filamentous actin & nurse cell | germ-line clone
filamentous actin & oocyte | germ-line clone
plasma membrane & oocyte | germ-line clone
Females carrying rok2 germline clones (GLCs) produce eggs that are small in 58% of cases and exhibit fused dorsal appendages in 100% of cases. Oocytes within these clones exhibit actin clumps in the ooplasm (75% penetrance) and an altered plasma membrane (62% penetrance). Additionally, the F-actin network is perturbed in nurse cells in 72% of rok1 GLCs.
rok[+]/Rok1 is a non-enhancer of visible phenotype of Scer\GAL4en-e16E, kermitGS2053
Rok[+]/Rok1 is a suppressor | partially of decreased size | adult stage phenotype of Scer\GAL4A9, ShrmA.UAS
Rok[+]/Rok1 is a suppressor | partially of visible | adult stage phenotype of Scer\GAL4A9, ShrmA.UAS
Rok1 is a suppressor of visible phenotype of HUAS.cMa, Scer\GAL4GMR.PF
rok[+]/Rok1 is a suppressor of visible phenotype of LIMK1UAS.cCa, Scer\GAL4en-e16E
Rok1 is a suppressor of abnormal cell polarity phenotype of pkpk.sev
Rok1 is a suppressor of lethal | recessive | larval stage phenotype of MoeG0323
rok[+]/Rok1 is a non-suppressor of visible phenotype of Scer\GAL4en-e16E, kermitGS2053
Rok1, sqhEE.EGFP has abnormal cell migration phenotype
Df(3R)sbd105/+, Rok1 has visible | dominant phenotype
Rho1E3.10/Rho1[+], Rok1 has partially lethal phenotype
Rok[+]/Rok1 is an enhancer of wing hair | increased number phenotype of Scer\GAL4en.PU, cmbUAS.RA.Tag:FLAG
rok[+]/Rok1 is a non-enhancer of wing hair phenotype of Scer\GAL4en-e16E, kermitGS2053
Rok[+]/Rok1 is a suppressor | partially of wing phenotype of Scer\GAL4A9, ShrmA.UAS
Rok1 is a suppressor of eye phenotype of HUAS.cMa, Scer\GAL4GMR.PF
rok[+]/Rok1 is a suppressor of wing phenotype of LIMK1UAS.cCa, Scer\GAL4en-e16E
Rok1 is a suppressor of ommatidium phenotype of pkpk.sev
rok[+]/Rok1 is a non-suppressor of wing hair phenotype of Scer\GAL4en-e16E, kermitGS2053
Heterozygosity significantly enhances the multiple hair cell phenotype of Scer\GAL4en.PU cmbScer\UAS.RA wings.
Embryos expressing sqhEE.T:Avic\GFP-EGFP in a Rok1 mutant background fail to undergo mesoderm invagination.
rok1/+ suppresses the mutant wing phenotype caused by expression of LIMK1Scer\UAS.cCa under the control of Scer\GAL4en-e16E (the % of wings with normal morphology at 18oC is increased from 9% to 64%). The frequency of the malformed leg phenotype seen in Sb63b/+ heterozygotes (8%) is increased if the flies are also heterozygous for rok1 (24%). The frequency of the malformed leg phenotype seen in Sb70/+ heterozygotes (7%) is increased if the flies are also heterozygous for rok1 (94%).
rok1 shows a strong interaction (at least 50% of double heterozygotes have at least one malformed leg) with the following mutations: Sb70. rok1 shows a weak interaction (5-24% of double heterozygotes have at least one malformed leg) with the following mutations: Sb63b, Df(3R)sbd105 and Rho112-6. rok1 shows a strong interaction (at least 50% of double heterozygotes have at least one malformed wing) with the following mutations: Rho1E3.10 and zipEbr. rok1 shows a moderate interaction (25-49% of double heterozygotes have at least one malformed wing) with the following mutations: Sb70. rok1 shows a weak interaction (5-24% of double heterozygotes have at least one malformed wing) with the following mutations: Sb63b. Sbsbd-201/Sbsbd-1 shows a weak interaction (5-24% of double mutants have at least one malformed leg) with the following mutations: rok1/+.