FB2025_01 , released February 20, 2025
Aberration: Dmel\C(1;YL)wmMc
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General Information
Symbol
C(1;YL)wmMc
Species
D. melanogaster
Name
FlyBase ID
FBab0029163
Also Known As
In(1)wmMc
Computed Breakpoints include
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Mutagen
Class of aberration (relative to wild type)
Class of aberration (relative to progenitor)
Breakpoints
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data
Genetic mapping information
Comments
Comments on Cytology

X.YL translocation with the point of exchange in the rDNA.

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 (0)
    If no genes are listed here, it may be because the affected region is very large. The JBrowse insert above may show an error for the same reason, and other FlyBase tools such as CytoSearch may also fail for large regions. You can contact FlyBase for more help.
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    Phenotypic Data
    In combination with other aberrations

    C(1;YL)wmMc/0 ; T(Y;3)A78/+ males are fertile. Suppresses the In(2R)bwVDe2 pigmentation phenotype.

    The position effect variegation of Sb caused by T(2;3)SbV is strongly suppressed by C(1;YL)wmMc in both males and females. This interaction is both dominant and dosage sensitive; one copy of the C(1;YL)wmMc chromosome is sufficient to suppress variegation of Sb caused by T(2;3)SbV, however, two copies of C(1;YL)wmMc produce slightly greater suppression than one copy. The T(2;3)SbV chromosome may have a slight suppressing effect on the variegation of w caused by C(1;YL)wmMc in males. In(2R)bwVDe2 and C(1;YL)wmMc in combination show dominant suppression of variegation of one or both of w and bw, as measured by eye pigment levels.

    NOT in combination with other aberrations

    Eyes have a "peppered" phenotype - flecks of dark brown pigmented ommatidia are scattered throughout the wild type surface of the eye.

    Stocks (0)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    The chromosome referred to as "In(1)wmMc" in this paper is actually C(1;YL)wmMc (this chromosome is a descendent of In(1)wmMc which carries an X.YL translocation - see FBrf0123212 and Talbert and Henikoff, 2000.1.29, personal communication).

    The chromosome referred to as "white<up>mottled McLean</up>" in this paper is actually C(1;YL)wmMc (this chromosome is a descendent of In(1)wmMc which carries an X.YL translocation - see FBrf0123212 and Talbert and Henikoff, 2000.1.29, personal communication).

    The chromosome referred to as "wmMc" in this paper is actually C(1;YL)wmMc (this chromosome is a descendent of In(1)wmMc which carries an X.YL translocation - see FBrf0123212 and Talbert and Henikoff, 2000.1.29, personal communication).

    Synonyms and Secondary IDs (5)
    Reported As
    Name Synonyms
    white<up>mottled McLean</up>
    Secondary FlyBase IDs
      References (9)