CBX1 and Hutchinson-Gilford progeria syndrome: CBX1 (Chromobox 1) is a Protein Coding gene. Diseases associated with CBX1 include Hyperoxaluria, Primary, Type I and Hutchinson-Gilford Progeria Syndrome. Among its related pathways are HCMV Infection and Chromatin Regulation/Acetylation. Gene Ontology (GO) annotations related to this gene include protein homodimerization activity and chromatin binding. An important paralog of this gene is CBX3