Genopathy
Gene-Disorder Association · Article
Gene
KCNJ2
Potassium Inwardly Rectifying Channel Subfamily J Member 2
Manually curatedApproved treatment annotated
Association Review

In brief

The association between KCNJ2 (Potassium Inwardly Rectifying Channel Subfamily J Member 2) and Atrial Fibrillation is reported, with clinical genetic testing available.

Sources 1
Clinical variants 1
Symptoms 3
Compounds 2
Trials 37of 231 via KCNJ2 compounds
Publications 2
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
KCNJ2

The gene

2 source summaries

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

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04
Atrial Fibrillation

The disorder

6 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

1 clinical variant

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

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06
Interventions

Therapeutics

2 compounds & drugs

Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.

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07
Human studies

Clinical trials

231 clinical trials

Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.

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08
Literature

Reading

2 publications

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

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09
Provenance

References & sources

9 references

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

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