FB2024_03 , released June 25, 2024
Aberration: Dmel\Df(2R)nap9
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General Information
Symbol
Df(2R)nap9
Species
D. melanogaster
Name
FlyBase ID
FBab0002190
Feature type
Also Known As
Df(2R)nap9
Computed Breakpoints include

42A1-42A2;42E6-42F1

Genomic Maps
Sequence coordinates
2R:5,798,246..5,852,960 (Df(2R)nap9:bk1)
2R:7,000,231..7,009,943 (Df(2R)nap9: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

42A1-42A2;42E5-42E7

42A1-42A2;42E5-42F1

42A1-42A2;42E6-42F1

Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

ap << bk1 << Eb1 << bk2

Genetic mapping information
Comments
Comments on Cytology

The left Df(2R)nap9 breakpoint lies within dpr12 or Or42b or in the region between dpr12 and Or42b, and lies in the range 2R:1685751..1740465 (R5) (predicted cytology: 41F11-42A1).

The right Df(2R)nap9 breakpoint likely lies within Tsp42Ec or Tsp42Ed or in the region between these genes, and lies in the range 2R:2887736..2897448 (R5) (predicted cytology: 42B2).

Left limit of break 1 from polytene analysis (FBrf0075275) Right limit of break 1 from inclusion of Src42A (FBrf0102064) Left limit of break 2 from polytene analysis (FBrf0098246) Right limit of break 2 from polytene analysis (FBrf0075275)

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

The Df(2R)nap9 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).

No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.

Stocks (3)
Notes on Origin
Discoverer
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (4)
References (35)