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General Information
Symbol
Df(2L)pr76
Species
D. melanogaster
Name
Deficiency (2L) purple
FlyBase ID
FBab0001899
Feature type
Also Known As
Df(2L)pr76
Computed Breakpoints include

37D;38E5-38E10

Deleted Segment
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Class of aberration (relative to wild type)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

bk1 << spi << cad << bk2

Genetic mapping information
Comments
Comments on Cytology

Ref: Lindsley and Zimm, 1992

Limits of break 1 from polytene analysis (FBrf0034393) Left limit of break 2 from inclusion of cad (FBrf0082073) Right limit of break 2 from polytene analysis (FBrf0034393)

Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
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

Heterozygosity for Df(2L)pr76 results in 0.2% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.

Shows no maternal enhancement of dpphr4.

Dominantly causes tergite defects in less than 50% of run3 heterozygotes.

Deficient embryos show an uninterpretable mutant midgut phenotype.

Heterozygosity for this deletion suppresses the mutant ovarian phenotype of ovoD2.

Stocks (2)
Notes on Origin
Discoverer
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
Name Synonyms
Deficiency (2L) purple
Secondary FlyBase IDs
    References (18)