Genopathy
Gene-Disorder Association · Article
Gene
CACNA1C
Calcium Voltage-Gated Channel Subunit Alpha1 C
Disorder
Brugada Syndrome 3
First reported 2007
Supporting publications 1
Key publication · gene–disorder Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death.Circulation · 2007
Key publication · disorder A single Na(+) channel mutation causing both long-QT and Brugada syndromes.Circulation research · 1999
Manually curated
Association Review

In brief

The association between CACNA1C (Calcium Voltage-Gated Channel Subunit Alpha1 C) and Brugada Syndrome 3 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.

Sources 4
Clinical variants 131
Symptoms 11
Compounds 0
Trials 0
Publications 1
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
CACNA1C

The gene

2 source summaries

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

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04
Brugada Syndrome 3

The disorder

9 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

6 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

131 clinical variants

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

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07
Mechanism overlap

Shared mechanisms

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

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08
Literature

Reading

1 publication

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

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09
Provenance

References & sources

8 references

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

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