Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2318
Gene Symbol: FLNC
FLNC 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy. 26666891 2016
Entrez Id: 2318
Gene Symbol: FLNC
FLNC 		0.700 GeneticVariation disease CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349 2016
Entrez Id: 2318
Gene Symbol: FLNC
FLNC 		0.700 CausalMutation disease CLINVAR FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy. 28008423 2016
Entrez Id: 2318
Gene Symbol: FLNC
FLNC 		0.700 CausalMutation disease CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349 2016
Entrez Id: 2318
Gene Symbol: FLNC
FLNC 		0.700 CausalMutation disease CLINVAR Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy: Outcomes and Lessons Learned. 26436962 2015
Entrez Id: 2318
Gene Symbol: FLNC
FLNC 		0.700 CausalMutation disease CLINVAR Prioritizing causal disease genes using unbiased genomic features. 25633252 2014
Entrez Id: 2318
Gene Symbol: FLNC
FLNC 		0.700 CausalMutation disease CLINVAR LOVD v.2.0: the next generation in gene variant databases. 21520333 2011
Entrez Id: 2318
Gene Symbol: FLNC
FLNC 		0.700 GeneticVariation disease UNIPROT Mutations in the N-terminal actin-binding domain of filamin C cause a distal myopathy. 21620354 2011
Entrez Id: 2318
Gene Symbol: FLNC
FLNC 		0.700 GermlineCausalMutation disease ORPHANET Mutations in the N-terminal actin-binding domain of filamin C cause a distal myopathy. 21620354 2011
Entrez Id: 2318
Gene Symbol: FLNC
FLNC 		0.700 Biomarker disease GENOMICS_ENGLAND A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy. 15929027 2005
Entrez Id: 2318
Gene Symbol: FLNC
FLNC 		0.700 Biomarker disease CTD_human