FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
Aberration: Dmel\Df(2R)ED2098
Open Close
General Information
Symbol
Df(2R)ED2098
Species
D. melanogaster
Name
FlyBase ID
FBab0033393
Feature type
chromosomal_deletion
Computed Breakpoints include

[47A7-47A7];[47C6-47C6];

Features within 47A7--47C6
Genomic Maps
Sequence coordinates
2R:10,416,861..10,416,861 (Df(2R)ED2098:bk1)
(DrosDel Project, 2007.6.25)
2R:10,899,206..10,899,206 (Df(2R)ED2098: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{RS3r}CB-0306-3
(Ryder and Roote, 2005.11.4)
P{RS5r}5-SZ-3992
(Ryder and Roote, 2005.11.4)
Mutagen
FLPase
(Ryder and Roote, 2005.11.4)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Ryder and Roote, 2005.11.4, Ryder, 2003.6.17)
Breakpoints

47A7;47C6

(FlyBase Curators, 2008)
Causes alleles
Carries alleles
Transposon Insertions
P{3'.RS5+3.3'}ED2098
(Ryder and Roote, 2005.11.4)
Formalized genetic data
Genetic mapping information
Comments
Comments on Cytology

Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.

(Ryder and Roote, 2005.11.4)

Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}Hr46k10308 and P{PZ}lola00349&P{EP}lolaEP952 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k15826k15826&P{EP}EP471 and P{EP}shnEP2359&P{EP}shnEP644

Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
l(2)47A7
(Otte et al., 2009)
l(2)47A9-5
(Otte et al., 2009)
l(2)47A9-6
(Otte et al., 2009)
lola
(Kahsai et al., 2016, Otte et al., 2009)
stan
(Kahsai et al., 2016)
Partially deleted / disrupted
Molecular Data
Completely deleted
RpS15Ab
(Marygold et al., 2007)
Partially deleted
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 (72)
Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations

No cardiac or bristle phenotypes are observed in heterozygous Df(2R)ED2098 mutant females.

(Casad et al., 2011)

Flies heterozygous for the deletion do not show a Minute bristle phenotype.

(Marygold et al., 2007)
Stocks (2)
Notes on Origin
Discoverer
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Df(2R)ED2098
(Hope et al., 2019, Lee et al., 2018, Kahsai et al., 2016, Tripathy et al., 2014, Casad et al., 2011, FlyBase Curators, 2008, Kucherenko et al., 2008)
Df(2R)ED2098
(Otte et al., 2009)
Name Synonyms
Secondary FlyBase IDs
    References (14)