Aberration Dmel\Df(1)DCB1-35b

General Information
Symbol	Dmel\Df(1)DCB1-35b	Species	D. melanogaster
Name		FlyBase ID	FBab0000370
Feature type	chromosomal_deletion
Also Known As	DCB1-35b

Computed Breakpoints include	19F1;20F1-h26
Deleted segment	19F1--h26
Sequence coordinates
Member of large scale dataset(s)
Recent Updates
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FB2013_03
FB2013_02
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Nature of the Aberration
Cytological Order
Progenitor
Mutagen	3H-deoxycytidine (Schalet and Lefevre, 1973) 3H-thymidine
Class of aberration (relative to progenitor)	chromosomal_deletion (Perrimon et al., 1989, Yamamoto et al., 1990, Deak et al., 1982, Pauli et al., 1995, Harbecke and Lengyel, 1995, Anand and Chandra, 1994, Craymer and Roy, 1980, Schalet and Lefevre, 1973)
Breakpoints	19E8;XLt-XRt (Yamamoto et al., 1990) 19F1--2;[] (Schalet and Lefevre, 1973) 19F1-19F2;20E-20F (Anand and Chandra, 1994, Pauli et al., 1995, Harbecke and Lengyel, 1995) 19F1;20F (Craymer and Roy, 1980, Perrimon et al., 1989) 19F;20F (Deak et al., 1982)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data	unc << bk1 << lfl << su(f) << bk2 << bb
Genetic mapping information
Comments
Comments on Cytology
	Right breakpoint is far to the right of 20A. (Schalet and Lefevre, 1973) Left limit of break 1 from polytene analysis (FBrf0024685) Right limit of break 1 from polytene analysis (FBrf0034402) Left limit of break 2 from polytene analysis (FBrf0034402) Right limit of break 2 from non-inclusion of bb (FBrf0024685)
Sequence Crossreferences
DDBJ / EMBL / GenBank	DNA sequence Protein sequence Name
Gene Deletion & Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted	bb (Zusman et al., 1985) COM (Desset et al., 2003) eo (Zusman et al., 1985, Perrimon et al., 1989, Prud'homme et al., 1995) flam (Prud'homme et al., 1995) fliI (Deak et al., 1982, Perrimon et al., 1989) fog (Zusman et al., 1985, Perrimon et al., 1989, Harbecke and Lengyel, 1995) Hlc (Perrimon et al., 1989, Prud'homme et al., 1995) intro (Schalet and Lefevre, 1973, Zusman et al., 1985, Perrimon et al., 1989, Prud'homme et al., 1995) l(1)19Fb (Schalet and Lefevre, 1973, Perrimon et al., 1989) l(1)20Ca (Schalet and Lefevre, 1973, Perrimon et al., 1989) l(1)20Cb (Schalet and Lefevre, 1973, Zusman et al., 1985, Perrimon et al., 1989) lfl (Schalet and Lefevre, 1973, Gergen and Wieschaus, 1986, Perrimon et al., 1989, Schalet, 1972) mst (Perrimon et al., 1989, Prud'homme et al., 1995) slgA (Perrimon et al., 1989) sol (Perrimon et al., 1989) soz (Perrimon et al., 1989) sph (Schalet and Lefevre, 1973, Perrimon et al., 1989) stnA (Schalet and Lefevre, 1973, Zusman et al., 1985, Perrimon et al., 1989) stnB (Zusman et al., 1985, Perrimon et al., 1989) su(f) (Schalet and Lefevre, 1973, Craymer and Roy, 1980, Gergen and Wieschaus, 1986, Perrimon et al., 1989, Prud'homme et al., 1995) tuh1 (Perrimon et al., 1989, Prud'homme et al., 1995) uncl (Schalet and Lefevre, 1973, Zusman et al., 1985, Perrimon et al., 1989) wap (Schalet and Lefevre, 1973, Zusman et al., 1985, Perrimon et al., 1989, Prud'homme et al., 1995)
Molecular Data
Genes NOT Deleted / Disrupted
Complementation Data
	bb (Schalet and Lefevre, 1973) l(1)19Ed (Zusman et al., 1985, Perrimon et al., 1989) l(1)carot2 (Prud'homme et al., 1995) lf (Perrimon et al., 1989) mal (Zusman et al., 1985, Perrimon et al., 1989, Prud'homme et al., 1995) mel (Prud'homme et al., 1995) mell (Perrimon et al., 1989) Npc1b (Zusman et al., 1985, Perrimon et al., 1989) run (Zusman et al., 1985, Gergen and Wieschaus, 1986, Tearle and Nusslein-Volhard, 1987, Perrimon et al., 1989) shakB (Zusman et al., 1985, Perrimon et al., 1989, Baird et al., 1993) unc (Schalet and Lefevre, 1973, Schalet and Lefevre, 1976, Perrimon et al., 1989) vao (Zusman et al., 1985, Perrimon et al., 1989)
Molecular Data
Genes Duplicated
Complementation Data
Molecular Data
Genes NOT Duplicated
Complementation Data
Molecular Data
Related Comments

Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations	Homozygous embryos have abnormal gut morphology; visceral mesoderm cells do not migrate dorsoventrally and dorsal midgut closure fails. (Merabet et al., 2002) No second site non-complementing phenotype with zip^Ebr and zip^mhc-c6.1. (Halsell and Kiehart, 1998) Deficient embryos show an uninterpretable mutant midgut phenotype. (Bilder and Scott, 1995) Homozygous embryos are very abnormal compared to wild-type. (Harbecke and Lengyel, 1995) Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovo^D2. (Pauli et al., 1995) No significant change in female lethality when in combination with Sxl^f1. (Anand and Chandra, 1994) Hemizygous embryos were examined with polarised light microscopy and antibody staining: muscle pattern and activity wild type within the constraints imposed by the body plan defect caused by the deletion of fog. (Drysdale et al., 1993)
Stocks ( 2 )
Bloomington	977 Df(1)DCB1-35b/FM6/Dp(1;Y)y⁺mal¹⁰⁶, mal¹⁰⁶
Kyoto	106697 Df(1)DCB1-35b/FM6/Dp(1;Y)y⁺mal¹⁰⁶, mal¹⁰⁶
Notes on Origin
Discoverer	Kaplan.

Balancer / Genotype Variants of the Aberration

Separable Components

Other Comments
	Distal heterochromatic regions are intact on the Df(1)DCB1-35b chromosome. Second breakpoint not reported. (Yamamoto et al., 1990)
Synonyms & Secondary IDs ( 4 )
Reported As
Symbol Synonym	DCB1-35b (Schalet and Lefevre, 1973, Sanchez et al., 1994) Df(1)DCB1 (Tearle and Nusslein-Volhard, 1987) Df(1)DCB-1-35b (Anand and Chandra, 1994) Df(1)DCB1-35b (Crest et al., 2007)
Name Synonym
Secondary FlyBase IDs

References ( 32 )

Generate a list of	All references relating to this aberration ( 32 )

List References by type	Research paper ( 28 ) Review ( 1 ) FlyBase analysis ( 1 ) Stock list ( 1 ) Book ( 1 )
Recent research papers (0)
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Recent reviews (0)
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