[71A2-71A2];[71B2-71B2];
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.
71A3;71B3
71A2;71B2
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Breakpoint based on release 3 sequence coordinate from Parks et al., 2004 (FBrf0174230), converted to release 5 coordinate.
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Inferred to overlap with: Df(3L)BSC441.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Limits computationally determined from location of progenitor P insertion on genome sequence between P{lacW}cp309s2172/P{lacW}l(3)j2A2j2A2 and P{EP}Tfb2EP572