{{Rsnum
|rsid=80359853
|Chromosome=8
|Orientation=plus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=ESCO2
|position=27777068
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ESCO2
}}{{omim
|id=609353
|rsnum=80359853
|variant=0004
}}{{ClinVar
|rsid=80359853
|Reversed=0
|FwdALT=A
|REF=G
|ALT=GA
|RSPOS=27634576
|CHROM=8
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=ESCO2:157570
|GENE_NAME=ESCO2
|GENE_ID=157570
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.27634585dupA
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1153; 609353.0004
|CLNSIG=5
|CLNCUI=C0392475
|CLNDBN=Roberts-SC phocomelia syndrome
|Disease=Roberts-SC phocomelia syndrome
|CLNACC=RCV000001808.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1153:C0392475:268300:269000:3103:48718006
}}{{PMID Auto
|PMID=16380922
|Title=Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation.
|OA=1
}}

{{PMID Auto
|PMID=18411254
|Title=The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.
}}