FB2026_03 , released September 17, 2026
Aberration: Dmel\Df(1)v-N48
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General Information
Symbol
Df(1)v-N48
Species
D. melanogaster
Name
FlyBase ID
FBab0009094
Feature type
chromosomal_deletion
Also Known As
Df(1)vN48
Computed Cytological Breakpoints (relative to progenitor)
Features within 9F--10C5
Sequenced Breakpoints (relative to progenitor)
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Tp(1;1)vN48
Mutagen
recombination
Class of aberration (relative to wild type)
chromosomal_deletion
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
DDBJ / EMBL / GenBank
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

    Homozygous embryos have normal gut morphology.

    (Merabet et al., 2002)

    Intermediate second site non-complementing phenotype with zipEbr and zipmhc-c6.1 : malformed phenotype penetrance 25-75%.

    (Halsell and Kiehart, 1998)

    Deficient embryos show an uninterpretable mutant midgut phenotype.

    (Bilder and Scott, 1995)

    Homozygous embryos are very abnormal compared to wild-type and cease development at a number of different stages.

    (Harbecke and Lengyel, 1995)

    fz24 homozygotes exhibit a weak multiple hair cell (MHC) phenotype that can be enhanced by a decrease in dsh+ gene dosage. The early phenotype of P{hsfzI} can be suppressed by a decrease in dsh+ gene dosage.

    (Krasnow et al., 1995)
    Stocks (2)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (2)
    Reported As
    Symbol Synonym
    Df(1)v-N48
    (Li et al., 2021, Satoh et al., 2008)
    Df(1)vN48
    (Brumby et al., 2004, Lammel and Saumweber, 2000, Zhang et al., 1990, Voelker et al., 1985)
    Name Synonyms
    Secondary FlyBase IDs
      References (17)