Rho1J3.8, RhoGEF211-3/RhoGEF2[+] has visible phenotype
RhoGEF211-3/RhoGEF2[+], Sb63b has visible | dominant phenotype
RhoGEF211-3/RhoGEF2[+], Sb63b has visible phenotype
RhoGEF211-3/RhoGEF2[+], Sb70 has visible | dominant phenotype
RhoGEF211-3/RhoGEF2[+], Sb70 has visible phenotype
RhoGEF211-3/RhoGEF2[+], zipEbr has visible phenotype
RhoGEF211-3/RhoGEF2[+], Sbsbd-1/Sbsbd-201 has visible phenotype
Df(2R)Jp8/+, RhoGEF211-3 has visible | dominant phenotype
Df(2R)Jp8/+, RhoGEF211-3 has partially lethal phenotype
Rho1E3.10/Rho1[+], RhoGEF211-3 has visible | dominant phenotype
Rho1E3.10/Rho1[+], RhoGEF211-3 has partially lethal phenotype
Rho1J3.8/Rho1[+], RhoGEF211-3 has visible | dominant phenotype
Rho1J3.8/Rho1[+], RhoGEF211-3 has partially lethal phenotype
E(zip)12-5[+]/E(zip)12-512-5, RhoGEF211-3 has visible | dominant phenotype
E(zip)12-5[+]/E(zip)12-512-5, RhoGEF211-3 has visible phenotype
E(zip)18-5[+]/E(zip)18-518-5, RhoGEF211-3 has visible | dominant phenotype
Rho112-6/Rho1[+], RhoGEF211-3 has visible | dominant phenotype
RhoGEF211-3, Sb63b/Sb[+] has visible | dominant phenotype
RhoGEF211-3, Sb63b/Sb[+] has visible phenotype
RhoGEF211-3, Sb[+]/Sb70 has visible | dominant phenotype
RhoGEF211-3, Sb[+]/Sb70 has visible phenotype
RhoGEF211-3, zip[+]/zipEbr has visible | dominant phenotype
RhoGEF211-3, Sbsbd-1/Sbsbd-201 has visible phenotype
Rho1E3.10, RhoGEF211-3/RhoGEF2[+] has visible phenotype
Rho112-6, RhoGEF211-3/RhoGEF2[+] has visible phenotype
E(zip)12-512-5, RhoGEF211-3/RhoGEF2[+] has visible | dominant phenotype
E(zip)12-512-5, RhoGEF211-3/RhoGEF2[+] has visible phenotype
E(zip)18-518-5, RhoGEF211-3/RhoGEF2[+] has visible phenotype
E(br)444Ebr444, RhoGEF211-3/RhoGEF2[+] has visible | dominant phenotype
E(br)65Ebr65, RhoGEF211-3/RhoGEF2[+] has visible | dominant phenotype
E(br)444[+]/E(br)444Ebr444, RhoGEF211-3 has visible phenotype
E(br)65Ebr65/E(br)65[+], RhoGEF211-3 has visible phenotype
Rho1Ebr233/Rho1[+], RhoGEF211-3 has visible phenotype
Rho1[+]/Rho1Ebr246, RhoGEF211-3 has visible phenotype
Rho1Ebr233, RhoGEF211-3/RhoGEF2[+] has visible | dominant phenotype
Rho1Ebr246, RhoGEF211-3/RhoGEF2[+] has visible | dominant phenotype
Rho1J3.8, RhoGEF211-3 has wing phenotype
Rho1J3.8, RhoGEF211-3 has leg phenotype
RhoGEF211-3/RhoGEF2[+], Sb63b has leg phenotype
RhoGEF211-3, Sb63b has wing phenotype
RhoGEF211-3, Sb63b has leg phenotype
RhoGEF211-3, Sb70 has wing phenotype
RhoGEF211-3, Sb70 has leg phenotype
RhoGEF211-3/RhoGEF2[+], Sb70 has leg phenotype
RhoGEF211-3, zipEbr has wing phenotype
RhoGEF211-3, zipEbr has leg phenotype
RhoGEF211-3/RhoGEF2[+], Sbsbd-1/Sbsbd-201 has leg phenotype
Df(2R)Jp8/+, RhoGEF211-3 has leg phenotype
Rho1E3.10/Rho1[+], RhoGEF211-3 has wing phenotype
Rho1E3.10/Rho1[+], RhoGEF211-3 has leg phenotype
Rho1J3.8/Rho1[+], RhoGEF211-3 has wing phenotype
Rho1J3.8/Rho1[+], RhoGEF211-3 has leg phenotype
Rho1E3.10, RhoGEF211-3 has wing phenotype
E(zip)12-5[+]/E(zip)12-512-5, RhoGEF211-3 has leg phenotype
E(zip)18-5[+]/E(zip)18-518-5, RhoGEF211-3 has leg phenotype
Rho112-6/Rho1[+], RhoGEF211-3 has leg phenotype
RhoGEF211-3, Sb63b/Sb[+] has wing phenotype
Rho1E3.10, RhoGEF211-3 has leg phenotype
RhoGEF211-3, Sb63b/Sb[+] has leg phenotype
RhoGEF211-3, Sb[+]/Sb70 has wing phenotype
RhoGEF211-3, Sb[+]/Sb70 has leg phenotype
RhoGEF211-3, zip[+]/zipEbr has wing phenotype
RhoGEF211-3, zip[+]/zipEbr has leg phenotype
RhoGEF211-3, Sbsbd-1/Sbsbd-201 has leg phenotype
E(zip)12-512-5, RhoGEF211-3 has leg phenotype
Rho112-6, RhoGEF211-3 has leg phenotype
E(zip)12-512-5, RhoGEF211-3/RhoGEF2[+] has leg phenotype
E(zip)18-518-5, RhoGEF211-3 has leg phenotype
E(br)444Ebr444, RhoGEF211-3/RhoGEF2[+] has leg phenotype
Rho1Ebr246, RhoGEF211-3/RhoGEF2[+] has leg phenotype
E(br)65Ebr65, RhoGEF211-3/RhoGEF2[+] has leg phenotype
E(br)444Ebr444, RhoGEF211-3 has leg phenotype
E(br)65Ebr65, RhoGEF211-3 has leg phenotype
Rho1Ebr233, RhoGEF211-3 has leg phenotype
Rho1Ebr246, RhoGEF211-3 has leg phenotype
Rho1Ebr233, RhoGEF211-3/RhoGEF2[+] has leg phenotype
RhoGEF211-3 shows a strong interaction (at least 50% of double heterozygotes have at least one malformed leg) with the following mutations: zipEbr, Rho1J3.8, Df(2R)Jp8, Rho112-6 and Rho1E3.10. RhoGEF211-3 shows a moderate interaction (25-49% of double heterozygotes have at least one malformed leg) with the following mutations: Sb63b, Sb70 and E(zip)12-512-5. RhoGEF211-3 shows a weak interaction (5-24% of double heterozygotes have at least one malformed leg) with the following mutations: E(zip)18-518-5. br1 fails to show a significant genetic interaction (assayed in terms of a malformed leg phenotype) with RhoGEF211-3. RhoGEF211-3 shows a strong interaction (at least 50% of double heterozygotes have at least one malformed wing) with the following mutations: Rho1E3.10, Rho1J3.8, zipEbr and Sb63b. RhoGEF211-3 shows a moderate interaction (25-49% of double heterozygotes have at least one malformed wing) with the following mutations: Sb70. Sbsbd-201/Sbsbd-1 shows a moderate interaction (25-49% of double mutants have at least one malformed leg) with the following mutations: RhoGEF211-3/+.
The fraction of flies showing a malformed leg phenotype in at least one leg, for RhoGEF211-3 in double heterozygous combination with one of the following alleles is - SbEbr20 : 3%, SbEbr48 : 3%, SbEbr228 : 2%, SbEbr448 : 4%, SbEbr536 : 2%, SbEbr623 : 0%, Rho1Ebr233 : 62%, Rho1Ebr246 : 63%, bsEbr292 : 0%, E(br)24Ebr24 : 5%, E(br)65Ebr65 : 28%, E(br)155Ebr155 : 1%, E(br)165Ebr165 : 1%, E(br)333Ebr333 : 3%, E(br)72Ebr72 : 3%, E(br)121Ebr121 : 0%, E(br)160Ebr160 : 4%, E(br)187Ebr187 : 1%, E(br)420Ebr420 : 6% and E(br)444Ebr444 : 44%.