Nucleotide substitution: ?514. A single nucleotide deletion (corresponding to amino acid residue 173) is predicted to cause a frameshift alteration in the sequence of the protein, followed by a premature stop codon at nucleotide 689 (amino acid residue 232). This truncates the protein within the kinase domain and also deletes other conserved sequence motifs near the C-terminus of the protein.
Position of mutation on reference sequence inferred by FlyBase curator based on author statement. Mutation is a 1 bp deletion in codon 173 which leads to a frameshift and a 232 aa long protein. GAC CGA becomes ACC GAC. Identical mutation to Myt11.
