TECT2 Rabbit Polyclonal Antibody, 20ul Protein Modification Mutations in this gene are

Mutations in this gene are also associated with hyperphosphatemic familial tumoral calcinosis (HFTC)

Three pseudogenes have been mapped

which recognizes the 7-methylguanosine cap structure at the 5' end of messenger RNAs

Orphan receptor with constitutive G(i) signaling activity that activate cyclic AMP

TECT2 Rabbit Polyclonal Antibody, 20ul Protein Modification Mutations in this gene areThis gene encodes a type I membrane protein that belongs to the tectonic family. Studies in mice suggest that this protein may be involved in hedgehog signaling and essential for ciliogenesis. Mutations in this gene are associated with Meckel syndrome type 8. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.