|Computed Breakpoints include||19D3;19E3|
|Map ( GBrowse )||
No matching regions found.
X:20,665,792..20,668,050 [-] (Df(1)16-3-35:bk2)
|Member of large scale dataset(s)|
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|Nature of the Aberration|
|Class of aberration (relative to progenitor)|
|Formalized genetic data||l(1)19Cc << bk1 << mal << bk2 hits shakB|
|Genetic mapping information|
Breakpoint(s) molecularly mapped Df(1)16-3-35 breaks within an intron of the shakB locus.
|Comments on Cytology|
|Gene Deletion & Duplication Data|
|Genes Deleted / Disrupted|
|Completely deleted / disrupted|
(Paradi et al., 1983, Kramers et al., 1983, Miklos et al., 1987, Perrimon et al., 1989, Baird et al., 1990, Balakrishnan and Rodrigues, 1991, Kramers et al., 1991, Torres and Sanchez, 1992, Krishnan et al., 1993, Baird et al., 1993, Griffin et al., 1993, Krishnan et al., 1995, Crompton et al., 1995)
|Genes NOT Deleted / Disrupted|
|Genes NOT Duplicated|
|In combination with other aberrations|
|NOT in combination with other aberrations|
Heterozygotes for Df(1)16-3-35 and FM6 show reduction in the anterior-posterior extent of the medial branch of the tergotrochantral muscle motorneurone similar to that seen in shakB3/FM6.
Display lethal phenotype when in combination with Df(1)N71.
Heterozygotes have an extreme shakB mutant phenotype: full set of neuronal defects.
|Stocks ( 0 )|
|Notes on Origin|
|Balancer / Genotype Variants of the Aberration|
|Synonyms & Secondary IDs ( 3 )|
|Secondary FlyBase IDs|
|References ( 24 )|
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|List References by type|
|Recent research papers (0)|
|All research papers listed in FlyBase were published before 2011|
|Recent reviews (0)|
|All reviews listed in FlyBase were published before 2011|