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General Information
Symbol
In(3R)ryps11136
Species
D. melanogaster
Name
FlyBase ID
FBab0005798
Feature type
Also Known As
ryps11136
Computed Breakpoints include

81F-h58;87D11

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

bk2 hits l(3)87Df

Genetic mapping information
Comments

Breakpoint(s) molecularly mapped

Right breakpoint at about 175 kb to the left of the origin of walk in the ry region; this origin is an arbitrary point which is in turn 6.5 kb to the right of the left breakpoint of In(3R)Cbxrv1.

Comments on Cytology

Breakpoint molecularly mapped.

Left limit of break 1 from polytene analysis (citation unavailable) Right limit of break 1 from polytene analysis (FBrf0040960) Limits of break 2 from complementation mapping against l(3)87Df (FBrf0040960)

Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
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
 
Affected Genes Inferred by Location
    Phenotypic Data
    In combination with other aberrations

    The position effect variegation of ry seen in In(3R)ryps11136 is suppressed in combination with Df(3R)l26c or Df(3R)l26d.

    No suppression of the ry position effect variegation phenotype is seen with either Df(2L)TW84 or 0.2M butyrate.

    NOT in combination with other aberrations

    Shows position-effect variegation for ry with respect to xanthine dehydrogenase activity in Malpighian tubules.

    homozygous lethal lethal when heterozygous with certain ry deficiencies. Purine sensitive when heterozygous with noncomplementing ry alleles.

    Stocks (0)
    Notes on Origin
    Discoverer
     

    Induced on a ry+11 chromosome.

    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    Analysis of the ry variegating phenotype associated with In(3R)ryps11136 suggests that position effect variegation may be due to a defect in transcription and is not due to underreplication of the position-affected gene (ry in this case).

    Synonyms and Secondary IDs (3)
    Reported As
    Symbol Synonym
    In(3R)ry-ps11136
    In(3R)ryps11136
    Name Synonyms
    Secondary FlyBase IDs
    • FBal0028537
    References (8)