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General Information
Symbol
Df(2L)noc11
Species
D. melanogaster
Name
Deficiency (2L) no-ocelli
FlyBase ID
FBab0001857
Feature type
Computed Breakpoints include
[34E4--34F1];[35C3]
Deleted Segment
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to wild type)
Class of aberration (relative to progenitor)
Breakpoints
Carries alleles
Transposon Insertions
Formalized genetic data
bk1 hits rk << gft << bk2 << esg
Genetic mapping information
Comments
Comments on Cytology
Proximal breakpoint breaks within rk.
Left limit of break 1 from non-inclusion of rk (FBrf0084572) Right limit of break 1 from inclusion of rk (FBrf0084572) Left limit of break 2 from inclusion of gft (FBrf0051973) Right limit of break 2 from non-inclusion of esg (FBrf0051973)
Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Genes NOT Deleted / Disrupted
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 Df(2L)noc11 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).
Stocks (2)
Notes on Origin
Discoverer
Harrington.
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Breakpoints uncertain.
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
Name Synonyms
Deficiency (2L) no-ocelli
Secondary FlyBase IDs
    References (11)