Nonsense mutation at codon 353 predicted to result in a C-terminal truncation of 24 amino acids.
Point mutation.
C1120676T
R353term | rl-PC; R353term | rl-PD; R353term | rl-PE; R308term | rl-PG; R243term | rl-PH
?353term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Mutants have a have a mild rough eye phenotype.
rl9 is a non-enhancer of visible phenotype of RalaS25N.UAS, Scer\GAL4sca-537.4
rl9 is a non-suppressor of visible phenotype of RalaS25N.UAS, Scer\GAL4sca-537.4
rl[+]/rl9 is an enhancer of embryo | posterior phenotype of Dsor1Su1, fs(1)M31901
rl[+]/rl9 is an enhancer of embryonic abdominal segment 8 phenotype of Dsor1Su1, fs(1)M31901
Embryos derived from homozygous fs(1)M31901 females fail to develop structures posterior to the seventh abdominal segment as well as anterior-most structures, including the head skeleton. The posterior defect is significantly suppressed if the female is also carrying one copy of Dsor1Su1; an eighth abdominal segment is formed. This suppression is significantly reduced if the females are also carrying one copy of rl9.
Larval lethality rescued by rlhs.PB construct.
Hilliker.
Phenotypes of rl mutants fall into an allelic series: Df(2R)rl10a/rl1 >= rl9/rl1 > rlla8/rl1 > rl10/rl1 > rl1/rl1.