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General Information
Symbol
Df(1)HF368
Species
D. melanogaster
Name
FlyBase ID
FBab0000429
Feature type
Computed Breakpoints include
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Class of aberration (relative to wild type)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

cac << bk1 << l(1)11Ad << Lsp1α << bk2

Genetic mapping information
Comments

Breaks within protein coding region and deletes the 5' (proximal) portion of the gene.

Comments on Cytology

Deletion of 18/22 bands.

Left limit of break 1 from polytene analysis (FBrf0034402) Right limit of break 1 from inclusion of gd (FBrf0102954) Limits of break 2 from polytene analysis (FBrf0034402)

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
    Phenotypic Data
    In combination with other aberrations
    NOT in combination with other aberrations

    Df(1)HF368 hemizygous embryos exhibit head and thorax defects similar to tsg loss of function mutants.

    With a very low penetrance, Df(1)HF368 hemizygous embryos show subtle defects in segmentation, including partial fusion of denticle band pairs in the register seen for Ten-m mutants.

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

    Heterozygous females exhibit reduced viability and fertility.

    Stocks (2)
    Notes on Origin
    Discoverer

    Lefevre.

     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (6)
    Reported As
    Name Synonyms
    Secondary FlyBase IDs
      References (26)