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General Information
Symbol
Df(3R)Exel6160
Species
D. melanogaster
Name
FlyBase ID
FBab0038215
Feature type
Computed Breakpoints include

[86E2-86E2];[86E11-86E11];

Deleted Segment
Sequence coordinates
3R:11,353,263..11,353,263 (Df(3R)Exel6160:bk1)
3R:11,569,189..11,569,189 (Df(3R)Exel6160:bk2)
Member of large scale dataset(s)
Dfs_Exelixis_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 set of 519 isogenic deletions provides 56% genome coverage.

The current Exelixis collection at the Bloomington Stock Center differs from the original described in FBrf0175003 : a significant number were shown not to carry a deletion and have been removed from the collection; a number of stocks have been lost; a number of additional deletions are included that were generated after publication.

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

Breakpoint based on release 3 sequence coordinate from Parks et al., 2004 (FBrf0174230), converted to release 5 coordinate.

Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.

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

Comments on Cytology
Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
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

The microtubule and centrosomal abnormalities (irregular number of centrosomes and spindle defects, including loss of astral microtubules) observed in brain neuroblasts in Pfdn2Δ10 single mutant and mgrG5308/Df(3R)Exel6160 third instar larvae are exacerbated further in Pfdn2Δ10,mgrG5308 double mutants.

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

Stocks (1)
Notes on Origin
Discoverer
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (8)