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General Information
Symbol
Df(3R)96B
Species
D. melanogaster
Name
FlyBase ID
FBab0014464
Feature type
Computed Breakpoints include
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to wild type)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

tok << bk1 << l(3)96Bg << l(3)96Ba << bk2

Genetic mapping information
Comments
Comments on Cytology

Molecular mapping indicates that one breakpoint of this deficiency is between tok and tld and the other is between CG31120 and CG13646.

All limits from polytene analysis (Nairz, 2002.6.28, pc)

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

    Heterozygosity for Df(3R)96B results in 2.7% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.

    Homozygous embryos have normal gut morphology.

    Stocks (2)
    Notes on Origin
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    Using a local high-density SNP map the borders of Df(3R)96B have been placed between tok and tld on the proximal side and between CG31120 and CG13646 on the distal side. As ssh (96B10/B11) is complemented by the deficiency, the distal breakpoint must be situated somewhere between CG31120 (at 96B8) and Osbp (96B10).

    Synonyms and Secondary IDs (2)
    Reported As
    Symbol Synonym
    Name Synonyms
    Secondary FlyBase IDs
      References (13)