KCNJ11 gene mutation

Clinical significance

• KCNJ11 gene mutations are associated with
  • neonatal diabetes mellitus
  • familial hyperinsulinemic hypoglycemia type 2

More general terms

• gene mutation testing; gene mutation analysis

Additional terms

• inwardly-rectifying K+ channel J11; ATP-sensitive inward rectifier K+ channel 11; K+ channel, inwardly rectifying subfamily J member 11; inward rectifier K+ channel Kir6.2; IKATP (KCNJ11)