Allele Dmel\Kr^If-1

General Information
Symbol	Dmel\Kr^If-1	Species	D. melanogaster
Name		FlyBase ID	FBal0005583
Feature type	allele	Created / Updated	2006-08-22/2006-08-22
Associated gene	Dmel\Kr

Allele class	neomorph
Mutagen	spontaneous
Nature of the Allele
Allele class	neomorph (Hiebert and Birchler, 1994)
Mutagen	spontaneous (Ives, 1967)
Mapped Features and Mutations
Type Symbol & Location Additional Notes References
Associated Sequence Data
DDBJ / EMBL / GenBank	DNA sequence Protein sequence Name

UniProtKB/Swiss-Prot
UniProtKB/TrEMBL

Progenitor genotype
Nature of the lesion	Statement Reference
Assay mode
Cytology
Phenotypic Data
Phenotypic Class
	visible (Baker et al., 1992) visible \| dominant (Bhadra et al., 1997, Abrell et al., 2000, Hiebert and Birchler, 1994, Ives, 1967, Carrera et al., 1998)
Phenotype Manifest In
	eye (Bhadra et al., 1997, Sollars et al., 2003, Baker et al., 1992, Abrell et al., 2000, Hiebert and Birchler, 1994, Ives, 1967, Carrera et al., 1998) ommatidium (Bhadra et al., 1997, Baker et al., 1992, Abrell et al., 2000, Carrera et al., 1998) eye disc (Baker et al., 1992) rhabdomere (Baker et al., 1992) adult cuticle \| ectopic (Baker et al., 1992)
Detailed Description
	Statement Reference 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. 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) 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 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) Kr^If-1 males that are also mutant for mle⁴ show a more severe phenotype than their mle⁴/+ sibs. (Hiebert and Birchler, 1994) Displays locomotor activity rhythm with an approximately 24h period. (Vosshall and Young, 1995) The number of ommatidia is abnormal in heterozygotes. (Bhadra et al., 1997) 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 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) Kr^If-1/+ flies have small rough eyes. (Sollars et al., 2003)
Interactions
	Show the genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
Statement Reference 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(2L)Prl (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 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 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 Sema-2a⁰³⁰²¹ (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 l(2)03996⁰³⁹⁹⁶ (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 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 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) 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)
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 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 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 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[+]/l(3)06240⁰⁶²⁴⁰ (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 l(3)06924⁰⁶⁹²⁴/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 Df(2L)E55 (Abrell et al., 2000) Kr^If-1 has ommatidium phenotype, enhanceable by Df(2L)E55 (Abrell et al., 2000) Kr^If-1 has eye phenotype, enhanceable by Df(2L)Prl (Abrell et al., 2000) Kr^If-1 has ommatidium phenotype, enhanceable by Df(2L)Prl (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 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(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(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 Sema-2a⁰³⁰²¹ (Abrell et al., 2000) Kr^If-1 has ommatidium phenotype, enhanceable by Sema-2a⁰³⁰²¹ (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 ex⁰²²⁷⁸ (Abrell et al., 2000) Kr^If-1 has eye phenotype, enhanceable by l(2)03996⁰³⁹⁹⁶ (Abrell et al., 2000) Kr^If-1 has ommatidium phenotype, enhanceable by l(2)03996⁰³⁹⁹⁶ (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(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) 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)
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 Df(2R)trix (Abrell et al., 2000) Kr^If-1 has ommatidium phenotype, suppressible by Df(2R)trix (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 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 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 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 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[+]/l(3)06240⁰⁶²⁴⁰ (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 l(3)06924⁰⁶⁹²⁴/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[+]/exba⁰³⁰²² (Carrera et al., 1998)
NOT suppressed by
Statement Reference Kr^If-1 has eye phenotype, non-suppressible by Low¹ (Bhadra et al., 1997)
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, osa² 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) 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, urd²/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, urd² has eye phenotype (Sollars et al., 2003) Kr^If-1, skd² 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)
Additional Comments
Genetic Interactions
Statement Reference The eye phenotype is unaffected by Low¹. (Bhadra et al., 1997) 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) 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.

Allele Dmel\KrIf-1

Allele Dmel\Kr^If-1