Reported as an AG to AA mutation in the splice acceptor of the third intron of Hn. Position of mutation on reference sequence inferred by FlyBase curator.
Multiple deletions within the first intron, plus a G to A mutation at the splice acceptor site in the third intron.
eye color defective
RK3 as dominant, RK1 as recessive.
Present in most if not all TM6 chromosomes.
Associated with: In(3LR)TM6.