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General Information
Symbol
Df(1)C246
Species
D. melanogaster
Name
FlyBase ID
FBab0000355
Feature type
Also Known As
C246
Computed Breakpoints include

11D1;12A1

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

gs(1)N41 << bk1 << l(1)11Dc << Gpt << bk2 << up

Genetic mapping information
Comments

This deletion removes multiple ribosomal protein-coding genes (in addition to other genes).

Comments on Cytology

Left limit of break 1 from polytene analysis (citation unavailable) Right limit of break 1 from inclusion of rad (FBrf0053305) Left limit of break 2 from polytene analysis (FBrf0034402) Right limit of break 2 from polytene analysis (FBrf0086390)

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
 
Phenotypic Data
In combination with other aberrations

YSX.YL, Df(1)C246, In(1)EN, y M/C(1;Y)2, Df(1)gl In(1)EN, y g f B females are viable, yellow and Minute (Schalet).

NOT in combination with other aberrations

Flies heterozygous for the deletion show a Minute bristle phenotype.

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

Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.

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

Shows no maternal enhancement of dpphr4.

Dominantly causes tergite defects in less than 50% of run3 heterozygotes.

Deficient embryos show an uninterpretable mutant midgut phenotype.

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

Hemizygous embryos were examined with polarised light microscopy and antibody staining: muscle pattern incomplete due to muscle absences and detachments.

Mutants show a moderate Minute phenotype.

Stocks (2)
Notes on Origin
Discoverer

Lefevre.

 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (6)
References (49)