Genopathy
Gene-Disorder Association · Article
Gene
KCNA1
Potassium Voltage-Gated Channel Subfamily A Member 1
Disorder
Episodic Kinesigenic Dyskinesia 1
First reported 2021
Supporting publications 2
Key publication · gene–disorder Genetics of Paroxysmal Dyskinesia: Novel Variants Corroborate the Role of KCNA1 in Paroxysmal Dyskinesia and Highlight the Diverse Phenotypic Spectrum of KCNA1- and SLC2A1-Related Disorders.Frontiers in neurology · 2021
Key publication · disorder Physiological and therapeutic effects of bilateral intermediate midbrain crusotomy for atheto-dystonia; 10 cases.Transactions of the American Neurological Association · 1955
Manually curated
Association Review

In brief

The association between KCNA1 (Potassium Voltage-Gated Channel Subfamily A Member 1) and Episodic Kinesigenic Dyskinesia 1 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording likely-pathogenic variants and a causative germline mutation.

Sources 3
Clinical variants 1
Symptoms 19
Compounds 0
Trials 0
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

3 sources

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

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03
KCNA1

The gene

2 source summaries

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

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04
Episodic Kinesigenic Dyskinesia 1

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
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

1 clinical variant

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

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

11 references

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

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