Genopathy
Gene-Disorder Association · Article
Gene
FLNC
Filamin C
Disorder
Cardiomyopathy, Familial Hypertrophic, 26
First reported 2014
Supporting publications 51
Key publication · gene–disorder Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy.Nature communications · 2014
Key publication · disorder [Clinical-pathological findings in a case of obstructive myocardiopathy].Zeitschrift fur Kardiologie · 1976
Manually curated
Association Review

In brief

The association between FLNC (Filamin C) and Cardiomyopathy, Familial Hypertrophic, 26 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and causative variation.

Sources 4
Clinical variants 4,716
Symptoms 33
Compounds 0
Trials 0
Publications 51
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

4 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
FLNC

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
Cardiomyopathy, Familial Hypertrophic, 26

The disorder

13 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Phenotype

Clinical features

13 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
ClinVar and variant evidence

Genetic basis

4,716 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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07
Population genetics

GWAS signals

1 GWAS phenotype

Gene-associated GWAS phenotypes matching the disorder, with best SNP, score, risk-allele frequency and effect size.

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08
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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09
Literature

Reading

51 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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10
Provenance

References & sources

15 references

Every source and publication cited across this dossier, as one numbered reference list.

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