Joubert Syndrome 16 (JBTS16)

Joubert Syndrome 16, also known as jbts16, is related to joubert syndrome 14 and meckel syndrome, type 2. An important gene associated with Joubert Syndrome 16 is TMEM138 (Transmembrane Protein 138), and among its related pathways/superpathways are Bardet-Biedl syndrome and Joubert syndrome. Affiliated tissues include kidney and brain, and related phenotypes are molar tooth sign on mri and oculomotor apraxia