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General Information
Symbol
Df(3R)BSC42
Species
D. melanogaster
Name
FlyBase ID
FBab0037759
Feature type
Computed Breakpoints include
Deleted Segment
Sequence coordinates
Member of large scale dataset(s)
Dfs_BSC_set1

A set of ~50 targeted deficiencies created by exploiting hybrid element insertion (HEI) and resolution; designed to fill gaps in deletion coverage.

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

The proximal breakpoint of Df(3R)BSC42 lies within the 98B1,2 doublet, leaving a portion of the doublet intact in the deletion chromosome.

Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
Partially deleted / disrupted
Molecular Data
Completely deleted
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)BSC42 mutant embryos display bifurcation defects of the abdominal segmental nerve (SNa) in which the dorsal, lateral, or both branches are missing with nearly the same penetrances.

The distal half of the salivary gland turns but the proximal half does not in embryos homozygous for Df(3R)BSC42 by stage 14.

Stocks (2)
Notes on Origin
Discoverer
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 

The miniwhite marker from P{EP}EP3088 was deleted or disrupted.

Synonyms and Secondary IDs (1)
References (13)