ESCO1 (Establishment Of Sister Chromatid Cohesion N-Acetyltransferase 1) is a Protein Coding gene. Diseases associated with ESCO1 include Roberts Syndrome and Anonychia Congenita. Among its related pathways are CDK-mediated phosphorylation and removal of Cdc6 and Cell Cycle, Mitotic. ESCO1 belongs to a conserved family of acetyltransferases involved in sister chromatid cohesion.