FlyBase Allele Report: Dmel\su(Hw)[7]

General Information

Symbol

Dmel\su(Hw)⁷

Species

D. melanogaster

Name

FlyBase ID

FBal0016324

Feature type

allele

Associated gene

Dmel\su(Hw)

Associated Insertion(s)

Carried in Construct

Also Known As

su(Hw)^f

Key Links

Genomic Maps

JBrowse

Allele class

hypomorphic allele - genetic evidence

Mutagen

Nature of the Allele

Allele class

hypomorphic allele - genetic evidence

(Hagstrom et al., 1996, Cai and Levine, 1995, Geyer and Corces, 1992, Hoover et al., 1992)

Mutagen

ethyl methanesulfonate

(Harrison et al., 1993)

spontaneous

(Lindsley and Zimm, 1992)

Progenitor genotype

Cytology

Description

The first Cys residue of zinc finger 10 is changed to Tyr.

(Kim et al., 1996)

Point mutation in one of the Zn fingers which retains some ability to bind DNA.

(Roseman et al., 1995)

Point mutation in one of the zinc fingers.

(Dorsett, 1993)

Nucleotide substitution: G2377A. Amino acid replacement: C?Y. Substitution in the tenth zinc finger.

(Harrison et al., 1993)

Mutation of one of the zinc fingers.

(Geyer and Corces, 1992)

Southern blot normal.

(Lindsley and Zimm, 1992)

Point mutation.

(Parkhurst et al., 1988)

Mutations Mapped to the Genome

Curation Data

Type

Location

Additional Notes

References

point_mutation

3R:14,306,189..14,306,189 [-]

Nucleotide change:

G14306189A

Reported nucleotide change:

G2377A

Amino acid change:

C525Y | su(Hw)-PA; C525Y | su(Hw)-PB; C525Y | su(Hw)-PC

Reported amino acid change:

C?Y

Comment:

Reported nucleotide numbering from FBrf0048095.

(Harrison et al., 1993)

Variant Molecular Consequences

Associated Sequence Data

DDBJ / EMBL / GenBank

DNA sequence

Protein sequence

UniProtKB/Swiss-Prot

UniProtKB/TrEMBL

Expression Data

Reporter Expression

Additional Information

Statement

Reference

Marker for

Reflects expression of

Reporter construct used in assay

Human Disease Associations

Disease Ontology (DO) Annotations

Models Based on Experimental Evidence ( 0 )

Disease

Evidence

References

Modifiers Based on Experimental Evidence ( 0 )

Disease

Interaction

References

Comments on Models/Modifiers Based on Experimental Evidence ( 0 )

Disease-implicated variant(s)

Phenotypic Data

Phenotypic Class

Phenotype Manifest In

Detailed Description

Statement

Reference

su(Hw)⁷/Df(3R)su(Hw)-A1933 transheterozygous females are fertile but show loss of the gypsy insulator function (assayed through body, wing and bristle phenotypes induced by mutations in the y, ct and f genes).

(Baxley et al., 2017)

P{SUPor-P} induced double strand breakage repair is increased about twofold in a su(Hw)^V/su(Hw)⁷ background compared to wild-type. This phenotype is also seen in flies derived from su(Hw)^V/su(Hw)⁷ parents.

(Lankenau et al., 2000)

Partial suppression of the y² phenotype.

(Harrison et al., 1993)

su(Hw)²/su(Hw)⁷ heterozygotes almost completely suppress the "Hw" phenotype ac^Hw-1+R5, extra macrochaetae are seen on the pleura and postnotum. This was accompanied by a 2--3 fold reduction of ac RNA, sc RNA levels were unchanged. A positive correlation can be seen between increased levels of ac transcripts and the appearance of the "Hw" phenotype.

(Campuzano et al., 1986)

External Data

Linkouts

Interactions

Show genetic interaction network for Enhancers & Suppressors

Phenotypic Class

Enhanced by

Statement

Reference

su(Hw)⁷/su(Hw)^E8, w^BR.BR has abnormal eye color phenotype, enhanceable by Pc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.BR has abnormal eye color phenotype, enhanceable by Scm^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.BR has abnormal eye color phenotype, enhanceable by esc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, y^+mDint2 has abnormal body color phenotype, enhanceable by Pc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has abnormal eye color phenotype, enhanceable by Scm^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has abnormal eye color phenotype, enhanceable by Pc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has abnormal eye color phenotype, enhanceable by esc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, y^+mDint2 has abnormal body color phenotype, enhanceable by Scm^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, y^+mDint2 has abnormal body color phenotype, enhanceable by esc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

NOT Enhanced by

Statement

Reference

su(Hw)⁷/su(Hw)^E8, y^+mDint2 has abnormal body color phenotype, non-enhanceable by Scm^{ZnF-ΔSPM.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.BR has abnormal eye color phenotype, non-enhanceable by esc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.BR has abnormal eye color phenotype, non-enhanceable by Scm^{ZnF-ΔSPM.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has abnormal eye color phenotype, non-enhanceable by esc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has abnormal eye color phenotype, non-enhanceable by Scm^{ZnF-ΔSPM.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, y^+mDint2 has abnormal body color phenotype, non-enhanceable by esc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

Suppressed by

Statement

Reference

Scm^{ZnF.hs.Tag:FLAG}, su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has abnormal eye color phenotype, suppressible by ph-p⁴⁰⁹

(Roseman et al., 2001)

Pc^{ZnF.hs.Tag:FLAG}, su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has abnormal eye color phenotype, suppressible by ph-p⁴⁰⁹

(Roseman et al., 2001)

esc^{ZnF.hs.Tag:FLAG}, su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has abnormal eye color phenotype, suppressible by ph-p⁴⁰⁹

(Roseman et al., 2001)

Enhancer of

Statement

Reference

su(Hw)⁷/su(Hw)^V is an enhancer of visible phenotype of sc⁵

(Golovnin et al., 2003)

Suppressor of

Statement

Reference

su(Hw)⁷/su(Hw)^V is a suppressor of visible phenotype of ap^f00451

(Gohl et al., 2008)

su(Hw)⁷/su(Hw)^V is a suppressor of abnormal body color phenotype of y^eve-700gin

(Lee and Wu, 2006)

su(Hw)⁷/su(Hw)^V is a suppressor of abnormal body color phenotype of y^w-700gin

(Lee and Wu, 2006)

su(Hw)⁷/su(Hw)^V is a suppressor | partially of visible phenotype of sc^ms2

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor | partially of visible phenotype of sc^ms1

(Golovnin et al., 2003)

su(Hw)⁷ is a suppressor of abnormal eye color | recessive phenotype of w^E.BR.BR

(Roseman et al., 1993)

NOT Suppressor of

Statement

Reference

su(Hw)⁷/su(Hw)^V is a non-suppressor of visible phenotype of ap^{P1\loxP.MCP-PRE.MM}

(Gohl et al., 2008)

Other

Statement

Reference

sc⁵, su(Hw)⁷/su(Hw)^V has viable phenotype

(Golovnin et al., 2003)

In(1)sc^V2, su(Hw)⁷/su(Hw)^V has viable phenotype

(Golovnin et al., 2003)

In(1)sc^V2, su(Hw)⁷/su(Hw)^V has visible phenotype

(Golovnin et al., 2003)

In(1)sc^V2, su(Hw)⁷/su(Hw)^V has abnormal body color phenotype

(Golovnin et al., 2003)

Df(1)ase-1, su(Hw)⁷/su(Hw)^V has lethal phenotype

(Golovnin et al., 2003)

In(1)sc⁸, su(Hw)⁷/su(Hw)^V has viable phenotype

(Golovnin et al., 2003)

In(1)sc⁸, su(Hw)⁷/su(Hw)^V has visible phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has viable phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has visible phenotype

(Golovnin et al., 2003)

Phenotype Manifest In

Enhanced by

Statement

Reference

su(Hw)⁷/su(Hw)^E8, w^BR.BR has pigment cell phenotype, enhanceable by Pc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.BR has pigment cell phenotype, enhanceable by Scm^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.BR has pigment cell phenotype, enhanceable by esc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has pigment cell phenotype, enhanceable by Scm^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has pigment cell phenotype, enhanceable by Pc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has pigment cell phenotype, enhanceable by esc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, y^+mDint2 has adult cuticle phenotype, enhanceable by Scm^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, y^+mDint2 has adult cuticle phenotype, enhanceable by esc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

NOT Enhanced by

Statement

Reference

su(Hw)⁷/su(Hw)^E8, w^BR.BR has pigment cell phenotype, non-enhanceable by esc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.BR has pigment cell phenotype, non-enhanceable by Scm^{ZnF-ΔSPM.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has pigment cell phenotype, non-enhanceable by esc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has pigment cell phenotype, non-enhanceable by Scm^{ZnF-ΔSPM.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, y^+mDint2 has adult cuticle phenotype, non-enhanceable by esc^{ZnF.hs.Tag:FLAG}

(Roseman et al., 2001)

su(Hw)⁷/su(Hw)^E8, y^+mDint2 has adult cuticle phenotype, non-enhanceable by Scm^{ZnF-ΔSPM.hs.Tag:FLAG}

(Roseman et al., 2001)

Suppressed by

Statement

Reference

Scm^{ZnF.hs.Tag:FLAG}, su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has pigment cell phenotype, suppressible by ph-p⁴⁰⁹

(Roseman et al., 2001)

Pc^{ZnF.hs.Tag:FLAG}, su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has pigment cell phenotype, suppressible by ph-p⁴⁰⁹

(Roseman et al., 2001)

esc^{ZnF.hs.Tag:FLAG}, su(Hw)⁷/su(Hw)^E8, w^BR.E.BR has pigment cell phenotype, suppressible by ph-p⁴⁰⁹

(Roseman et al., 2001)

Enhancer of

Statement

Reference

su(Hw)⁷/su(Hw)^V is an enhancer of scutellar bristle phenotype of sc⁵

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is an enhancer of scutellar bristle phenotype of sc⁸

(Golovnin et al., 2003)

NOT Enhancer of

Statement

Reference

su(Hw)⁷/su(Hw)^V is a non-enhancer of scutellar bristle phenotype of sc^V2

(Golovnin et al., 2003)

Suppressor of

Statement

Reference

su(Hw)⁷/su(Hw)^V is a suppressor of wing phenotype of ap^f00451

(Gohl et al., 2008)

su(Hw)⁷/su(Hw)^V is a suppressor of anterior notopleural bristle phenotype of sc^ms1

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor | partially of anterior orbital bristle phenotype of sc^ms1

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor of anterior supraalar bristle phenotype of sc^ms1

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor of ocellar bristle phenotype of sc^ms1

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor of postocellar bristle phenotype of sc^ms1

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor of presutural bristle phenotype of sc^ms1

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor of scutellar bristle phenotype of sc^ms1

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor of anterior notopleural bristle phenotype of sc^ms2

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor | partially of anterior orbital bristle phenotype of sc^ms2

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor of anterior supraalar bristle phenotype of sc^ms2

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor of ocellar bristle phenotype of sc^ms2

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor of postocellar bristle phenotype of sc^ms2

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor of presutural bristle phenotype of sc^ms2

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a suppressor of scutellar bristle phenotype of sc^ms2

(Golovnin et al., 2003)

su(Hw)⁷, su(Hw)^V, su(Hw)^Δ706-736 is a suppressor of phenotype of y²

(Kim et al., 1996)

su(Hw)⁷, su(Hw)^V, su(Hw)^Δ853-880 is a suppressor of phenotype of y²

(Kim et al., 1996)

su(Hw)^Δ673-943, su(Hw)⁷, su(Hw)^V is a suppressor of phenotype of y²

(Kim et al., 1996)

su(Hw)⁷, su(Hw)^V, su(Hw)^{Δ2-203.673-943} is a suppressor of phenotype of y²

(Kim et al., 1996)

su(Hw)⁷, su(Hw)^V, su(Hw)^Δ738-780 is a suppressor of phenotype of y²

(Kim et al., 1996)

su(Hw)⁷, su(Hw)^V, su(Hw)^Δ782-944 is a suppressor of phenotype of y²

(Kim et al., 1996)

su(Hw)⁷ is a suppressor of pigment cell phenotype of w^E.BR.BR

(Roseman et al., 1993)

su(Hw)⁷ is a suppressor of phenotype of ct^K

(Hoover et al., 1992)

su(Hw)⁷/su(Hw)[+] is a suppressor of phenotype of ct^MRpN30

(Hoover et al., 1992)

su(Hw)⁷ is a suppressor of phenotype of y^D-786

(Smith and Corces, 1992)

su(Hw)⁷ is a suppressor of phenotype of y^D-CLTR

(Smith and Corces, 1992)

su(Hw)⁷ is a suppressor of phenotype of y^D-CTLR

(Smith and Corces, 1992)

su(Hw)⁷ is a suppressor of wing phenotype of r^sP1

(Zerges et al., 1992)

su(Hw)⁷ is a suppressor of wing phenotype of r^sP2

(Zerges et al., 1992)

NOT Suppressor of

Statement

Reference

su(Hw)⁷/su(Hw)^V is a non-suppressor of wing phenotype of ap^{P1\loxP.MCP-PRE.MM}

(Gohl et al., 2008)

su(Hw)⁷/su(Hw)^V is a non-suppressor of humeral bristle phenotype of sc^ms1

(Golovnin et al., 2003)

su(Hw)⁷/su(Hw)^V is a non-suppressor of humeral bristle phenotype of sc^ms2

(Golovnin et al., 2003)

su(Hw)⁷, su(Hw)^V, su(Hw)^wt is a non-suppressor of phenotype of y²

(Kim et al., 1996)

su(Hw)⁷, su(Hw)^V, su(Hw)^Δ2-203 is a non-suppressor of phenotype of y²

(Kim et al., 1996)

su(Hw)⁷, su(Hw)^Δ656-705, su(Hw)^V is a non-suppressor of phenotype of y²

(Kim et al., 1996)

su(Hw)⁷, su(Hw)^V, su(Hw)^Δ881-944 is a non-suppressor of phenotype of y²

(Kim et al., 1996)

Other

Statement

Reference

sc⁵, su(Hw)⁷/su(Hw)^V has ocellar bristle phenotype

(Golovnin et al., 2003)

sc^V2, su(Hw)⁷/su(Hw)^V has anterior orbital bristle phenotype

(Golovnin et al., 2003)

sc^V2, su(Hw)⁷/su(Hw)^V has presutural bristle phenotype

(Golovnin et al., 2003)

sc^V2, su(Hw)⁷/su(Hw)^V has anterior supraalar bristle phenotype

(Golovnin et al., 2003)

sc^V2, su(Hw)⁷/su(Hw)^V has anterior notopleural bristle phenotype

(Golovnin et al., 2003)

sc^V2, su(Hw)⁷/su(Hw)^V has postocellar bristle phenotype

(Golovnin et al., 2003)

sc⁵, su(Hw)⁷/su(Hw)^V has anterior orbital bristle phenotype

(Golovnin et al., 2003)

sc⁵, su(Hw)⁷/su(Hw)^V has anterior supraalar bristle phenotype

(Golovnin et al., 2003)

In(1)sc^V2, su(Hw)⁷/su(Hw)^V has vertical bristle 1 phenotype

(Golovnin et al., 2003)

In(1)sc^V2, su(Hw)⁷/su(Hw)^V has anterior dorsocentral bristle phenotype

(Golovnin et al., 2003)

In(1)sc^V2, su(Hw)⁷/su(Hw)^V has posterior dorsocentral bristle phenotype

(Golovnin et al., 2003)

In(1)sc^V2, su(Hw)⁷/su(Hw)^V has posterior supraalar bristle phenotype

(Golovnin et al., 2003)

In(1)sc^V2, su(Hw)⁷/su(Hw)^V has mesothoracic tergum & microchaeta phenotype

(Golovnin et al., 2003)

sc⁵, su(Hw)⁷/su(Hw)^V has postocellar bristle phenotype

(Golovnin et al., 2003)

In(1)sc⁸, su(Hw)⁷/su(Hw)^V has vertical bristle 1 phenotype

(Golovnin et al., 2003)

In(1)sc⁸, su(Hw)⁷/su(Hw)^V has anterior dorsocentral bristle phenotype

(Golovnin et al., 2003)

In(1)sc⁸, su(Hw)⁷/su(Hw)^V has posterior dorsocentral bristle phenotype

(Golovnin et al., 2003)

In(1)sc⁸, su(Hw)⁷/su(Hw)^V has posterior supraalar bristle phenotype

(Golovnin et al., 2003)

In(1)sc⁸, su(Hw)⁷/su(Hw)^V has mesothoracic tergum & microchaeta phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has vertical bristle 1 phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has scutellar bristle phenotype

(Golovnin et al., 2003)

sc⁸, su(Hw)⁷/su(Hw)^V has humeral bristle phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has humeral bristle phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has ocellar bristle phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has anterior dorsocentral bristle phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has posterior dorsocentral bristle phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has anterior orbital bristle phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has presutural bristle phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has anterior supraalar bristle phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has anterior notopleural bristle phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has postocellar bristle phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has posterior supraalar bristle phenotype

(Golovnin et al., 2003)

sc⁸, su(Hw)⁷/su(Hw)^V has presutural bristle phenotype

(Golovnin et al., 2003)

In(1)y^3P, su(Hw)⁷/su(Hw)^V has mesothoracic tergum & microchaeta phenotype

(Golovnin et al., 2003)

sc⁸, su(Hw)⁷/su(Hw)^V has anterior supraalar bristle phenotype

(Golovnin et al., 2003)

sc^V2, su(Hw)⁷/su(Hw)^V has humeral bristle phenotype

(Golovnin et al., 2003)

sc^V2, su(Hw)⁷/su(Hw)^V has ocellar bristle phenotype

(Golovnin et al., 2003)

Additional Comments

Genetic Interactions

Statement

Reference

Introduction of su(Hw)^V/su(Hw)⁷ restores viability to bgm^38f-ex animals.

(Berkaeva et al., 2009)

A su(Hw)^V/su(Hw)⁷ background almost completely suppresses the wing defects seen in ap^f00451 mutant flies.

A su(Hw)^V/su(Hw)⁷ mutant background has no effect on the wing defects seen in ap^{loxP.MCP-PRE.MM} mutant flies.

(Gohl et al., 2008)

A su(Hw)^V/su(Hw)⁷ background is unable to suppress the enhancer blocking seen in flies expressing y^62D.DNR. The same light wing blade and body pigmentation is seen as is seen in y^62D.DNR alone.

(Kuhn-Parnell et al., 2008)

w^{Scer\FRT.S.P1\loxP.S} flies carrying su(Hw)^V/su(Hw)⁷ tend to have lighter eye pigmentation than w^{Scer\FRT.S.P1\loxP.S} flies.

w^{P1\loxP.S.dW.Scer\FRT.S} flies carrying su(Hw)^V/su(Hw)⁷ tend to have darker eye pigmentation than w^{P1\loxP.S.dW.Scer\FRT.S} flies.

w^{ΔS.dW.Scer\FRT.S} flies carrying su(Hw)^V/su(Hw)⁷ tend to have lighter eye pigmentation than w^{ΔS.dW.Scer\FRT.S} flies.

(Mel'nik et al., 2004)

Body colour: flies carrying y^{Eye125bpYSW.Scer\FRT.P1\loxP} (in a y^- background) have wild-type levels of pigmentation if they are also carrying su(Hw)^V/su(Hw)⁷. In(1)y^3P ; su(Hw)^V/su(Hw)⁷ animals show loss of a number of bristles. Bristle pigmentation is normal in these animals. In(1)sc^V2 ; su(Hw)^V/su(Hw)⁷ animals show loss of a number of bristles. Bristle pigmentation shows mild variegation in these animals; about half the bristles are yellow. In(1)sc⁸ ; su(Hw)^V/su(Hw)⁷ animals show loss of a number of bristles. Bristle pigmentation is normal in these animals. sc⁵ ; su(Hw)^V/su(Hw)⁷ animals show loss of a number of bristles. Bristle pigmentation is normal in these animals.

(Golovnin et al., 2003)

Pigmentation of y¹/y¹; y^{P1\loxP.su(Hw)BR-y-AS-C.-900} animals is largely unaffected by a su(Hw)⁷/Df(3R)su(Hw)V background.

(Parnell et al., 2003)

In a su(Hw)^V/su(Hw)⁷ background, the adbdominal phenotype of Abd-B^{Fab7-2.gypsy\su(Hw)BR-340}/+ males reverts to that seen in Fab-7² flies.

(Hogga et al., 2001)

su(Hw)²/su(Hw)⁷ heteroallelic combination strongly suppresses gypsy insertions.

(Dorsett, 1993)

su(Hw)^V/su(Hw)⁷ restores wild type coloration to y^-800, y^-800R, y^-1868, y^+660R and y⁺⁶⁶⁰.

(Geyer and Corces, 1992)

Dominant suppressor of ct^K and ct^MRpN30, but suppression is less complete than for su(Hw)^V.

(Hoover et al., 1992)

Heterozygotes with su(Hw)² suppress oblique truncated wing of r^sP1 and r^sP2. Effect on r^sP1 is recessive. Effect on r^sP2 is semidominant. Suppression not temperature-dependent as previously reported (Cramer DIS 55:197 ).

(Zerges et al., 1992)

Xenogenetic Interactions

Statement

Reference

Complementation and Rescue Data

Comments

Neither su(Hw)^A2663 nor su(Hw)^A460 complements su(Hw)⁷, a separation-of-function alleles that only affects the gypsy insulator function (assayed through body, wing and bristle phenotypes induced by mutations in the y, ct and f genes), this allele is complemented by su(Hw)^M393 (a separation-of-function allele that impairs female fertility).

(Baxley et al., 2017)

Images (0)

Mutant

Wild-type

Stocks (0)

Notes on Origin

Discoverer

Grell.

(Lindsley and Zimm, 1992)

Arose on: In(3LR)TM6.

(Lindsley and Zimm, 1992)

External Crossreferences and Linkouts ( 0 )

Synonyms and Secondary IDs (4)

Reported As

Symbol Synonym

M10

(Baxley et al., 2017)

Su(Hw)^f

(Kuhn-Parnell et al., 2008, Soshnev et al., 2008, Mel'nik et al., 2004, Lu et al., 2001)

su(Hw)⁷

su(Hw)^f

(Radion et al., 2019, Baxley et al., 2017, Melnikova et al., 2017, Kahn et al., 2016, Savitsky et al., 2016, Gohl et al., 2011, Krivega et al., 2010, Berkaeva et al., 2009, Gohl et al., 2008, Kuhn-Parnell et al., 2008, Lee and Wu, 2006, Ramos et al., 2006, Golovnin et al., 2005, Golovnin et al., 2003, Parnell et al., 2003, Hogga et al., 2001, Roseman et al., 2001, Wei and Brennan, 2001, Lankenau et al., 2000, Parnell and Geyer, 2000, Scott et al., 1999, Mallin et al., 1998, Sigrist and Pirrotta, 1997, Tsai et al., 1997, Hagstrom et al., 1996, Kim et al., 1996, Cai and Levine, 1995, Gomez-Skarmeta et al., 1995, Roseman et al., 1995, Roseman et al., 1995, Scott and Geyer, 1995, Slusarski et al., 1995, Dorsett, 1993, Harrison et al., 1993, Roseman et al., 1993, Geyer and Corces, 1992, Hoover et al., 1992, Lindsley and Zimm, 1992, Smith and Corces, 1992, Zerges et al., 1992, Holdridge and Dorsett, 1991, Dorsett, 1990, Dorsett et al., 1989, Parkhurst et al., 1988)

Name Synonyms

Secondary FlyBase IDs

References (49)

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