Amino acid replacement: W465term.
G7816341A
W465term | LanB1-PA; W465term | LanB1-PB
W465term
G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation (exact site of mutation unspecified). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Mutant embryos show alary muscle and dorsal vessel defects, and severe midgut constriction defects and visceral mesoderm phenotypes. They also show pronounced defects in the heart and in somatic body wall muscles.
Col4a1S3064, LanB1S0473 has partially lethal - majority die phenotype