The association between KCNJ6 (Potassium Inwardly Rectifying Channel Subfamily J Member 6) and Keppen-Lubinsky Syndrome is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and a causative germline mutation.
Sources5
Clinical variants11
Symptoms68
Compounds0
Trials0
Publications3
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.