FB2025_01 , released February 20, 2025
Aberration: Dmel\Df(3R)MAP11
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General Information
Symbol
Df(3R)MAP11
Species
D. melanogaster
Name
FlyBase ID
FBab0002606
Feature type
Computed Breakpoints include
Sequence coordinates
3R:6,667,543..6,675,282 [-] (Df(3R)MAP11:bk1)
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to wild type)
Class of aberration (relative to progenitor)
Breakpoints

84A1--2;84B1--2 [];[]

Carries alleles
Transposon Insertions
Formalized genetic data

bk1 hits lab << Dfd << bk2 << Scr

Genetic mapping information
Comments

Breakpoint 1 was mapped to an EcoRI-EcoRI restriction fragment. The position of the restriction fragment on the reference sequence was inferred by a FlyBase curator.

Comments on Cytology

Df(3R)MAP11 is broken in 84A1-84A2 and is a deletion of 84A4-84A5 (Ref: FBrf0048128). This ref should have said FBrf0070457 (Kaufman pers. comm.)

Left limit of break 1 from polytene analysis (FBrf0049494) Right limit of break 1 from inclusion of lab (FBrf0049494) Left limit of break 2 from polytene analysis (FBrf0049494) Right limit of break 2 from non-inclusion of Antp (FBrf0049494)

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 (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.
    In these cases, there will be no "Export to Hitlist" button to the left.
    Phenotypic Data
    In combination with other aberrations
    NOT in combination with other aberrations

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

    Heterozygosity for this deletion has no effect on 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 (3)
    Reported As
    Symbol Synonym
    Name Synonyms
    Secondary FlyBase IDs
      References (13)