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General Information
Symbol
Df(3L)vin5
Species
D. melanogaster
Name
Deficiency (3L) vin
FlyBase ID
FBab0002457
Feature type
Also Known As
Df(3L)vin5
Computed Breakpoints include
68A2;69A1
Deleted Segment
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Class of aberration (relative to wild type)
Breakpoints
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data
rs << bk1 << grr << l(3)69Aa << bk2 << Est-6
Genetic mapping information
Comments
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Comments on Cytology
Left limit of break 1 from polytene analysis (FBrf0080317) Right limit of break 1 from inclusion of klu (FBrf0098281) Left limit of break 2 from polytene analysis (FBrf0082073) Right limit of break 2 from non-inclusion of Est-6 (FBrf0048238)
Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
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
Inferred to overlap with: Df(3L)BSC379.
NOT in combination with other aberrations
The salivary gland distal tip does not initiate turning and migration in embryos homozygous for Df(3L)vin5 by stage 14.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Df(3L)vin5 embryos show defects in tracheal cell migration.
The Df(3L)vin5 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).
Heterozygosity for Df(3L)vin5 results in 3.8% X chromosome nondisjunction and 0.3% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
The level of 7-monoenes is normal in heterozygous males. The level of 7,11-dienes is significantly increased in heterozygous females compared to controls.
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 reduced anal pads. Midgut constrictions do not form, the hindgut is shorter than normal and Malpighian tubules form short buds.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Fertile when heterozygous with haync2.
Stocks (2)
Notes on Origin
Discoverer
 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (5)
References (61)