TRIP11 and achondrogenesis type IA: Mutations in the thyroid hormone receptor interactor 11 (TRIP11) gene encoding the Golgi-associated microtubule-binding protein 210 (GMAP210) in the human population give rise to a lethal neonatal skeletal dysplasia termed as achondrogenesis (ACG1A) type IA or the much milder nonlethal odontochondrodysplasia (ODCD) depending on whether the mutation leads to a complete or partial loss of function [63,64,65,66,67].