Lacks most of the homeodomain.
Deletion of amino acids 274 to 302 (including the homeodomain).
embryonic epidermis
parasegment
parasegment 1
parasegment 3
parasegment 5
parasegment 7
parasegment 9
parasegment 11
parasegment 13
parasegment 15
en stripes.
Can induce the anti-ftz phenotype: mutant embryos are deficient for cuticular structures derived from the odd numbered parasegments. Also transforms ftz11 or ftz13 embryos towards the anti-ftz phenotype.
Strong ftz phenotype.