NEXN

nexilin F-actin binding protein
OMIM: 613121, Gene2Phenotype

10 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 10 panels
Green NEXN in Dilated Cardiomyopathy Level 2: Cardiovascular disorders Version 1.48 Component of the following Super Panels: Adult Cardiac SuperPanel Cardiomyopathy_Adult_SuperPanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, dilated, 1CC, MIM# 613122 Tags for review
Red NEXN in Hypertrophic cardiomyopathy_HCM Level 2: Cardiovascular disorders Version 1.10 Component of the following Super Panels: Adult Cardiac SuperPanel Cardiomyopathy_Adult_SuperPanel	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, hypertrophic, 20, MIM# 613876
Green NEXN in Hydrops fetalis Level 2: Dysmorphic and congenital abnormality syndromes Version 0.328	2 reviews	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Cardiomyopathy, dilated, 2M, autosomal recessive, MIM# 621261
Green NEXN in Mendeliome Version 1.3512	2 reviews	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, dilated, 2M, autosomal recessive, MIM# 621261 Cardiomyopathy, dilated 1CC - MIM#613122
Red NEXN in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.565	1 review	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Lethal fetal cardiomyopathy Hydrops fetalis Cardiomyopathy, dilated 1CC - MIM#613122
Green NEXN in Cardiomyopathy_Paediatric Level 2: Cardiovascular disorders Version 0.207	2 reviews	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green London South GLH South West GLH NHS GMS Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, dilated, 2M, autosomal recessive, MIM# 621261 Cardiomyopathy, familial hypertrophic, 20, Cardiomyopathy, dilated, 1CC
Red NEXN in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category C gene Phenotypes Cardiomyopathy, familial hypertrophic Cardiomyopathy, dilated
Green NEXN in Fetal anomalies Version 1.465	1 review	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Lethal fetal cardiomyopathy Hydrops fetalis Cardiomyopathy, dilated 1CC - MIM#613122
Red NEXN in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category C gene Expert Review Red Phenotypes Cardiomyopathy, familial hypertrophic Cardiomyopathy, dilated
Green NEXN in Transplant Co-Morbidity Level 2: Screening Version 0.20	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, dilated, 1CC, MIM# 613122