PZ}osprJ571 and P{lacW}Su(H)k07904 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}esgEP633&P{PZ}esg07082 and P{lacW}CycEk05007&P{lacW}CycEk02602

Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Genes NOT Deleted / Disrupted
Genes Duplicated
Complementation Data
Completely duplicated
Partially duplicated
Molecular Data
Completely duplicated
Partially duplicated
Genes NOT Duplicated
Complementation Data
 
Molecular Data
 
Affected Genes Inferred by Location (108)
Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations
Stocks (3)
Notes on Origin
Discoverer
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (3)
References (23)