FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Aberration: Dmel\Df(3L)eygC1
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General Information
Symbol
Df(3L)eygC1
Species
D. melanogaster
Name
FlyBase ID
FBab0028386
Feature type
Also Known As
Df(3L)eygC1, Df(3L)eyg-C1
Computed Breakpoints include

69A4-69A5;69D4-69D6

Sequence coordinates
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

69A4-69A5;69D4-69D6

Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

bk1 << eyg << bk2

Genetic mapping information
Comments
Comments on Cytology

All limits from polytene analysis (FBrf0104918)

Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
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

    The Df(3L)eygC1 chromosome does not act as a dominant suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion).

    The number of finger-like sensillae of the antennal organ is reduced in homozygous embryos and the sensillae only rarely reach full length. The salivary duct primordium forms normally in homozygous embryos but is unable to complete the first convergence and extension and instead remains as two clumps of cells. Later, the duct cells move anteriorly in a process resembling wild-type, although they do not obviously converge towards the ventral midline. Approximately 75% of embryos have no individual salivary ducts, and the remaining 25% have only one individual salivary duct which is almost always malformed. A common salivary duct sometimes forms in these embryos, sometimes appearing broader than wild-type. Homozygotes die as embryos.

    Stocks (2)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (6)
    References (14)