KCNJ18

potassium voltage-gated channel subfamily J member 18
OMIM: 613236, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red KCNJ18 in Skeletal Muscle Channelopathies

Level 3: Channelopathies
Level 2: Neurology and neurodevelopmental disorders
Version 1.46

review Not set
Sources
  • Expert Review Red
  • UKGTN
Phenotypes
  • Hypokalemic Periodic Paralysis, Type 1
Tags
  • ensembl_ids_known_missing
Red KCNJ18 in Paroxysmal central nervous system disorders


Version 3.10
Latest signed off version: v3.0 (22 Mar 2023)

review Not set
Sources
  • Expert Review Red
  • NHS GMS
  • London North GLH
  • Wessex and West Midlands GLH
Phenotypes
  • Thyrotoxic periodic paralysis, susceptibility to, 2, 613239
  • Hypokalemic Periodic Paralysis, Type 1
Tags
  • ensembl_ids_known_missing