Genomics England
GMS Panels
Panels
Genes and Entities

TNNC2

troponin C2, fast skeletal type
OMIM: 191039
PanelMode of inheritanceDetails
1 panel
Green
in Congenital muscular dystrophy and congenital myopathy
Component of the following Super Panels:
  • - Hypotonic infant
  • - Other rare neuromuscular disorders
R-numbers: R432
Signed-off version 1.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Myopathy, congenital, with neonatal respiratory insufficiency, OMIM:620161