FlyBase Allele Report: Dmel\Kr[If-1]

General Information

Symbol

Dmel\Kr^If-1

Species

D. melanogaster

Name

FlyBase ID

FBal0005583

Feature type

allele

Associated gene

Dmel\Kr

Associated Insertion(s)

Carried in Construct

Also Known As

Allele class

neomorphic allele - genetic evidence

Mutagen

spontaneous

Nature of the Allele

Allele class

neomorphic allele - genetic evidence

(Hiebert and Birchler, 1994)

Mutagen

spontaneous

(Ives, 1967)

Mutations Mapped to the Genome

Type

Location

Additional Notes

References

Associated Sequence Data

DDBJ / EMBL / GenBank

DNA sequence

Protein sequence

UniProtKB/Swiss-Prot

UniProtKB/TrEMBL

Progenitor genotype

Cytology

Nature of the lesion

Statement

Reference

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 )

Phenotypic Data

Phenotypic Class

visible

(Gangaraju et al., 2011, Baker et al., 1992)

visible | dominant

(Abrell et al., 2000, Carrera et al., 1998, Bhadra et al., 1997, Hiebert and Birchler, 1994, Ives, 1967)

Phenotype Manifest In

Detailed Description

Statement

Reference

Mutants have an eye outgrowth phenotype. Feeding geldanamycin to homozygous females increases the frequency of the ectopic eye outgrowth phenotype by approximately 10-fold.

(Gangaraju et al., 2011)

Kr^If-1/+ flies have small rough eyes.

(Sollars et al., 2003)

The size of the eye is reduced and the ommatidia ared fused or absent in the ventral part of the eye and irregularly arranged dorsally.

(Abrell et al., 2000)

Heterozygotes have small, narrow eyes that are pointed ventrally. In the ventral portion of the eye the facets are fused or absent and dorsally they are irregularly arranged. Eyes are further reduced in size in homozygotes, forming narrow slits with a glossy surface lacking most ommatidia.

(Carrera et al., 1998)

The number of ommatidia is abnormal in heterozygotes.

(Bhadra et al., 1997)

Displays locomotor activity rhythm with an approximately 24h period.

(Vosshall and Young, 1995)

Kr^If-1 males that are also mutant for mle⁴ show a more severe phenotype than their mle⁴/+ sibs.

(Hiebert and Birchler, 1994)

Kr^If-1 results in a rough eye phenotype which is more extreme in homozygotes. Eye discs are deeply folded and smaller than wild type. Ommatidia begin to form posterior to the morphogenetic furrow but later stages of ommatidial development are more rarely seen. The adult eye is greatly reduced in size and is made up of pigment cells and lacunae. Photoreceptor rhabdomeres are only rarely found, and have unusual morphology. The eye region sometimes differentiates cuticle.

(Baker et al., 1992)

The mutant phenotype of Kr^If-1 is due to a developmental defect in precursor cells. When heterozygous with apx¹ the adult eye is half the normal size, the ventral half more prone to irregularities. Eye disc has a fairly large number of clusters with irregular arrangements. When heterozygous with st adult eye is narrow and ventral half is devoid of facets. Rhabdomeres are fused and only 20 ommatidia are present. Eye disc size is reduced with few clusters.

(Renfranz and Benzer, 1989)

The eye area is reduced to approximately one-half that of wild-type in heterozygotes, it is oblong and generally pointed ventrally. The facets are irregularly distributed, are frequently missing across the middle of the eye, and are sometimes fused or absent in the ventral portion. The eye is a narrow slit in homozygotes and has a smooth glossy surface. Viability and fecundity of both hetero- and homozygotes is good to excellent.

(Ives, 1967)

In heterozygote, eye area about one-half normal; narrow and pointed ventrally; facets irregular and often missing across middle of eyes, sometimes fused or absent in ventral portion. In homozygote, eyes are narrow slits with smooth glossy surface. In the eye disk of late third instar larvae, fairly large number of cell clusters in irregular arrangement, especially in ventral half of disk (Renfranz and Benzer, 1989). Viability and fertility good. RK1.

External Data

Linkouts

Interactions

Show genetic interaction network for Enhancers & Suppressors

Phenotypic Class

Enhanced by

Statement

Reference

Kr^If-1 has visible phenotype, enhanceable by piwi[+]/piwi¹

(Gangaraju et al., 2011)

Kr^If-1 has visible phenotype, enhanceable by piwi[+]/piwi²

(Gangaraju et al., 2011)

Kr^If-1 has visible phenotype, enhanceable by Hop[+]/Stip1^k00616

(Gangaraju et al., 2011)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(2L)E55

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(2R)Px2

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(2R)bw-S46

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(2R)bw5

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(2R)cn9

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by GstS1⁰⁴²²⁷

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by In(2LR)Px⁴

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(2R)pk78s

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by Kr-h1¹⁰⁶⁴²

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by Mi-2¹

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by Rab6⁰⁸³²³

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(2L)Prl

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by S⁰⁵⁶⁷¹

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by S⁰⁷⁰⁵⁶

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by Sema2a⁰³⁰²¹

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by crol¹⁰⁶³⁹

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by dpp¹⁰⁶³⁸

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by ex⁰¹²⁷⁰

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by ex⁰²²⁷⁸

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by CCT8⁰³⁹⁹⁶

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by chinmo⁰⁴¹¹¹

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by l(2)04548⁰⁴⁵⁴⁸

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(2R)PC4

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by l(2)08492⁰⁸⁴⁹²

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by osa⁰⁰⁰⁹⁰

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by sty^Δ5

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, enhanceable by Mi-2¹/Mi-2[+]

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by osa⁰⁰⁰⁹⁰/osa[+]

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by Fer2LCH[+]/Fer2LCH⁰⁷⁰¹⁶

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(3L)brm11

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(3R)P115

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(3R)kar-D3

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(3R)GB104

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(3R)p712

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(3L)R-G7

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(3L)fz-GF3b

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(3L)W10

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(3L)W4

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by Df(3L)kto2

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, enhanceable by osa[+]/osa⁰⁴⁵³⁹

(Carrera et al., 1998)

Suppressed by

Statement

Reference

Kr^If-1 has visible | dominant phenotype, suppressible by Df(2R)trix

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, suppressible by Sc2⁰⁵⁶³⁴

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, suppressible by Vha55^j2E9

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, suppressible by bun⁰⁵⁴⁷⁹

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, suppressible by bun⁰⁶⁴⁷⁵

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, suppressible by caps⁰²⁹³⁷

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, suppressible by emc⁰⁵⁵⁹²

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, suppressible by sty^L1

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, suppressible by bun⁰²⁶⁸⁷

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, suppressible by Eip75B⁰⁷⁰⁴¹

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, suppressible by In(2L)05887

(Abrell et al., 2000)

Kr^If-1 has visible | dominant phenotype, suppressible by Df(3L)Ar12-1

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by Df(3L)Ar14-8

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by Df(3L)GN19

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by Df(3L)M21

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by Df(3L)HR119

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by Df(3L)AC1

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by Df(3L)Ly

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by Df(3L)H99

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by Df(3R)M-Kx1

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by l(3)06240[+]/Psa⁰⁶²⁴⁰

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by l(3)05967[+]/l(3)05967⁰⁵⁹⁶⁷

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by l(3)neo3[+]/l(3)neo3¹

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by emc[+]/emc⁰⁵⁵⁹²

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by Sc2[+]/Sc2⁰⁵⁶³⁴

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by Sap130⁰⁶⁹²⁴/l(3)06924[+]

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by caps⁰²⁹³⁷/caps[+]

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by Eip75B[+]/Eip75B⁰⁷⁰⁴¹

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by rept[+]/rept⁰⁶⁹⁴⁵

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by Vha55^j2E9/Vha55[+]

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by l(3)j2C3[+]/l(3)j2C3^j2C3

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by l(3)neo39¹/l(3)neo39[+]

(Carrera et al., 1998)

Kr^If-1 has visible | dominant phenotype, suppressible by l(3)neo47[+]/l(3)neo47¹

(Carrera et al., 1998)

Phenotype Manifest In

Enhanced by

Statement

Reference

Kr^If-1 has eye phenotype, enhanceable by piwi[+]/piwi¹

(Gangaraju et al., 2011)

Kr^If-1 has eye phenotype, enhanceable by piwi[+]/piwi²

(Gangaraju et al., 2011)

Kr^If-1 has eye phenotype, enhanceable by Hop[+]/Stip1^k00616

(Gangaraju et al., 2011)

Kr^If-1 has eye phenotype, enhanceable by Df(2R)Px2

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by Df(2R)Px2

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by Df(2R)bw-S46

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by Df(2R)bw-S46

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by Df(2R)bw5

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by Df(2R)bw5

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by Df(2L)E55

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by Df(2R)cn9

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by Df(2R)cn9

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by GstS1⁰⁴²²⁷

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by GstS1⁰⁴²²⁷

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by In(2LR)Px⁴

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by In(2LR)Px⁴

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by Df(2R)pk78s

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by Df(2L)E55

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by Df(2R)pk78s

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by Kr-h1¹⁰⁶⁴²

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by Kr-h1¹⁰⁶⁴²

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by Mi-2¹

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by Mi-2¹

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by Rab6⁰⁸³²³

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by Rab6⁰⁸³²³

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by S⁰⁵⁶⁷¹

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by S⁰⁵⁶⁷¹

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by S⁰⁷⁰⁵⁶

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by S⁰⁷⁰⁵⁶

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by Sema2a⁰³⁰²¹

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by Sema2a⁰³⁰²¹

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by Df(2L)Prl

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by crol¹⁰⁶³⁹

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by crol¹⁰⁶³⁹

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by dpp¹⁰⁶³⁸

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by dpp¹⁰⁶³⁸

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by ex⁰¹²⁷⁰

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by ex⁰¹²⁷⁰

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by ex⁰²²⁷⁸

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by Df(2L)Prl

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by ex⁰²²⁷⁸

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by CCT8⁰³⁹⁹⁶

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by CCT8⁰³⁹⁹⁶

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by chinmo⁰⁴¹¹¹

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by chinmo⁰⁴¹¹¹

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by l(2)04548⁰⁴⁵⁴⁸

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by l(2)04548⁰⁴⁵⁴⁸

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by l(2)08492⁰⁸⁴⁹²

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by l(2)08492⁰⁸⁴⁹²

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by osa⁰⁰⁰⁹⁰

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by osa⁰⁰⁰⁹⁰

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by sty^Δ5

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by sty^Δ5

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by Df(2R)PC4

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, enhanceable by Df(2R)PC4

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, enhanceable by osa[+]/osa⁰⁴⁵³⁹

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by Mi-2¹/Mi-2[+]

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by osa⁰⁰⁰⁹⁰/osa[+]

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by Fer2LCH[+]/Fer2LCH⁰⁷⁰¹⁶

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by Df(3L)brm11

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by Df(3R)P115

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by Df(3R)kar-D3

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by Df(3R)GB104

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by Df(3R)p712

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by Df(3L)R-G7

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by Df(3L)fz-GF3b

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by Df(3L)W10

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by Df(3L)W4

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, enhanceable by Df(3L)kto2

(Carrera et al., 1998)

NOT Enhanced by

Statement

Reference

Kr^If-1 has eye phenotype, non-enhanceable by Low¹

(Bhadra et al., 1997)

Suppressed by

Statement

Reference

Kr^If-1 has eye phenotype, suppressible by Sc2⁰⁵⁶³⁴

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, suppressible by Sc2⁰⁵⁶³⁴

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, suppressible by Vha55^j2E9

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, suppressible by Vha55^j2E9

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, suppressible by bun⁰⁵⁴⁷⁹

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, suppressible by bun⁰⁵⁴⁷⁹

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, suppressible by Df(2R)trix

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, suppressible by bun⁰⁶⁴⁷⁵

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, suppressible by bun⁰⁶⁴⁷⁵

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, suppressible by caps⁰²⁹³⁷

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, suppressible by caps⁰²⁹³⁷

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, suppressible by emc⁰⁵⁵⁹²

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, suppressible by emc⁰⁵⁵⁹²

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, suppressible by sty^L1

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, suppressible by Df(2R)trix

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, suppressible by sty^L1

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, suppressible by bun⁰²⁶⁸⁷

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, suppressible by bun⁰²⁶⁸⁷

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, suppressible by Eip75B⁰⁷⁰⁴¹

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, suppressible by Eip75B⁰⁷⁰⁴¹

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, suppressible by In(2L)05887

(Abrell et al., 2000)

Kr^If-1 has ommatidium phenotype, suppressible by In(2L)05887

(Abrell et al., 2000)

Kr^If-1 has eye phenotype, suppressible by Df(3L)Ar12-1

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by Df(3L)Ar14-8

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by Df(3L)GN19

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by Df(3L)M21

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by Df(3L)HR119

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by Df(3L)AC1

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by Df(3L)Ly

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by Df(3L)H99

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by Df(3R)M-Kx1

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by l(3)06240[+]/Psa⁰⁶²⁴⁰

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by l(3)05967[+]/l(3)05967⁰⁵⁹⁶⁷

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by l(3)neo3[+]/l(3)neo3¹

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by emc[+]/emc⁰⁵⁵⁹²

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by Sc2[+]/Sc2⁰⁵⁶³⁴

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by Sap130⁰⁶⁹²⁴/l(3)06924[+]

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by caps⁰²⁹³⁷/caps[+]

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by Eip75B[+]/Eip75B⁰⁷⁰⁴¹

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by rept[+]/rept⁰⁶⁹⁴⁵

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by Vha55^j2E9/Vha55[+]

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by l(3)j2C3[+]/l(3)j2C3^j2C3

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by l(3)neo39¹/l(3)neo39[+]

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by l(3)neo47[+]/l(3)neo47¹

(Carrera et al., 1998)

Kr^If-1 has eye phenotype, suppressible by exba[+]/kra⁰³⁰²²

(Carrera et al., 1998)

NOT suppressed by

Statement

Reference

Kr^If-1 has eye phenotype, non-suppressible by Low¹

(Bhadra et al., 1997)

Enhancer of

Statement

Reference

Kr^If-1/Kr[+] is an enhancer of eye phenotype of Scer\GAL4^GMR.PF, fru^NP0021

(Goto et al., 2011)

Other

Statement

Reference

Kr^If-1, fs(1)h¹ has eye phenotype

(Sollars et al., 2003)

Kr^If-1, vtd³ has eye phenotype

(Sollars et al., 2003)

Kr^If-1, kto[+]/kto¹ has eye phenotype

(Sollars et al., 2003)

Kr^If-1, osa²/osa[+] has eye phenotype

(Sollars et al., 2003)

Kr^If-1, skd²/skd[+] has eye phenotype

(Sollars et al., 2003)

Kr^If-1, Nsf2^urd-2/urd[+] has eye phenotype

(Sollars et al., 2003)

Kr^If-1, vtd[+]/vtd³ has eye phenotype

(Sollars et al., 2003)

Kr^If-1, z[+]/z^v77h has eye phenotype

(Sollars et al., 2003)

Hsp83^e4A/Hsp83[+], Kr^If-1 has eye phenotype

(Sollars et al., 2003)

Hsp83^e6A, Kr^If-1 has eye phenotype

(Sollars et al., 2003)

Kr^If-1, Nsf2^urd-2 has eye phenotype

(Sollars et al., 2003)

Kr^If-1, skd² has eye phenotype

(Sollars et al., 2003)

Kr^If-1, osa² has eye phenotype

(Sollars et al., 2003)

Hsp83^e6D, Kr^If-1 has eye phenotype

(Sollars et al., 2003)

Kr^If-1, brm² has eye phenotype

(Sollars et al., 2003)

Kr^If-1, kto¹ has eye phenotype

(Sollars et al., 2003)

Kr^If-1, z^v77h has eye phenotype

(Sollars et al., 2003)

Kr^If-1, btl^dev2 has eye phenotype

(Sollars et al., 2003)

Hsp83^e4A, Kr^If-1 has eye phenotype

(Sollars et al., 2003)

Kr^If-1, Trl^R85 has eye phenotype

(Sollars et al., 2003)

Hsp83[+]/Hsp83^e6A, Kr^If-1 has eye phenotype

(Sollars et al., 2003)

Hsp83^e6D/Hsp83[+], Kr^If-1 has eye phenotype

(Sollars et al., 2003)

Kr^If-1, Trl[+]/Trl^R85 has eye phenotype

(Sollars et al., 2003)

Kr^If-1, brm[+]/brm² has eye phenotype

(Sollars et al., 2003)

Kr^If-1, btl^dev2/btl[+] has eye phenotype

(Sollars et al., 2003)

Kr^If-1, fs(1)h¹/fs(1)h[+] has eye phenotype

(Sollars et al., 2003)

Additional Comments

Genetic Interactions

Statement

Reference

piwi¹/+ and piwi²/+ enhance the eye outgrowth phenotype phenotype of Kr^If-1; approximately 7% of the progeny have an eye outgrowth phenotype in a cross of piwi¹/+ or piwi²/+ females to Kr^If-1/+ males. However, the reciprocal cross of Kr^If-1/+ females to piwi¹/+ or piwi²/+ males does not result in progeny with an eye outgrowth phenotype, indicating a maternal effect. In addition, the expression of the eye outgrowth phenotype depends on the presence of the piwi² mutation in the progeny, indicating a zygotic effect. The ability of geldanamycin to increase the frequency of the ectopic eye outgrowth phenotype in Kr^If-1 homozygous females is reduced if the females are also carrying piwi^5'T:Hsap\MYC. Maternal Hop^k00616 is a dominant enhancer of the eye outgrowth phenotype phenotype of Kr^If-1.

(Gangaraju et al., 2011)

A Kr^If-1 background strongly enhances the rough eye phenotype found upon expression of fru^NP0021 under the control of Scer\GAL4^GMR.PF.

(Goto et al., 2011)

15+/-4% of Kr^If-1/+ flies born to Hsp83^e1D/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 11+/-3% of Kr^If-1/+ flies born to Hsp83^e3A/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 6+/-2% of Kr^If-1/+ flies born to Hsp83^e4A/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 6+/-2% of Kr^If-1/+ flies born to Hsp83^e6A/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 13+/-4% of Kr^If-1/+ flies born to Hsp83^e6D/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 5+/-1% of Kr^If-1/+ flies born to brm²/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 10+/-2% of Kr^If-1/+ flies born to fs(1)h¹/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 15+/-4% of Kr^If-1/+ flies born to kto¹/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 10+/-2% of Kr^If-1/+ flies born to osa²/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 2+/-1% of Kr^If-1/+ flies born to skd²/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 5+/-2% of Kr^If-1/+ flies born to urd²/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 55+/-8% of Kr^If-1/+ flies born to vtd³/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 5+/-2% of Kr^If-1/+ flies born to z^v77h/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 10+/-3% of Kr^If-1/+ flies born to btl^dev2/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers. 10+/-2% of Kr^If-1/+ flies born to Trl^R85/+ mothers have outgrowths with ectopic vibrissae protruding from the ventral region of the eye, compared to less than 0.1% of Kr^If-1/+ flies born to isogenised wild-type mothers.

(Sollars et al., 2003)

Kr^If-1, ex⁰¹²⁷⁰ flies develop smaller eyes and fewer ommatidia than Kr^If-1 flies. Kr^If-1, S⁰⁵⁶⁷¹ eyes show a severe enhancement of the Kr^If-1 phenotype; the eyes only have only remnants of a few ommatidia.

(Abrell et al., 2000)

The eye phenotype is unaffected by Low¹.

(Bhadra et al., 1997)

Xenogenetic Interactions

Statement

Reference

Complementation and Rescue Data

Complements

Kr^unspecified

(Carrera et al., 1998)

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