FlyBase Aberration Report: Dmel\Df(3R)T-32

General Information

Symbol

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

Features within 86D9--87C4 (Estimated cytology)

Genomic Maps

JBrowse

Sequence coordinates

3R:11,246,530..11,269,696 (Df(3R)T-32:bk1)

(Cook et al., 2010.2.12)

3R:12,660,496..12,673,277 (Df(3R)T-32:bk2)

(Cook et al., 2010.2.12)

Member of large scale dataset(s)

Nature of Aberration

Cytological Order

Progenitor

Tp(1;3)TE86Ea

Mutagen

Class of aberration (relative to wild type)

chromosomal_deletion

(Cook et al., 2010.2.12, FlyBase, 2007)

Class of aberration (relative to progenitor)

chromosomal_deletion

(Bhadra and Birchler, 1996, Duffy et al., 1996, Harbecke and Lengyel, 1995, Pauli et al., 1995)

Breakpoints

86E2-86E4;87C6-87C7

(Bhadra and Birchler, 1996, Duffy et al., 1996, Harbecke and Lengyel, 1995, Pauli et al., 1995)

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

Gene Deletion and 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)

Partially deleted / disrupted

Molecular Data

Completely deleted

Partially deleted

Genes NOT Deleted / Disrupted

Complementation Data

Molecular Data

Genes Duplicated

Complementation Data

Completely duplicated

Partially duplicated

Molecular Data

Completely duplicated

Partially duplicated

Genes NOT Duplicated

Complementation Data

Molecular Data

Affected Genes Inferred by Location

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 and Secondary IDs (5)

Reported As

Symbol Synonym

BL3003

(Wayne and McIntyre, 2002)

Df(3R) T-32

(Fiehler and Wolff, 2008)

Df(3R)T-32

(Bernardoni et al., 2019, Munoz-Soriano et al., 2012, Fernandes and Rao, 2011, Cook et al., 2010.2.12, Jattani et al., 2009, Goodliffe et al., 2007, Neuburger et al., 2006, Sarfare et al., 2005)

Df(3R)TE32

(LaJeunesse et al., 2001, Harbecke and Lengyel, 1995, Pauli et al., 1995, Castrillon et al., 1993, Vaessin et al., 1991)

Df(3R)Te32

(Duffy et al., 1996)

Name Synonyms

Secondary FlyBase IDs

References (42)

Report Sections

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