FlyBase Aberration Report: Dmel\Df(1)17-148

General Information

Symbol

Df(1)17-148

Species

D. melanogaster

Name

FlyBase ID

FBab0000191

Feature type

chromosomal_deletion

Also Known As

17-148

Computed Breakpoints include

20C;20E1-h26

Features within 20C--h26

Sequence coordinates

Member of large scale dataset(s)

Nature of Aberration

Cytological Order

Progenitor

Mutagen

neutron

(Schalet and Lefevre, 1973)

X ray

(Rahman and Lindsley, 1981)

Class of aberration (relative to wild type)

chromosomal_deletion

(FlyBase, 2007)

Class of aberration (relative to progenitor)

chromosomal_deletion

Breakpoints

Causes alleles

Carries alleles

Transposon Insertions

Formalized genetic data

l(1)20Ca << bk1 << l(1)20Cb << su(f) << bk2 << bb

Genetic mapping information

Comments

Comments on Cytology

Complementation with stnA and l(1)20Ca not tested.

(Rahman and Lindsley, 1981)

Left limit of break 1 from non-inclusion of l(1)20Ca (FBrf0024685) Right limit of break 1 from inclusion of l(1)20Cb (FBrf0024685) Left limit of break 2 from inclusion of su(f) (FBrf0024685) Right limit of break 2 from non-inclusion of bb (FBrf0024685)

Sequence Crossreferences

DDBJ / EMBL / GenBank

DNA sequence

Protein sequence

Gene Deletion and Duplication Data

Genes Deleted / Disrupted

Complementation Data

Completely deleted / disrupted

l(1)20Cb

(Perrimon et al., 1989, Rahman and Lindsley, 1981, Schalet and Lefevre, 1973)

sph

(Perrimon et al., 1989, Rahman and Lindsley, 1981)

su(f)

(Prud'homme et al., 1995, Perrimon et al., 1989, Rahman and Lindsley, 1981, Schalet and Lefevre, 1973)

Partially deleted / disrupted

Molecular Data

Completely deleted

Partially deleted

Genes NOT Deleted / Disrupted

Complementation Data

(Rahman and Lindsley, 1981, Schalet and Lefevre, 1973)

Ddx56

(Prud'homme et al., 1995, Rahman and Lindsley, 1981)

eor

(Prud'homme et al., 1995, Perrimon et al., 1989, Rahman and Lindsley, 1981)

fog

(Perrimon et al., 1989, Rahman and Lindsley, 1981)

intro

(Prud'homme et al., 1995, Perrimon et al., 1989, Rahman and Lindsley, 1981)

l(1)20Ca

(Perrimon et al., 1989, Schalet and Lefevre, 1973)

l(1)carot2

(Prud'homme et al., 1995)

lncRNA:flam

(Prud'homme et al., 1995)

mal

(Prud'homme et al., 1995)

mel

(Prud'homme et al., 1995)

mst

(Prud'homme et al., 1995)

soz

(Perrimon et al., 1989)

stnA

(Perrimon et al., 1989)

stnB

(Perrimon et al., 1989)

tuh1

(Prud'homme et al., 1995, Perrimon et al., 1989)

uncl

(Perrimon et al., 1989, Rahman and Lindsley, 1981)

wap

(Prud'homme et al., 1995, Perrimon et al., 1989, Rahman and Lindsley, 1981)

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 (0)

If no genes are listed here, it may be because the affected region is very large. The JBrowse insert above may show an error for the same reason, and other FlyBase tools such as CytoSearch may also fail for large regions. You can contact FlyBase for more help.
In these cases, there will be no "Export to Hitlist" button to the left.

Related Comments

Phenotypic Data

In combination with other aberrations

Lethal with Df(1)n23. Inferred to overlap with: Df(1)n23. Viable with Df(1)17-439.

(Munoz, 2004.1.5)

NOT in combination with other aberrations

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

5960

Df(1)17-148/Binsn/Dp(1;Y)mal⁺

Kyoto

108505

Df(1)17-148/Binsn/Dp(1;Y)mal⁺

Notes on Origin

Discoverer

Munoz.

Balancer / Genotype Variants of the Aberration