FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Aberration: Dmel\Df(3L)iro-DFM1
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General Information
Symbol
Df(3L)iro-DFM1
Species
D. melanogaster
Name
FlyBase ID
FBab0024879
Feature type
Also Known As
iroDFM1, Df(3)iroDFM1, Df(3L)iroDFM1
Computed Breakpoints include
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Class of aberration (relative to wild type)
Class of aberration (relative to progenitor)
Breakpoints
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
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 Df(3L)iro-DFM1 (containing araDFM1 and removing caup) clone cause a series of phenotypes, adding progressively more 'ventral-type' tissue in the following order: dorsal eye overgrowth or ectopic dorsal eyes, overgrowth of ventral type of cuticle (ptilinum and rostral membrane) ectopic antennal pouches, antenna and maxillary palps. The extra head structures are produced autonomously, but the eyes can be composed of both mutant and wild-type ommatidia. The ectopic ventral structures, all grow from the orbital region of the head. The rest of the dorsal head is displaced by the over-grown tissue.

    Df(3L)iro-DFM1 and Df(3L)iro-DFM3 cell clones in the notum have indistinguishable phenotypes. Clones of cells homozygous for Df(3L)iro-DFM1 or Df(3L)iro-DFM3 in the notum induced during the first or second larval instar show malformations. Notum is transformed to wing hinge, with sclerites and tegula-like cuticle with characteristic sensory structures. Surrounding wild type cells are recruited into the ectopic structures. Ectopic axillary sclerites were always in mirror image disposition to the regular ones. Malformations in the more central region of the notum caused failure of fusion of the heminota. Clones in the third instar wing disc organize a fold around themselves, similar to the fold found between the notum and wing hinge parts of the regular wing disc.

    Deletion causes embryonic or larval lethality. Transheterozygotes with mirrB1-12 are semi-lethal with rare escapers. Escapers show outheld wings, lack of alulae and deletion of the posterior supraalar bristle and/or anterior postalar bristle.

    When homozygous, in wing clones, differentiation of L5 and the alula fail. Dorsal clones remove L5 dorsally, and ventral clones remove L5 ventrally. No other site in the wing showed a requirement for ara-caup. Notum cells lacking ara and caup are inviable.

    Stocks (1)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (5)
    Reported As
    Name Synonyms
    Secondary FlyBase IDs
      References (8)