ESCO1

establishment of sister chromatid cohesion N-acetyltransferase 1

Summary

Enables identical protein binding activity; protein-lysine-acetyltransferase activity; and zinc ion binding activity. Involved in peptidyl-lysine acetylation; post-translational protein acetylation; and regulation of DNA replication. Located in chromatin. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants36 total

rsidPosition (GRCh37)AllelesClassClinVar
rs13961253818:19,111,215C/Tintron variant—
rs117635218018:19,112,586G/C—uncertain significance
rs134904699518:19,116,005A/T—uncertain significance
rs128560038218:19,144,182A/C—uncertain significance
rs14676504518:19,144,237T/C—uncertain significance
rs130521760018:19,144,253G/C—uncertain significance
rs14038890918:19,146,128G/T—uncertain significance
rs122626333418:19,147,974C/A—uncertain significance
rs77768898618:19,148,042C/G—uncertain significance
rs75810883118:19,153,280T/G—uncertain significance
rs14891752718:19,153,285G/A—uncertain significance
rs14371645018:19,153,304T/C—uncertain significance
rs203836971818:19,153,481T/C—uncertain significance
rs14752875518:19,153,647C/G—uncertain significance
rs75936741918:19,153,715G/A—uncertain significance
rs74828969718:19,153,792T/C—uncertain significance
rs54348137218:19,153,822A/G—uncertain significance
rs14863248518:19,153,832A/G—uncertain significance
rs203837849018:19,153,921G/A—uncertain significance
rs37261659218:19,153,946G/C—uncertain significance
rs37659896518:19,153,976G/C—uncertain significance
rs77876108618:19,154,034C/T—likely benign
rs36969712718:19,154,095G/A—uncertain significance
rs76239194418:19,154,164C/A—uncertain significance
rs37366597118:19,154,168C/A—uncertain significance
rs126543838918:19,154,173T/C—uncertain significance
rs101991374318:19,154,305G/C—uncertain significance
rs14624953618:19,154,339T/C—uncertain significance
rs203839170318:19,154,443C/T—uncertain significance
rs144316307118:19,154,456G/C—uncertain significance
rs20116590318:19,154,522G/C—uncertain significance
rs76629586518:19,154,570C/T—likely benign
rs126506803818:19,154,597A/G—uncertain significance
rs132286121618:19,154,600T/C—uncertain significance
rs140871550918:19,154,641C/T—uncertain significance
rs76735540318:19,154,779T/G—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.