Genopathy
Gene-Disorder Association · Article
Gene
SCN5A
Sodium Voltage-Gated Channel Alpha Subunit 5
Disorder
Congenital Long Qt Syndrome
First reported 1996
Supporting publications 73
Key publication · gene–disorder Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome.Proceedings of the National Academy of Sciences of the United States of America · 1996
Key publication · disorder Inhibitors of polypeptide elongation on yeast polysomes.The Journal of antibiotics · 1975
Manually curated
Association Review

In brief

The association between SCN5A (Sodium Voltage-Gated Channel Alpha Subunit 5) and Congenital Long Qt Syndrome is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording pathogenic variants.

Sources 2
Clinical variants 237
Symptoms 0
Compounds 0
Trials 0
Publications 73
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

2 sources

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

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03
SCN5A

The gene

2 source summaries

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

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04
Congenital Long Qt Syndrome

The disorder

4 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

237 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

73 publications

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

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07
Provenance

References & sources

13 references

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

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