Stop codon before the first finger domain.
Stage 13 ventral cords exhibit lack of longitudinal connectives, missing or disorganised commissures. Increase in the number of neuroblast sublineages expressing nub in all CNS ganglia.
Cuticle phenotype.
fkh1, hb4, kni10, tll1 has abnormal cell polarity | gastrula stage phenotype
hb4, nanosL7 has embryonic abdominal segment phenotype, suppressible by mxcG48
hb4, nanosL7 has embryonic abdominal segment phenotype, suppressible by Df(2R)vg-B
hb4, nanosL7 has embryonic abdominal segment phenotype, suppressible | partially by phob
hb4, nanosL7 has abdominal tergite phenotype, suppressible by mxcG48
hb4 is a suppressor of embryonic abdominal segment phenotype of nanosL7
hb4, nanosL7 has embryonic abdominal segment phenotype
hb4, nanosL7 has abdominal 7 ventral denticle belt phenotype
hb4, nanosL7 has abdominal 4 ventral denticle belt phenotype
hb4, mxcG48, nanosL7 has abdominal tergite phenotype
hb4, nanosL7 has abdominal 5 ventral denticle belt phenotype
hb4, nanosL7 has abdominal 8 ventral denticle belt phenotype
hb4, nanosL7 has abdominal tergite phenotype
hb4, nanosL7 has abdominal 1 ventral denticle belt phenotype
hb4, nanosL7 has abdominal 2 ventral denticle belt phenotype
hb4, nanosL7 has abdominal 3 ventral denticle belt phenotype
hb4, nanosL7 has abdominal 6 ventral denticle belt phenotype
Embryos derived from hb4 nosL7/nosL7 females differentiate only a few abdominal denticle belts. No rescue of abdominal segments is seen if the females also carry Df(1)10-70d, Df(1)mxc-1, mxc22a-6 or mxc1. Rescue of abdominal segments in embryos derived from hb4 nosL7/nosL7 females is seen if the females are also carrying mxcG48. Adult escapers have abnormal tergites and are mostly fertile. Rescue of abdominal segments in embryos derived from hb4 nosL7/nosL7 females is seen if the females are also carrying Df(2R)vg-B or phob.
hb4 is partially rescued by hbhb.0.7bcd
hb4 is partially rescued by hbDvir\hb.0.8bcd
Head segments and thoracic segments (except for T2) can be rescued by hbhb.0.7bcd or hbDvir\hb.0.8bcd.
Class I allele.
hbDrv2 fails to complement hb4.
Phenotypic class I.