Tctn2 - tectonic family member 2

Predicted to enable proton transmembrane transporter activity. Predicted to be involved in cilium assembly; protein localization to ciliary transition zone; and smoothened signaling pathway. Predicted to be located in ciliary transition zone. Predicted to be part of MKS complex. Human ortholog(s) of this gene implicated in Joubert syndrome 24 and Meckel syndrome 8. Orthologous to human TCTN2 (tectonic family member 2). [provided by Alliance of Genome Resources, Apr 2022]