A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(2L)C

General Information
SymbolDmel\Df(2L)CSpeciesD. melanogaster
NameFlyBase IDFBab0001428
Feature typechromosomal_deletion
Computed Breakpoints include h35;h35-h37
Deleted segmenth35--h37
Sequence coordinates
Member of large scale dataset(s)
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Description
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FB2013_03
FB2013_02
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Nature of the Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to progenitor)
Breakpoints
h35-h37;h35-h37
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data l(2)40Fa << bk1 << l(2)40Fc << l(2)40Fg << bk2 << l(2)41Ab
Genetic mapping information
Comments
hide Comments on Cytology
Deficiency of basal heterochromatin.
Left limit of break 1 from polytene analysis (FBrf0080317) Right limit of break 1 from inclusion of cta (FBrf0054123) Left limit of break 2 from inclusion of l(2)40Fd (FBrf0028786) Right limit of break 2 from polytene analysis (FBrf0080317)
 
hide Sequence Crossreferences
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
hide Gene Deletion & Duplication Data
hide Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
Molecular Data
hide Genes NOT Deleted / Disrupted
Complementation Data
Molecular Data
hide Genes Duplicated
Complementation Data
Molecular Data
hide Genes NOT Duplicated
Complementation Data
Molecular Data
hide Related Comments
hide Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
hide Stocks ( 0 )
hide Notes on Origin
Discoverer
reconstitution of chromosome 2 by detachment of compound second chromosomes.
 
hide Balancer / Genotype Variants of the Aberration
hide Separable Components
hide Other Comments
Group C deficiencies have been generated from the progenitor genotype of C(2L)RM-SH3 in combination with C(2R)RM-SH3
hide Synonyms & Secondary IDs ( 3 )
Reported As
Symbol Synonym
Df(2L)C
 
Df(2L)PR31
Name Synonym
Secondary FlyBase IDs
hide References ( 11 )
Research paper
Pauli et al., 1995, Genetics 139(2): 713--732
Identification of regions interacting with ovoD mutations: Potential new genes involved in germline sex determination or differentiation in Drosophila melanogaster. [FBrf0080317]
Pauli et al., 1995, D. I. S. 76: 107--124
Dose dependent enhancers and suppressors of ovoD2. [FBrf0082455]
Schupbach and Wieschaus, 1991, Genetics 129: 1119--1136
Female sterile mutations on the second chromosome of Drosophila melanogaster. [FBrf0054123]
Devlin et al., 1990, Genome 33: 405--415
Identifying a single-copy DNA sequence associated with the expression of a heterochromatic gene, the light locus of Drosophila melanogaster. [FBrf0052048]
Cicchetti and Loverre, 1989, Genetica 78(3): 159--167
Analysis of an SD second chromosome from a natural population of Drosophila melanogaster. [FBrf0049871]
Ganetzky, 1977, Genetics 86: 321--355
On the components of Segregation Distortion in Drosophila melanogaster. [FBrf0030142]
Hilliker, 1976, Genetics 83: 765--782
Genetic analysis of the centromeric heterochromatin of chromosome 2 of Drosophila melanogaster: Deficiency mapping of EMS-induced lethal complementation groups. [FBrf0028786]
Hilliker and Holm, 1975, Genetics 81: 705--721
Genetic analysis of the proximal region of chromosome 2 of Drosophila melanogaster. [FBrf0027524]
Personal communication to FlyBase
BDGP Project Members, 1994-1999, BDGP Project Members, 1994-1999, Berkeley Drosophila Genome Project. (Computer file)
BDGP Project Members, 1994-1999, Berkeley Drosophila Genome Project. (Computer file) [FBrf0067338]
FlyBase analysis
FlyBase, 2007, En masse symbol-based assigment of Aberration Class with respect to wild type.
En masse symbol-based assigment of Aberration Class with respect to wild type. [FBrf0191808]
Book
Lindsley and Zimm, 1992, The Genome of Drosophila melanogaster.
The Genome of Drosophila melanogaster. [FBrf0066905]