FlyBase Aberration Report: Dmel\Df(2L)ED729

General Information

Symbol

Df(2L)ED729

Species

D. melanogaster

Name

FlyBase ID

FBab0032473

Feature type

chromosomal_deletion

Computed Breakpoints include

[31B1-31B1];[31D7-31D7];

Features within 31B1--31D7

Genomic Maps

JBrowse

Sequence coordinates

2L:10,220,877..10,220,877 (Df(2L)ED729:bk1)

(DrosDel Project, 2007.6.25)

2L:10,321,777..10,321,777 (Df(2L)ED729:bk2)

(DrosDel Project, 2007.6.25)

Member of large scale dataset(s)

Dfs_DrosDel_set1

A set of isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Initial core set of 209 isogenic deletions provides ~60% euchromatic genome coverage.

(Ryder et al., 2007)

Nature of Aberration

Cytological Order

Progenitor

P{RS3r}CB-6516-3

(Ryder and Roote, 2005.11.4)

P{RS5r}5-SZ-4008

(Ryder and Roote, 2005.11.4)

Mutagen

FLPase

(Ryder and Roote, 2005.11.4)

Class of aberration (relative to wild type)

chromosomal_deletion

(FlyBase, 2007)

Class of aberration (relative to progenitor)

chromosomal_deletion

(Ryder and Roote, 2005.11.4, Ryder, 2003.6.17)

Breakpoints

31B1;31D7

(FlyBase Curators, 2008)

Causes alleles

Carries alleles

Transposon Insertions

P{3'.RS5+3.3'}ED729

(Ryder and Roote, 2005.11.4)

Formalized genetic data

Genetic mapping information

Comments

Comments on Cytology

Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k06324^k06324 and P{lacW}me31B^k06607 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}nmd⁰⁸⁷⁷⁴ and P{lacW}RnrL^k06709

Sequence Crossreferences

DDBJ / EMBL / GenBank

DNA sequence

Protein sequence

Gene Deletion and Duplication Data

Genes Deleted / Disrupted

Complementation Data

Completely deleted / disrupted

l(2)SH0834

(Cook, 2014.5.2)

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 (37)

Related Comments

Phenotypic Data

In combination with other aberrations

NOT in combination with other aberrations

The rough eye phenotype observed in adults expressing Magi^{Scer\UAS.T:Avic\GFP} under the control of Scer\GAL4^GMR.PU is not modified by combination with single copy of Df(2L)ED729.

(Zaessinger et al., 2015)

Stocks (2)

Bloomington

24134

w¹¹¹⁸; Df(2L)ED729, P{3'.RS5+3.3'}ED729/SM6a

Kyoto

150095

w¹¹¹⁸; Df(2L)ED729 / SM6a

Notes on Origin

Discoverer

Balancer / Genotype Variants of the Aberration

Separable Components

Other Comments

Synonyms and Secondary IDs (2)

Reported As

Symbol Synonym

Df(2L)ED729

(Tsai et al., 2025, Charroux and Royet, 2022, Sanaki et al., 2020, Walther et al., 2020, Hope et al., 2019, Ripp et al., 2018, Zaessinger et al., 2015, Cook, 2014.5.2, FlyBase Curators, 2008)

Df_2L_ED729

(Nelson et al., 2016)

Name Synonyms

Secondary FlyBase IDs

References (16)

Report Sections

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