FB2025_01 , released February 20, 2025
Aberration: Dmel\Df(3L)st8P
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General Information
Symbol
Df(3L)st8P
Species
D. melanogaster
Name
Deficiency (3L) scarlet
FlyBase ID
FBab0002435
Feature type
chromosomal_deletion
Computed Breakpoints include

72E4;73B4

Features within 72E4--73B4
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
In(3L)P
Mutagen
X ray
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Duffy et al., 1996, Pauli et al., 1995, Tearle et al., 1989)
Breakpoints

72E4;73B4

(Duffy et al., 1996, Pauli et al., 1995, Tearle et al., 1989)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

bk1 << l(3)73Aa << Abl << bk2 << db

Genetic mapping information
Comments
Comments on Cytology

All limits from polytene analysis (FBrf0049915)

Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
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.
    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

    Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.

    (Coyne et al., 1998)

    Dominantly causes tergite defects in less than 50% of run3 heterozygotes.

    (Duffy et al., 1996)

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

    (Pauli et al., 1995)
    Stocks (2)
    Notes on Origin
    Discoverer

    Bonner.

     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (3)
    Reported As
    Symbol Synonym
    Df(3L)Pst8
    Df(3L)st8P
    (Barbash and Lorigan, 2007, Jung et al., 2007)
    Name Synonyms
    Deficiency (3L) scarlet
    Secondary FlyBase IDs
      References (9)