Point mutation (W362F) in the channel pore of Shal, a highly conserved residue whose mutation has been demonstrated to function as a pore-blocking mutation in mammalian cells and cultured Drosophila embryonic neurons.
TGG19573030TTT
W362F
Single codon mutation (W362F) in the channel pore of Shal generated with CRISPR-Cas9 gene editing, Requires two nucleotide substitutions in codon (TGG to TTT/C - specific nucleotide change not specified).