|Computed Breakpoints include||[99F6-99F6];[99F7-99F7];|
|Map ( GBrowse )||
|Member of large scale dataset(s)|
A set of isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Initial set of 519 isogenic deletions provides 56% genome coverage.
The current Exelixis collection at the Bloomington Stock Center differs from the original described in FBrf0175003: a significant number were shown not to carry a deletion and have been removed from the collection; a number of stocks have been lost; a number of additional deletions are included that were generated after publication.
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|Nature of the Aberration|
|Class of aberration (relative to progenitor)|
|Formalized genetic data|
|Genetic mapping information|
|Comments on Cytology|
|Gene Deletion & Duplication Data|
|Genes Deleted / Disrupted|
|Genes NOT Deleted / Disrupted|
|Genes NOT Duplicated|
|In combination with other aberrations|
|NOT in combination with other aberrations|
Df(3R)Exel6216 embryos that are at stage 15 or above show defects in the apical surfaces of the secretory cells. These embryos also show gross irregularities in the salivary gland lumena; the lumena have regions of expansion and constriction, as well as regions where the tubes appear closed. Cell polarity and other aspects of gland morphology are not affected.
|Stocks ( 1 )|
|Notes on Origin|
|Balancer / Genotype Variants of the Aberration|
|Synonyms & Secondary IDs ( 1 )|
|Secondary FlyBase IDs|
|References ( 10 )|
|Personal communication to FlyBase|