TRIP11 and odontochondrodysplasia 1: In humans, null mutations in TRIP11 are causative of achondrogenesis type 2A (ACG2A), while hypomorphic mutations have been identified in cases of odontochondrodysplasia (ODCD) (Upadhyai et al., 2021; Medina et al., 2020; Del Pino et al., 2021; Wehrle et al., 2019).