Open Close
General Information
Symbol
Df(3R)crb-F89-4
Species
D. melanogaster
Name
FlyBase ID
FBab0002747
Feature type
Also Known As
Df(3R)F89-4, Df(3R)crbF89-4, Df(3R)crb89-4, Df(3R)crbF89-4
Computed Breakpoints include
95D7-95D11;95F15
Deleted Segment
Sequence coordinates
Member of large scale dataset(s)
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
bk1 << Mpk2B << bk2
Genetic mapping information
Comments
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Comments on Cytology
Ref: Tepass and Knust, 1990, Roux Arch. dev. Biol. 199(4): 189--206
All limits from polytene analysis (FBrf0091165)
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
Df(3R)jar322 is lethal in combination with Df(3R)crb-F89-4.
The position effect variegation of w seen in In(1)wm4 is suppressed by one copy of Df(3R)crb-F89-4.
NOT in combination with other aberrations
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
The Df(3R)crb-F89-4 chromosome does not act as a dominant suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion).
Heterozygosity for Df(3R)crb-F89-4 results in 1.9% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Suppresses the ommatidial polarity phenotype of dshhs.sev.B. Suppresses the ommatidial polarity phenotype of msnEP549 when driven by Scer\GAL4hs.2sev.
Stocks (2)
Notes on Origin
Discoverer
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (11)
References (41)