Open Close
General Information
Symbol
Df(2R)WMG
Species
D. melanogaster
Name
FlyBase ID
FBab0002046
Feature type
Computed Breakpoints include
52A9-52A10;52D9-52D15
Deleted Segment
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to wild type)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data
bk1 << l(2)52ACh << l(2)52Db << bk2 << Got1
Genetic mapping information
Comments
Comments on Cytology
Limits of break 1 from polytene analysis (FBrf0054158) Limits of break 2 from polytene analysis (FBrf0046776)
Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations
The Df(2R)WMG 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).
Mutant embryos show complete fusion of the longitudinal and commissural nerve trunks - few intersegmental connections are maintained.
Acts as a dosage sensitive maternal modifier of run : causes tergite defects in greater than 50% of run3 heterozygotes.
Homozygous embryos show defects in segmentation, germband retraction, dorsal closure and head involution. Elongation of Malpighian tubule material is variable.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Stocks (2)
Notes on Origin
Discoverer
Gelbart.
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (4)
Reported As
Name Synonyms
Secondary FlyBase IDs
  • FBab0002047
References (31)