TRPM7

transient receptor potential cation channel subfamily M member 7
OMIM: 605692, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber TRPM7 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • {Amyotrophic lateral sclerosis-parkinsonism/dementia complex, susceptibility to}, MIM# 105500
  • Cardiac arrhythmia, stillbirth

Amber TRPM7 in Fetal anomalies


Version 1.255

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Genomics England PanelApp
Phenotypes
  • Cardiac arrhythmia, stillbirth