Amino acid replacement: ?148term.
G1705839A
W148term | cpb-PA; W148term | cpb-PB
?148term
G to A nucleotide change at the second or third position of the wild type Trp codon leads to a nonsense mutation (exact site of mutation unspecified). The mutation was annotated at the second base of the codon.
cpb[+]/cpbF44, mir-8Δ has abnormal neuroanatomy | dominant | third instar larval stage phenotype
cpb[+]/cpbF44, mir-8Δ has NMJ bouton | third instar larval stage phenotype
cpb[+]/cpbF44, mir-8Δ has embryonic/larval neuromuscular junction | third instar larval stage phenotype
Isolated in an EMS screen for failure to complement cpbM143 lethality.