SMCHD1
Structural Maintenance of Chromosomes flexible Hinge Domain Containing 1 is a protein that in humans is encoded by the SMCHD1 gene. Mutations in SMCHD1 are causative for development of facioscapulohumeral muscular dystrophy type 2 and Bosma arhinia microphthalmia syndrome.
Without maternal SMCHD1 in the egg cell, children bear with altered skeletal structures.