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The protein encoded by TMEM67 localizes to the primary cilium and to the plasma membrane. Additionally we are shipping and many more products for this protein.
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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).
transmembrane protein 67
, meckel syndrome type 3 protein
, meckel syndrome type 3 protein homolog
, Meckel syndrome type 3 protein homolog
, Wistar polycystic kidney