amorphic allele - genetic evidence
Indel within hkb that results in a frameshift after only 5 residues.
A 19bp deletion and 9bp insertion (TCCCTGGGA) starting in codon N5 of hkb leads to a frameshift and early translation termination.
TCCCTGGGA
abnormal cell migration | embryonic stage
decreased size | embryonic stage
lethal - all die during embryonic stage
embryonic/larval gut | embryonic stage
embryonic/larval salivary gland | embryonic stage