1. Genes and Genomic Entities
  2. KCNN4

KCNN4

potassium calcium-activated channel subfamily N member 4
OMIM: 602754, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green KCNN4 in Rare anaemia


Level 2: Haematology
Version 3.19
Latest signed off version: v3.0 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • North West GLH
  • Yorkshire and North East GLH
  • London South GLH
  • NHS GMS
  • Expert Review Green
  • Wessex and West Midlands GLH
Phenotypes
  • 616689 Dehydrated hereditary stomatocytosis 2
  • Hereditary Xerocytosis
Amber KCNN4 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.158
Latest signed off version: v6.0 (30 Apr 2025)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
Phenotypes
  • Dehydrated hereditary stomatocytosis 2, OMIM:616689