The association between TCTN1 (Tectonic Family Member 1) and Joubert Syndrome 13 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.
Sources3
Clinical variants70
Symptoms7
Compounds0
Trials0
Publications4
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.