|Also Known As||VW3|
|Computed Breakpoints include||76A3;76B2|
|Member of large scale dataset(s)|
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|All updates||Click here to see a list of all updates to this record from FB2010_08 and on.|
|Nature of the Aberration|
|Class of aberration (relative to progenitor)|
|Formalized genetic data||rept << bk1 << M(3)76A << bk2 << Su(Tpl)|
|Genetic mapping information|
|Comments on Cytology|
All limits from polytene analysis (FBrf0036112)
|Gene Deletion & Duplication Data|
|Genes Deleted / Disrupted|
|Completely deleted / disrupted|
|Genes NOT Deleted / Disrupted|
|Genes NOT Duplicated|
|In combination with other aberrations|
|NOT in combination with other aberrations|
Heterozygosity for Df(3L)VW3 results in 0.9% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Deficient embryos show a mutant midgut phenotype: visceral mesoderm does not develop.
Homozygous embryos do not complete dorsal closure and gastrulation is often abnormal.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
|Stocks ( 1 )|
|Notes on Origin|
|Balancer / Genotype Variants of the Aberration|
|Synonyms & Secondary IDs ( 3 )|
|Secondary FlyBase IDs|
|References ( 35 )|
|Generate a list of|
|List References by type|
|Recent research papers (0)|
|All research papers listed in FlyBase were published before 2011|