TNNI3:Ensemblv115

troponin I3, cardiac type
OMIM: 191044, ClinGen, DECIPHER

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green TNNI3 in Dilated Cardiomyopathy


Level 2: Cardiovascular disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Cardiomyopathy, dilated, 1FF, MIM#613286
Tags
  • for review

Green TNNI3 in Hypertrophic cardiomyopathy_HCM


Level 2: Cardiovascular disorders
Version 2.0

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Cardiomyopathy, hypertrophic, 7, MIM# 613690

Green TNNI3 in Incidentalome


Version 1.0

3 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Victorian Clinical Genetics Services
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Cardiomyopathy, dilated, 1FF, MIM#613286
  • Cardiomyopathy, hypertrophic, 7, MIM# 613690
  • Cardiomyopathy, familial restrictive, MIM#1115210
Tags
  • cardiac

Green TNNI3 in Additional findings_Adult


Level 2: Screening
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Melbourne Genomics Health Alliance
  • Expert Review Green
Phenotypes
  • Cardiomyopathy, dilated, 1FF, MIM# 613286
  • Cardiomyopathy, familial restrictive, MIM#1 115210
  • Cardiomyopathy, hypertrophic, 7 , MIM#613690

Green TNNI3 in Cardiomyopathy_Paediatric


Level 2: Cardiovascular disorders
Version 1.0

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • South West GLH
  • London South GLH
  • Expert Review Green
Phenotypes
  • Cardiomyopathy, dilated, 2A,
  • Cardiomyopathy, familial hypertrophic, 7
  • Cardiomyopathy, dilated, 1FF
  • Hypertrophic cardiomyopathy

Amber TNNI3 in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 2.0

0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • BabySeq Category B gene
Phenotypes
  • Familial hypertrophic cardiomyopathy
  • Cardiomyopathy, dilated

Green TNNI3 in Transplant Co-Morbidity


Level 2: Screening
Version 1.0

0 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Cardiomyopathy, dilated, 1FF, MIM# 613286
  • Cardiomyopathy, hypertrophic, 7 , MIM#613690
  • Cardiomyopathy, familial restrictive, MIM#1 115210