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General Information
Symbol
Df(3R)ED4688
Species
D. melanogaster
Name
FlyBase ID
FBab0047183
Feature type
Computed Breakpoints include
Sequence coordinates
3L:17,533,091..17,533,091 (Df(3R)ED4688:bk1)
3L:17,612,170..17,612,170 (Df(3R)ED4688:bk2)
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.
Nature of Aberration
Cytological Order
Progenitor
Class of aberration (relative to wild type)
Class of aberration (relative to progenitor)
Breakpoints
Causes alleles
Carries alleles
Formalized genetic data
Genetic mapping information
Comments
Scer\FRT-mediated recombination between the two progenitor insertions has resulted in the deletion of 79,079 bp of genomic sequence between them, including the entire Nedd4 open reading frame and four other genes.
Comments on Cytology
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
 
Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations
Homozygous Df(3R)ED4688 stage 16 embryos do not display any midline crossing defects.
Stocks (0)
Notes on Origin
Discoverer
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
Df(3R)ED4688
Name Synonyms
Secondary FlyBase IDs
    References (2)