KCNJ18

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

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red KCNJ18 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert Review
Phenotypes
  • {Thyrotoxic periodic paralysis, susceptibility to, 2}, MIM# 613239

Red KCNJ18 in Skeletal Muscle Channelopathies


Level 2: Neurology and neurodevelopmental disorders
Version 1.1

Component of the following Super Panels:

  • Myopathy Superpanel
  • Neuromuscular Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert list
    • Expert Review
    Phenotypes
    • Hypokalemic periodic paralysis
    • {Thyrotoxic periodic paralysis, susceptibility to, 2}, MIM# 613239

    Red KCNJ18 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    Phenotypes
    • Hypokalaemic periodic paralysis

    Red KCNJ18 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • BabySeq Category C gene
    • Expert Review Red
    Phenotypes
    • Hypokalaemic periodic paralysis