FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Aberration: Dmel\Df(1)RK5
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General Information
Symbol
Df(1)RK5
Species
D. melanogaster
Name
FlyBase ID
FBab0000677
Feature type
chromosomal_deletion
Computed Breakpoints include

12E9-12E11;13A9-13B1

Features within 12E9--13B1
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
In(1)366.2
(Drysdale et al., 1991)
In(1)N282.2
(Drysdale et al., 1991)
Mutagen
recombination
(Drysdale et al., 1991)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Harris et al., 1996, Mitchell et al., 1996, Pauli et al., 1995)
Breakpoints

12E9-12E11;13A9-13B1

(Harris et al., 1996, Pauli et al., 1995)

12E9-12E11;13B2-13B5

(Mitchell et al., 1996)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

mud << bk1 << NetA << eag << bk2

Genetic mapping information
Comments
Comments on Cytology

1B;12A6-12A10;13A2-13A5;20

(Drysdale et al., 1991)

All limits from polytene analysis (FBrf0080317)

Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
Adcy1
(Mitchell et al., 1996)
eag
(Drysdale et al., 1991)
NetA
(Harris et al., 1996, Mitchell et al., 1996)
NetB
(Harris et al., 1996, Mitchell et al., 1996)
Partially deleted / disrupted
Molecular Data
Completely deleted
Partially deleted
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

    Embryos exhibit variable defects in the formation of commissural pathways. Scer\GAL4rho.PL induced expression of P{UAS-NETA} or P{UAS-NETB} significantly rescued the CNS phenotype.

    (Harris et al., 1996)

    CNS defect in embryos: axon commissures are drastically thinner or missing amd the longitudinal tracts are highly disorganised and discontinuous.

    (Mitchell et al., 1996)

    Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.

    (Pauli et al., 1995)
    Stocks (0)
    Notes on Origin
    Discoverer

    W.R. Engels.

     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (2)
    Reported As
    Symbol Synonym
    Df(1)RK5
    In(1)N282.2L366.2R
    Name Synonyms
    Secondary FlyBase IDs
      References (14)