Aberration Dmel\Df(1)16-3-35

General Information
Symbol	Dmel\Df(1)16-3-35	Species	D. melanogaster
Name		FlyBase ID	FBab0000189
Feature type	chromosomal_deletion

Computed Breakpoints include	19D3;19E3
Deleted segment	19D3--19E3
Map ( GBrowse )	Untitled Document Error No matching regions found.
Sequence coordinates	X:20,665,792..20,668,050 [-] (Df(1)16-3-35:bk2) (Krishnan et al., 1993)
Member of large scale dataset(s)
Recent Updates
Description	What does this section display? This section contains items that were added to this record for each release. It currently only tracks new links between this FlyBase report and other FlyBase data classes (e.g. genes, references, stocks) or controlled vocabulary terms (e.g. GO, anatomy terms). What does this section not display? This section does not currently display links that were removed or gene model changes.
Update Feed	Click the icon below to subscribe to this FlyBase record and receive updates automatically through your feed reader.
FB2013_03
FB2013_02
All updates	Click here to see a list of all updates to this record from FB2010_08 and on.
Nature of the Aberration
Cytological Order
Progenitor
Mutagen	neutrons
Class of aberration (relative to progenitor)	chromosomal_deletion (Balakrishnan and Rodrigues, 1991, Simmons et al., 1984)
Breakpoints	19D2-19D3;19E6-19E7 (Simmons et al., 1984) 19D3;19E3 (Balakrishnan and Rodrigues, 1991)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data	l(1)19Cc << bk1 << mal << bk2 hits shakB
Genetic mapping information
Comments	Df(1)16-3-35 proximal breakpoint maps approximately 7kb 5' to exon A of shakB transcript S2.2. (Crompton et al., 1995) Breakpoint(s) molecularly mapped Df(1)16-3-35 breaks within an intron of the shakB locus. (Krishnan et al., 1993)
Comments on Cytology
	Left limit of break 1 from polytene analysis (FBrf0054538) Right limit of break 1 from polytene analysis (FBrf0040956) Limits of break 2 from polytene analysis (FBrf0054538)
Sequence Crossreferences
DDBJ / EMBL / GenBank	DNA sequence Protein sequence Name
Gene Deletion & Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted	l(1)19Eg (Kramers et al., 1991) lf (Kramers et al., 1983) mal (Miklos et al., 1987, Perrimon et al., 1989, Torres and Sanchez, 1992) mell (Miklos et al., 1987, Perrimon et al., 1989, Torres and Sanchez, 1992) Npc1b (Paradi et al., 1983, Kramers et al., 1983) run (Paradi et al., 1983, Kramers et al., 1983, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991, Torres and Sanchez, 1992) shakB (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)
Molecular Data
Genes NOT Deleted / Disrupted
Complementation Data
	eo (Munoz, 2003.12.10, Paradi et al., 1983, Eeken et al., 1985, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) fliI (Paradi et al., 1983, Kramers et al., 1983, Eeken et al., 1985, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) fog (Paradi et al., 1983, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) Hlc (Eeken et al., 1985, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) intro (Munoz, 2004.1.5, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) l(1)19Ca (Paradi et al., 1983, Kramers et al., 1983, Kramers et al., 1991) l(1)19Cb (Paradi et al., 1983, Kramers et al., 1983, Kramers et al., 1991) l(1)19Cc (Paradi et al., 1983, Kramers et al., 1983, Kramers et al., 1991) l(1)19Cd (Kramers et al., 1991) l(1)19Ed (Paradi et al., 1983, Kramers et al., 1983, Eeken et al., 1985, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) l(1)19Fb (Miklos et al., 1987, Perrimon et al., 1989) l(1)19Fe (Eeken et al., 1985, Kramers et al., 1991) l(1)19Fh (Kramers et al., 1991) l(1)20Ag (Kramers et al., 1991) l(1)20Ah (Kramers et al., 1991) l(1)20Ai (Kramers et al., 1991) l(1)20Aj (Kramers et al., 1991) l(1)20Bd (Kramers et al., 1991) l(1)20BFa (Kramers et al., 1991) l(1)20Ca (Paradi et al., 1983, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) l(1)20Cb (Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) l(1)20Cc (Kramers et al., 1991) l(1)carot3 (Kramers et al., 1991) lf (Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) lfl (Kramers et al., 1983, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) mal (Kramers et al., 1983, Kramers et al., 1991) mel (Kramers et al., 1983, Kramers et al., 1991) mst (Paradi et al., 1983, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) Npc1b (Perrimon et al., 1989, Miklos et al., 1987, Torres and Sanchez, 1992, Kramers et al., 1991, Munoz, 2004.1.5) slgA (Miklos et al., 1987, Perrimon et al., 1989) sol (Miklos et al., 1987, Perrimon et al., 1989) soz (Eeken et al., 1985, Perrimon et al., 1989, Kramers et al., 1991) sph (Munoz, 2004.1.5, Paradi et al., 1983, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) stnA (Munoz, 2004.1.5, Paradi et al., 1983, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) stnB (Perrimon et al., 1989) su(f) (Paradi et al., 1983, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) sw (Paradi et al., 1983, Kramers et al., 1983, Eeken et al., 1985, Kramers et al., 1991) tuh1 (Perrimon et al., 1989) unc (Miklos et al., 1987, Perrimon et al., 1989) uncl (Paradi et al., 1983, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991) vao (Miklos et al., 1987, Perrimon et al., 1989) wap (Paradi et al., 1983, Eeken et al., 1985, Miklos et al., 1987, Perrimon et al., 1989, Kramers et al., 1991)
Molecular Data
Genes Duplicated
Complementation Data
Molecular Data
Genes NOT Duplicated
Complementation Data
Molecular Data
Related Comments

Phenotypic Data
In combination with other aberrations	Inferred to overlap with: Df(1)16-1-88. (Munoz, 2004.1.5) Df(1)16-3-35/Df(1)A118 viable (Yamamoto and Miklos, 1987)
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. (Baird et al., 1993) Display lethal phenotype when in combination with Df(1)N71. (Torres and Sanchez, 1992) Heterozygotes have an extreme shakB mutant phenotype: full set of neuronal defects. (Baird et al., 1990)
Stocks ( 0 )

Notes on Origin
Discoverer	Munoz.

Balancer / Genotype Variants of the Aberration

Separable Components

Other Comments
	Molecular analysis shows the proximal breakpoint is in shakB near the 5' end. (Krishnan et al., 1995)
Synonyms & Secondary IDs ( 3 )
Reported As
Symbol Synonym	16-3-35 (Sanchez et al., 1994) Df16-3-35 (Kramers et al., 1991) Df(1)16-3-35
Name Synonym
Secondary FlyBase IDs

References ( 24 )

Generate a list of	All references relating to this aberration ( 24 )

List References by type	Research paper ( 17 ) Review ( 1 ) Personal communication to FlyBase ( 3 ) Abstract ( 1 ) FlyBase analysis ( 1 ) Book ( 1 )
Recent research papers (0)
	All research papers listed in FlyBase were published before 2011 Show research papers ...
Recent reviews (0)
	All reviews listed in FlyBase were published before 2011 Show reviews ...

Aberration Dmel\Df(1)16-3-35

Error