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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]

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
 
Affected Genes Inferred by Location
    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)