FB2026_03 , released September 17, 2026
Aberration: Dmel\In(3LR)TM6C
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General Information
Symbol
In(3LR)TM6C
Species
D. melanogaster
Name
FlyBase ID
FBab0005466
Feature type
Computed Cytological Breakpoints (relative to progenitor)
Sequenced Breakpoints (relative to progenitor)
Member of large scale dataset(s)
Nature of Aberration
Cytological Order

3Lt - 61A1 | 87B2 - 75C | 94A - 100F2 | 92D1 - 87B4 | 61A2 - 63B8 | 72E1 - 63B9 | 72E2 - 75C | 94A - 92D9 | 100F3 - 3Rt

Mutagen
Class of aberration (relative to wild type)
Class of aberration (relative to progenitor)
Cytological Breakpoints (relative to progenitor)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data
Genetic mapping information
Comments
Comments on Cytology
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
    NOT in combination with other aberrations

    Homozygous viable, although homozygotes show lower viability and longer development time than wild type.

    Stocks (0)
    Notes on Origin
    Discoverer

    Craymer, 1982.

     

    Generated by recombining TM6 with a chromosome carrying In(3LR)HR33 (61A1-2;87B). The recombination resulted in the replacement of the left end of In(3LR)P88 with the left end of In(3LR)HR33. The right breakpoint of In(3LR)P88 (order 89C4|61A2) was then replaced with the right breakpoint of In(3LR)HR33 (order 87B4|61A2) by double crossover (FBrf0063387). An unknown female sterile mutation was present near the distal end of In(3R)C in the progenitor TM6 chromosome in region 92F, but it was probably removed by recombination with a In(3R)C lacking this mutation during the construction of TM6C since this balancer was originally homozygous viable and fertile.

    Balancer / Genotype Variants of the Aberration
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (3)
    Reported As
    Symbol Synonym
    In(3LR)TM6C
    Name Synonyms
    Third Multiple Six, C structure
    Secondary FlyBase IDs
      References (9)