Name

TMEM67 Gene

transmembrane protein 67

The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). [provided by RefSeq, Nov 2008]

TMEM67 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for TMEM67 from the Pathway Commons Protein-Protein Interactions dataset.