Genopathy
Gene-Disorder Association · Article
Gene
KCNJ8
Potassium Inwardly Rectifying Channel Subfamily J Member 8
Disorder
Congenital Long Qt Syndrome
First reported 1975
Key publication · disorder Inhibitors of polypeptide elongation on yeast polysomes.The Journal of antibiotics · 1975
Manually curated
Association Review

In brief

The association between KCNJ8 (Potassium Inwardly Rectifying Channel Subfamily J Member 8) and Congenital Long Qt Syndrome is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 0
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access
02
Provenance

Evidence and sources

1 source

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

Request access
03
KCNJ8

The gene

2 source summaries

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

Request access
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).

Request access
05
Provenance

References & sources

4 references

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

Request access