TNNI3

troponin I3, cardiac type
OMIM: 191044, Gene2Phenotype

9 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 9 panels
Green TNNI3 in Dilated Cardiomyopathy Level 2: Cardiovascular disorders Version 1.48 Component of the following Super Panels: Adult Cardiac SuperPanel Cardiomyopathy_Adult_SuperPanel	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, dilated, 1FF, MIM#613286 Tags for review
Green TNNI3 in Hypertrophic cardiomyopathy_HCM Level 2: Cardiovascular disorders Version 1.10 Component of the following Super Panels: Adult Cardiac SuperPanel Cardiomyopathy_Adult_SuperPanel	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, hypertrophic, 7, MIM# 613690
Green TNNI3 in Incidentalome Version 0.360	3 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services 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 1.130	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance 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 0.207	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green London South GLH South West GLH NHS GMS Phenotypes Cardiomyopathy, dilated, 2A, Cardiomyopathy, familial hypertrophic, 7 Cardiomyopathy, dilated, 1FF Hypertrophic cardiomyopathy
Amber TNNI3 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber BabySeq Category B gene Phenotypes Familial hypertrophic cardiomyopathy Cardiomyopathy, dilated
Red TNNI3 in Incidentalome_PREGEN_DRAFT Version 0.43	1 review	Unknown	Sources Expert Review Red NSW Health Pathology
Amber TNNI3 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category B gene Expert Review Amber Phenotypes Familial hypertrophic cardiomyopathy Cardiomyopathy, dilated
Green TNNI3 in Transplant Co-Morbidity Level 2: Screening Version 0.20	0 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, dilated, 1FF, MIM# 613286 Cardiomyopathy, hypertrophic, 7 , MIM#613690 Cardiomyopathy, familial restrictive, MIM#1 115210