This Panel is marked as Retired
Dilated Cardiomyopathy (DCM)
Gene: FLNC
FLNC (filamin C)
EnsemblGeneIds (GRCh38): ENSG00000128591
EnsemblGeneIds (GRCh37): ENSG00000128591
OMIM: 102565, Gene2Phenotype
FLNC is in 11 panels
EnsemblGeneIds (GRCh38): ENSG00000128591
EnsemblGeneIds (GRCh37): ENSG00000128591
OMIM: 102565, Gene2Phenotype
FLNC is in 11 panels
1 review
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)
Variants in this GENE are reported as part of current diagnostic practice
Details
- Sources
-
- OMIM
- 102565
- Clinvar variants
- Variants in FLNC
- Penetrance
- Complete
- Panels with this gene
-
- Progressive cardiac conduction disease
- Arthrogryposis
- Paediatric or syndromic cardiomyopathy
- Hypertrophic cardiomyopathy
- Congenital myopathy
- Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies
- Dilated and arrhythmogenic cardiomyopathy
- Dilated Cardiomyopathy and conduction defects
- Arrhythmogenic right ventricular cardiomyopathy
- Fetal anomalies
- Distal myopathies
History Filter Activity
11 Feb 2016, Gel status: 0
Approved Gene
Caroline Wright (Genomics England Curator)This proposed gene was validated and added to this panel
6 Jan 2016, Gel status: 0
Created
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)FLNC was created by OxfordGenetics
6 Jan 2016, Gel status: 0
Added New Source
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)FLNC was added to Dilated Cardiomyopathy (DCM)panel. Sources: Oxford Medical Genetics Laboratory