Amino acid replacement: R572H.
Nucleotide substitution: A2583G.
A16143756G
A2583G
H573R | Sb-PA; H573R | Sb-PB
H572R
First difference from wild type evident at around 40 hours of pupal development, when the number of actin filament bundles becomes abruptly reduced, then disorganised at the tip accounting for the resulting frayed bristle ends.
homozygous viable
Sbsbd-201, brunspecified has visible phenotype
Sbsbd-201, zipunspecified has visible phenotype
E(zip)31-631-6, Sbsbd-1/Sbsbd-201 has visible phenotype
RhoGEF204291, Sbsbd-1/Sbsbd-201 has visible phenotype
RhoGEF21.1, Sbsbd-1/Sbsbd-201 has visible phenotype
RhoGEF24.1, Sbsbd-1/Sbsbd-201 has visible phenotype
E(zip)12-5[+]/E(zip)12-512-5, Sbsbd-1/Sbsbd-201 has visible phenotype
E(zip)18-5[+]/E(zip)18-518-5, Sbsbd-1/Sbsbd-201 has visible phenotype
E(zip)31-631-6/E(zip)31-6[+], Sbsbd-1/Sbsbd-201 has visible phenotype
RhoGEF204291/RhoGEF2[+], Sbsbd-1/Sbsbd-201 has visible phenotype
RhoGEF21.1/RhoGEF2[+], Sbsbd-1/Sbsbd-201 has visible phenotype
RhoGEF211-3/RhoGEF2[+], Sbsbd-1/Sbsbd-201 has visible phenotype
RhoGEF24.1/RhoGEF2[+], Sbsbd-1/Sbsbd-201 has visible phenotype
RhoGEF211-3, Sbsbd-1/Sbsbd-201 has visible phenotype
E(zip)12-512-5, Sbsbd-1/Sbsbd-201 has visible phenotype
E(zip)18-518-5, Sbsbd-1/Sbsbd-201 has visible phenotype
Sbsbd-201, brunspecified has leg phenotype
Sbsbd-201, zipunspecified has leg phenotype
E(zip)31-631-6, Sbsbd-1/Sbsbd-201 has leg phenotype
RhoGEF204291, Sbsbd-1/Sbsbd-201 has leg phenotype
RhoGEF21.1, Sbsbd-1/Sbsbd-201 has leg phenotype
RhoGEF24.1, Sbsbd-1/Sbsbd-201 has leg phenotype
E(zip)12-5[+]/E(zip)12-512-5, Sbsbd-1/Sbsbd-201 has leg phenotype
E(zip)18-5[+]/E(zip)18-518-5, Sbsbd-1/Sbsbd-201 has leg phenotype
E(zip)31-631-6/E(zip)31-6[+], Sbsbd-1/Sbsbd-201 has leg phenotype
RhoGEF204291/RhoGEF2[+], Sbsbd-1/Sbsbd-201 has leg phenotype
RhoGEF21.1/RhoGEF2[+], Sbsbd-1/Sbsbd-201 has leg phenotype
RhoGEF211-3/RhoGEF2[+], Sbsbd-1/Sbsbd-201 has leg phenotype
RhoGEF24.1/RhoGEF2[+], Sbsbd-1/Sbsbd-201 has leg phenotype
RhoGEF211-3, Sbsbd-1/Sbsbd-201 has leg phenotype
E(zip)12-512-5, Sbsbd-1/Sbsbd-201 has leg phenotype
E(zip)18-518-5, Sbsbd-1/Sbsbd-201 has leg phenotype
Sbsbd-201 interacts with brunspecified or zipunspecified to produce flies with severely malformed legs.
Pkn06736 shows a weak dominant enhancement of leg malformation in Sbsbd-201/Sbsbd-1 flies. Pkn3 shows a weak dominant enhancement of leg malformation in Sbsbd-201/Sbsbd-1 flies. Sbsbd-201/Sbsbd-1 shows a strong interaction (at least 50% of double mutants have at least one malformed leg) with the following mutations: Rho1J3.8/+, Rho1E3.10/+, Df(2R)Jp8/+, Df(2R)Jp1/+, Rho112-6/+. Sbsbd-201/Sbsbd-1 shows a moderate interaction (25-49% of double mutants have at least one malformed leg) with the following mutations: E(zip)18-518-5/+, E(zip)31-631-6/+, zip33-1/+, RhoGEF211-3/+. Sbsbd-201/Sbsbd-1 shows a weak interaction (5-24% of double mutants have at least one malformed leg) with the following mutations: RhoGEF21.1/+, RhoGEF24.1/+, RhoGEF204291/+, rok1/+, rok2/+ and E(zip)12-512-5/+.
Df(3R)sbd105/Sbsbd-201 is partially rescued by Sbhs.PB
Df(3R)sbd105/Sbsbd-201 is not rescued by SbS737A.hs