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General Information
Symbol
Df(1)JC19
Species
D. melanogaster
Name
FlyBase ID
FBab0000471
Feature type
Also Known As
JC19
Computed Breakpoints include
2F3;3C5
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
l(1)2Fc << bk1 << phl << rst << bk2
Genetic mapping information
Comments
This deletion removes multiple ribosomal protein-coding genes (in addition to other genes).
Comments on Cytology
Limits of break 1 from polytene analysis (FBrf0034402) Left limit of break 2 from inclusion of rst (FBrf0065542) Right limit of break 2 from polytene analysis (FBrf0034402)
Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Partially deleted / disrupted
Molecular Data
Partially deleted
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
Transmission rate of Dp(1;f)J21A through females to progeny is 28%, Df(1)JC19 has no effect on transmission.
NOT in combination with other aberrations
Flies heterozygous for the deletion do not 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.
Homozygous embryos have disconnected tracheae and reduced salivary glands.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
No significant change in female lethality when in combination with Sxlf1.
Hemizygous embryos were examined with polarised light microscopy and antibody staining: muscle contraction vigorous and muscle pattern wild type within constraints of body plan defect caused by deletion of gt.
Stocks (3)
Notes on Origin
Discoverer
Lefevre.
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (4)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (36)