FB2025_01 , released February 20, 2025
Aberration: Dmel\Df(3R)9A99
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General Information
Symbol
Df(3R)9A99
Species
D. melanogaster
Name
FlyBase ID
FBab0002481
Feature type
Also Known As
9A99
Computed Breakpoints include
Genomic Maps
Sequence coordinates
3R:6,652,681..6,657,124 [-] (Df(3R)9A99:bk1)
3R:6,872,548..6,874,435 [-] (Df(3R)9A99:bk2)
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

83F2-84A1;84B1-84B2

Carries alleles
Transposon Insertions
Formalized genetic data

bk1 << bcd << anon-84Bd << bk2 << Antp

Genetic mapping information
Comments

Breakpoint 1 was linked to an EcoRI-HindIII restriction fragment from map. The position of the restriction fragment on the reference sequence was inferred by a FlyBase curator.

Breakpoint 2 was linked to a HindIII-BamHI restriction fragment. The position of the restriction fragment on the reference sequence was inferred by a FlyBase curator.

Breakpoint(s) molecularly mapped

Proximal breakpoint between coordinates +170 and +180 on DNA map of region 84B1-2 (Garber et al., 1983).

Comments on Cytology

Limits of break 1 from polytene analysis (FBrf0039287) Left limit of break 2 from inclusion of Scr (FBrf0042438) Right limit of break 2 from non-inclusion of Antp (FBrf0042438)

Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
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 (43)
Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations

The Df(3R)9A99 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).

Shows dominant enhancement of dominant haltere phenotype caused by Ubx195 and Ubx9.22.

Heterozygosity for this deletion suppresses the mutant ovarian phenotype of ovoD2.

Phenocopies of the bcd mutant phenotype are produced if cytoplasm is removed from the anterior tip of embryos derived from heterozygous females.

Stocks (3)
Notes on Origin
Discoverer

G. Jurgens.

 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (17)