rdx6 encodes a splice junction mutation (an A to G change in the 23rd nucleotide of the intron between exons 12 and 13).
Nucleotide substitution: A?G.
Homozygous rdx6 embryos fail to hatch.
Embryos derived from rdx6 germline clones (lacking both maternal and zygotic rdx) display a spectrum of developmental defects, ranging from normal patterning (2%), through to a complete failure of cellularization (75%). An intermediate class (23%) includes errors in segmental patterning. It also includes embryos that develop at one end, but that slump at the other end into an amorphous mass, a phenotype most accurately described as roadkill. The failure of cellularization in most rdx6 germline clone embryos reflects severe defects during the early mitotic cycles. Abnormalities include mitotic asynchrony, uneven nuclear spacing, failed anaphase resolution and multipolar mitotic figures.
rdx6 homozygous clones are the same size as their wild-type counterparts in eye and wing imaginal discs.
In embryonic rdx6 germline clones mitoses are asynchronous, nuclear spacing is uneven, mitotic figures are highly abnormal, and much of the DNA sinks into the interior of the embryo.
rdx6 is a suppressor of metathoracic leg phenotype of Pc1
rdx6 is a suppressor of mesothoracic leg phenotype of Pc1
Based on embryonic and larval lethality, the following rdx alleles can be ranked from strongest to weakest as follows: rdx5 > rdx6 > rdx4 = rdx1.