Aberration Dmel\Df(3R)T-32

General Information
Symbol	Dmel\Df(3R)T-32	Species	D. melanogaster
Name		FlyBase ID	FBab0002655
Feature type	chromosomal_deletion
Also Known As	Df(3R)TE32

Computed Breakpoints include	86E2-86E3;87C6-87C7
Deleted segment	86D9--87C4 (Estimated cytology)
Map ( GBrowse )	Untitled Document
Sequence coordinates	3R:7,072,252..7,095,418 (Df(3R)T-32:bk1) (Cook et al., 2010.2.12) 3R:8,486,218..8,498,999 (Df(3R)T-32:bk2) (Cook et al., 2010.2.12)
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	Tp(1;3)TE86Ea
Mutagen
Class of aberration (relative to progenitor)	chromosomal_deletion (Pauli et al., 1995, Duffy et al., 1996, Bhadra and Birchler, 1996, Harbecke and Lengyel, 1995)
Breakpoints	86E2-86E4;87C6-87C7 (Pauli et al., 1995, Harbecke and Lengyel, 1995, Duffy et al., 1996, Bhadra and Birchler, 1996)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data	Su(var)3-14 << bk1 << tho << l(3)87Cb << bk2 << l(3)87Cc
Genetic mapping information
Comments
Comments on Cytology
	The left Df(3R)T-32 breakpoint lies within CG5214 or CG31386 or in the region between them, and lies in the range 3R:7072252..7095418 (R5) (predicted cytology: 86D9). (Cook et al., 2010.2.12) The right Df(3R)T-32 breakpoint lies within CG6225 or CG14395 or in the region between them, and lies in the range 3R:8486218..8498999 (R5) (predicted cytology: 87C3-87C4). (Cook et al., 2010.2.12) Left limit of break 1 from polytene analysis (FBrf0080317) Right limit of break 1 from inclusion of pros (FBrf0053403) Limits of break 2 from polytene analysis (FBrf0080317)
Sequence Crossreferences
DDBJ / EMBL / GenBank	DNA sequence Protein sequence Name
Gene Deletion & Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted	Blm (Szabad, 1998.4.8) l(3)87Ae (Szabad, 1998.4.8) l(3)87Cb (Gausz et al., 1979) ninaG (Sarfare et al., 2005) Pp1-87B (Reuter et al., 1987) pros (Balakireva et al., 2000, Vaessin et al., 1991) Prosα2 (Neuburger et al., 2006) sad (Harbecke and Lengyel, 1995) Su(var)3-13 (Reuter et al., 1987) svp (Babcock et al., 2003) tho (Castrillon et al., 1993) Vha55 (Szeged Stock Center, 1998-, Gausz et al., 1979)
Molecular Data
Genes NOT Deleted / Disrupted
Complementation Data
	E(var)87F (Reuter et al., 1987) kar (Gausz et al., 1979) l(3)87Cc (Gausz et al., 1979) l(3)87Cd (Gausz et al., 1979) l(3)S005302b (Szeged Stock Center, 1998-) l(3)S074205 (Szeged Stock Center, 1998-) l(3)S094310 (Szeged Stock Center, 1998-) l(3)S113208a (Szeged Stock Center, 1998-) Mow (Bhadra and Birchler, 1996) pros (Szeged Stock Center, 1998-) sd-4 (Babcock et al., 2003) Su(var)3-7 (Reuter et al., 1987) Su(var)3-14 (Reuter et al., 1987)
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)T-32 by stage 14. (Jattani et al., 2009) The Df(3R)T-32 chromosome does not act as a dominant 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). (Mason et al., 2004) Heterozygous males differ significantly from control males in their homo- and heterosexual courtship. These males do not discriminate between male and female target flies. (Balakireva et al., 1998) Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome. (Coyne et al., 1998) No second site non-complementing phenotype with zip^Ebr and zip^mhc-c6.1. (Halsell and Kiehart, 1998) Shows no maternal enhancement of dpp^hr4. (Nicholls and Gelbart, 1998) Dominantly causes tergite defects in less than 50% of run³ heterozygotes. (Duffy et al., 1996) 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) Suppresses In(1)w^m4h variegation (Reuter, Gausz, Gyurkovics, Friede, Bang, Spierer, Hall and Spierer, 1987, Mol. Gen. Genet. 210: 429-36)
Stocks ( 1 )
Bloomington	3003 Df(3R)T-32, cu¹ sr¹ e^s/MRS
Notes on Origin
Discoverer

Balancer / Genotype Variants of the Aberration

Separable Components

Other Comments

Synonyms & Secondary IDs ( 5 )
Reported As
Symbol Synonym	BL3003 (Wayne and McIntyre, 2002) Df(3R)T-32 (Sarfare et al., 2005, Neuburger et al., 2006, Goodliffe et al., 2007, Jattani et al., 2009, Cook et al., 2010.2.12, Munoz-Soriano et al., 2012) Df(3R) T-32 (Fiehler and Wolff, 2008) Df(3R)TE32 (LaJeunesse et al., 2001, Harbecke and Lengyel, 1995, Pauli et al., 1995, Vaessin et al., 1991, Castrillon et al., 1993, ) Df(3R)Te32 (Duffy et al., 1996)
Name Synonym
Secondary FlyBase IDs

References ( 40 )

Generate a list of	All references relating to this aberration ( 40 )

List References by type	Research paper ( 34 ) Personal communication to FlyBase ( 2 ) Abstract ( 1 ) FlyBase analysis ( 1 ) Stock list ( 1 ) Book ( 1 )
Recent research papers ( 1 )
	Munoz-Soriano et al., 2012, J. Mol. Neurosci. 48(1): 136--143 Septin 4, the Drosophila Ortholog of Human CDCrel-1, Accumulates in parkin Mutant Brains and is Functionally Related to the Nedd4 E3 Ubiquitin Ligase. [FBrf0219099] Show all research papers ...