Amino acid replacement: Q127term.
Nucleotide substitution: C?T.
C23026073T
C?T
Q127term | lmd-PB
Q127term
Mutant embryos show widespread pericardial cell hyperplasia.
The extent of myoblast fusion in lmd1 mutant embryos is significantly reduced compared to wild type.
Defects in the somatic muscle lineage are seen in homozygous and lmd1/Df(3R)M95A embryos, starting at late stage 12. Multinucleate Mhc-positive muscle fibres are not seen, instead only elongated, mononucleate Mhc-positive muscle cells are seen at late stage 15. Gut constrictions appear to be normal. Founder cells are present in mutant embryos but do not appear to undergo cell fusion (as occurs in wild-type embryos).
lmd1, trkunspecified has embryonic/larval tracheal system | embryonic stage phenotype