Meckelin Products


Description

Meckelin localizes to the primary cilium and to the plasma membrane. It functions in centriole migration to the apical membrane and formation of the primary cilium. Defects in the gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6).

Bioinformatics

Entrez Rat
Mouse
Human
Uniprot Human
Product By Gene ID 91147
Alternate Names
  • meckel syndrome type 3 protein
  • MECKELIN
  • Meckelin
  • MGC26979
  • TNEM67
  • transmembrane protein 67