TRPM4

transient receptor potential cation channel subfamily M member 4
OMIM: 606936, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber TRPM4 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Progressive familial heart block, type IB, MIM# 604559
  • Erythrokeratodermia variabilis et progressiva 6, MIM# 618531

Red TRPM4 in Palmoplantar Keratoderma and Erythrokeratoderma


Level 2: Dermatological disorders
Version 0.132

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert Review
Phenotypes
  • Erythrokeratodermia variabilis et progressiva 6, MIM# 618531

Green TRPM4 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • BabySeq Category A gene
  • Expert Review Green
Phenotypes
  • Cardiac conduction disease

Amber TRPM4 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.113

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • BabySeq Category A gene
Phenotypes
  • Progressive familial heart block, type IB 604559
Tags
  • for review
  • cardiac