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General Information
D. melanogaster
FlyBase ID
Feature type
Also Known As
Computed Breakpoints include
Deleted Segment
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Class of aberration (relative to wild type)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data
wb << bk1 << l(2)34Fc << sna << bk2 << lace
Genetic mapping information
Comments on Cytology
Left limit of break 1 from non-inclusion of wb (citation unavailable) Right limit of break 1 from inclusion of l(2)34Fc (FBrf0092813) Left limit of break 2 from polytene analysis (FBrf0038047) Right limit of break 2 from polytene analysis (FBrf0036112)
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
Male sterile in combination with Df(2L)b78j. Male fertile in combination with Df(2L)b85f1 or Df(2L)b79b4.
NOT in combination with other aberrations
The Df(2L)do1 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).
Embryos have severe neural defects.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Stocks (2)
Notes on Origin
Balancer / Genotype Variants of the Aberration
Separable Components
Other Comments
Synonyms and Secondary IDs (3)
References (19)