FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
Aberration: Dmel\Df(2L)BSC323
Open Close
General Information
Symbol
Df(2L)BSC323
Species
D. melanogaster
Name
FlyBase ID
FBab0045130
Feature type
chromosomal_deletion
Computed Breakpoints include

[33A5-33A5];[33C1-33C1];

Features within 33A5--33C1
Genomic Maps
Sequence coordinates
2L:11,870,517..11,870,517 (Df(2L)BSC323:bk1)
(Bloomington Drosophila Stock Center, 2008.8.7)
2L:12,055,450..12,055,450 (Df(2L)BSC323:bk2)
(Bloomington Drosophila Stock Center, 2008.8.7)
Member of large scale dataset(s)
Dfs_BSC_set2

A set of ~800 largely isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Designed to fill gaps in deletion coverage and breakpoint placement; also used to replace older available deficiencies that have not been molecularly mapped.

(Cook et al., 2012)
Nature of Aberration
Cytological Order
Progenitor
PBac{WH}Pde1cf02409
(Christensen et al., 2007.10.29)
P{XP}d10374
(Christensen et al., 2007.10.29)
Mutagen
FLPase
(Christensen et al., 2007.10.29)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Christensen et al., 2007.10.29)
Breakpoints

33A5;33C1

(FlyBase Curators, 2008)
Causes alleles
Carries alleles
Transposon Insertions
P+PBac{XP5.WH5}BSC323
(Christensen et al., 2007.10.29)
Formalized genetic data
Genetic mapping information
Comments

Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.

(Bloomington Drosophila Stock Center, 2008.8.7)
Comments on Cytology

Exelixis, Inc. determined the insertion site of P{XP}d10374 to be at Release 3 genomic coordinate 12044040 on chromosome arm 2L. The Gene Disruption project determined the insertion site of P{XP}d10374 to be at Release 3 genomic coordinate 12044441 on arm 2L. This corresponds to 33C1 on both the Release 3 and 5 genome maps. The predicted position of PBac{WH}CG31757f02409 on the Release 5 map is 33A5. Consequently, the cytological breakpoints of Df(2L)BSC323 are predicted to be 33A5;33C1.

(Christensen et al., 2007.10.29)
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 (36)
Phenotypic Data
In combination with other aberrations

Inferred to overlap with: Df(2L)Exel6030.

(Christensen et al., 2007.10.29)

Inferred to overlap with: Df(2L)Exel6031.

(Christensen et al., 2007.10.29)
NOT in combination with other aberrations

Df(2L)BSC323 is homozygous lethal.

(Bergwitz et al., 2012)
Stocks (1)
Notes on Origin
Discoverer
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 

The presence of P+PBac{XP5.WH5}BSC323 was verified using the PCR methods and primers described in FBrf0175003.

(Christensen et al., 2007.10.29)
Synonyms and Secondary IDs (2)
References (10)