Aberration Dmel\Df(3R)p712

General Information
Symbol	Dmel\Df(3R)p712	Species	D. melanogaster
Name	Deficiency (3R) pink	FlyBase ID	FBab0002866
Feature type	deficient_translocation

Computed Breakpoints include	84D4-84D6;85B6;25D
Deleted segment	84D4-6--85B6
Sequence coordinates
Member of large scale dataset(s)
Recent Updates
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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	X ray
Class of aberration (relative to progenitor)	chromosomal_deletion (Bhadra and Birchler, 1996, Harbecke and Lengyel, 1995, Prout et al., 1997) deficient_translocation (Kemphues et al., 1983, )
Breakpoints	84D4-84D6;85B5;25D (Kemphues et al., 1983) 84D4-84D6;85B6 (Harbecke and Lengyel, 1995, Bhadra and Birchler, 1996, Prout et al., 1997)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data	l(3)02732 << bk1 << l(3)neo35 << p << bk2 << l(3)00281 << bk3 << stck
Genetic mapping information
Comments
Comments on Cytology
	Limits of break 1 from polytene analysis (citation unavailable) Limits of break 2 from polytene analysis (FBrf0082073) Limits of break 3 from polytene analysis (citation unavailable)
Sequence Crossreferences
DDBJ / EMBL / GenBank	DNA sequence Protein sequence Name
Gene Deletion & Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted	bel (BDGP Project Members, 1994-1999, Spradling et al., 1999, Szeged Stock Center, 1998-) Coq2 (Liao et al., 2006) Dhod (Spradling et al., 1999) grn (Spradling et al., 1999, BDGP Project Members, 1994-1999) hb (Harbecke and Lengyel, 1995) l(3)S011028 (Szeged Stock Center, 1998-) Mcm2 (Spradling et al., 1999, BDGP Project Members, 1994-1999) mtg (Szeged Stock Center, 1998-) puc (Pastor-Pareja et al., 2004, Spradling et al., 1999, BDGP Project Members, 1994-1999) sr (BDGP Project Members, 1994-1999) stck (Prout et al., 1997) unc-45 (Spradling et al., 1999, BDGP Project Members, 1994-1999)
Molecular Data
Genes NOT Deleted / Disrupted
Complementation Data
	Atpα (BDGP Project Members, 1994-1999) bnl (BDGP Project Members, 1994-1999) Dlc90F (BDGP Project Members, 1994-1999) hty (Szeged Stock Center, 1998-) l(3)00281 (Spradling et al., 1999, BDGP Project Members, 1994-1999) l(3)02693 (BDGP Project Members, 1994-1999) l(3)02732 (Spradling et al., 1999, BDGP Project Members, 1994-1999) l(3)j1B9 (Spradling et al., 1999, BDGP Project Members, 1994-1999) l(3)j15E7 (BDGP Project Members, 1994-1999) l(3)neo35 (Spradling et al., 1999, BDGP Project Members, 1994-1999) l(3)s3246 (BDGP Project Members, 1994-1999) Mow (Bhadra and Birchler, 1996) Rel (Spradling et al., 1999, BDGP Project Members, 1994-1999) sdl (Spradling et al., 1999) ttk (BDGP Project Members, 1994-1999) twr (Spradling et al., 1999)
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	The distal half of the salivary gland turns but the proximal half does not in embryos homozygous for Df(3R)p712 by stage 14. (Jattani et al., 2009) Has a partially penetrant dominant cuticle phenotype. (Cox et al., 2000) Dominantly enhances the Kr^If-1/+ eye phenotype. (Carrera et al., 1998) Intermediate second site non-complementing phenotype with zip^mhc-c6.1 (though not zip^Ebr): malformed phenotype penetrance 25-75%. (Halsell and Kiehart, 1998) Shows no maternal enhancement of dpp^hr4. (Nicholls and Gelbart, 1998) Deficient embryos show an uninterpretable mutant midgut phenotype. (Bilder and Scott, 1995) Homozygous embryos are very abnormal compared to wild-type and inner organs are reduced in size. (Harbecke and Lengyel, 1995)
Stocks ( 3 )
Bloomington	1968 Df(3R)p712, red¹ e¹/TM3, Sb¹ Ser¹
Kyoto	106728 Df(3R)p712, red¹ e¹/TM3, Sb¹ Ser¹ 103358 Df(3R)p712, red¹ e¹ / TM3, Sb¹ Ser¹
Notes on Origin
Discoverer

Balancer / Genotype Variants of the Aberration

Separable Components

Other Comments
	The Df(3R)p712 chromosome acts as a dominant weak suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{w^var}KR3-2", a stable "brown-red" variant of the P{3'WP-2,w^var}2Lt insertion), but this is a false positive result (the suppressor is not within the bounds of the deficient region) because the region of the deficiency is covered by one or more nonsuppressing deficiencies. (Mason et al., 2004)
Synonyms & Secondary IDs ( 4 )
Reported As
Symbol Synonym	Df(3R)p712 (Provost et al., 2006, Pastor-Pareja et al., 2004, Liao et al., 2006, Goodliffe et al., 2007, Bejarano et al., 2008, Jattani et al., 2009, Slack et al., 2006) Df(3R)p⁷¹² (Bhadra and Birchler, 1996) p712 (Heeger et al., 2005)
Name Synonym	Deficiency (3R) pink
Secondary FlyBase IDs

References ( 37 )

Generate a list of	All references relating to this aberration ( 37 )

List References by type	Research paper ( 33 ) Personal communication to FlyBase ( 1 ) FlyBase analysis ( 1 ) Stock list ( 1 ) Book ( 1 )
Recent research papers (0)
	All research papers listed in FlyBase were published before 2011 Show research papers ...