Genopathy
Gene-Disorder Association · Article
Gene
CLCN2
Chloride Voltage-Gated Channel 2
Disorder
Epilepsy
First reported 2009
Supporting publications 1
Key publication · gene–disorder Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy.Human mutation · 2009
Key publication · disorder [Differential diagnosis of genuine and so-called traumatic epilepsy].Archiv fur Psychiatrie und Nervenkrankheiten, vereinigt mit Zeitschrift fur die gesamte Neurologie und Psychiatrie · 1950
Manually curated
Association Review

In brief

The association between CLCN2 (Chloride Voltage-Gated Channel 2) and Epilepsy is reported, with clinical genetic testing available.

Sources 1
Clinical variants 2
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

1 source

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

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03
CLCN2

The gene

1 source summary

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

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04
Epilepsy

The disorder

11 database identifiers

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

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05
ClinVar and variant evidence

Genetic basis

2 clinical variants

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

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06
Literature

Reading

1 publication

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

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07
Provenance

References & sources

5 references

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

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