hypomorphic allele - genetic evidence
Nucleotide substitution: C2393T. Amino acid replacement: L127F. Within the homeobox.
2393 C --> T; 127 leu --> phe
C6758294T
C2393T
L122F | bcd-PD; L51F | bcd-PE; L46F | bcd-PF; L127F | bcd-PG
L127F
lethal - all die during embryonic stage | maternal effect
some die during embryonic stage | maternal effect
Intermediate bcd allele.
Weak bcd allele.
hb protein expression in early bcd9 mutant embryos has been studied.
Intermediate bcd allele.
Weak bcd allele.
hb protein expression in early bcd9 mutant embryos has been studied.