hypomorphic allele - genetic evidence
Nucleotide substitution: G1008A. Amino acid replacement: E?K. Missense mutation within the homeodomain.
G15994564A
E268K | exd-PA; E268K | exd-PB; E268K | exd-PD; E268K | exd-PE
E?K
lethal | recessive
lethal - all die during embryonic stage | recessive
some die during embryonic stage | recessive