Mutations in the TRIP11 gene encoding GMAP210 are causative of the human skeletal diseases achondrogenesis type 1A and odontochondrodysplasia (Costantini et al., 2021; Del Pino et al., 2021; Medina et al., 2020; Qian et al., 2021; Smits et al., 2010; Upadhyai et al., 2021; Wehrle et al., 2019; Yeter et al., 2022). Here, TRIP11 is linked to odontochondrodysplasia.