KCNAB3

potassium voltage-gated channel subfamily A regulatory beta subunit 3
OMIM: 604111, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red KCNAB3 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Neurodevelopmental disorder (MONDO#0700092), KCNAB3-related

Red KCNAB3 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Neurodevelopmental disorder (MONDO#0700092), KCNAB3-related