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General Information
D. melanogaster
FlyBase ID
Feature type
Computed Breakpoints include


Sequence coordinates
3L:11,096,989..11,096,989 (Df(3L)ED4470:bk1)
3L:11,833,230..11,833,230 (Df(3L)ED4470:bk2)
Member of large scale dataset(s)

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.

Nature of Aberration
Cytological Order
Class of aberration (relative to wild type)
Class of aberration (relative to progenitor)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data
Genetic mapping information

This deletion removes multiple ribosomal protein-coding genes (in addition to other genes).

Comments on Cytology

Confirmed by 3-step PCR confirmation as shown in Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.

Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}l(3)0123901239&P{lacW}l(3)01239j9B4 and P{PZ}CycA02461&P{PZ}CycA03946 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}CycA02461&P{PZ}CycA03946 and P{PZ}rols08232&P{lacW}l(3)j2D3j2D3

Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
Partially deleted / disrupted
Molecular Data
Partially deleted
Genes NOT Deleted / Disrupted
Complementation Data
Molecular Data
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
Phenotypic Data
In combination with other aberrations

Inferred to overlap with: Df(3L)BSC379.

NOT in combination with other aberrations

No cardiac or bristle phenotypes are observed in heterozygous Df(3L)ED4470 mutant females.

Homozygous stage 16 embryos have elongated and convoluted tracheal dorsal trunks. The embryos also show defects in paracellular diffusion barrier function.

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

Stocks (2)
Notes on Origin
Balancer / Genotype Variants of the Aberration
Separable Components
Other Comments
Synonyms and Secondary IDs (5)
References (28)