B3GALT6 (Beta-1,3-Galactosyltransferase 6) is a Protein Coding gene. Diseases associated with B3GALT6 include Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 1, With Or Without Fractures and Ehlers-Danlos Syndrome, Progeroid Type, 2. Among its related pathways are Glycosaminoglycan metabolism and Metabolism.