The human disease-relevant K242N mutation is knocked into endogenous Irk2.
G23514957Y
K242N | Irk2-PA; K226N | Irk2-PB; K226N | Irk2-PC; K242N | Irk2-PD
K242N
Analogous mutation in human KCNJ10 implicated in episodic kinesigenic dyskinesia, SGIP1-related; mutation carried on in vitro construct; site of nucleotide substitution in fly gene inferred by FlyBase curator based on reported amino acid change.