{{Rsnum
|rsid=281875361
|Chromosome=1
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=ZMPSTE24
|position=40258325
|Gene_s=ZMPSTE24
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=GT
|CHROM=1
|CLNACC=RCV000023548.2
|CLNALLE=1
|CLNDBN=Lethal tight skin contracture syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0406585:275210:ORPHA1662:400128006
|CLNHGVS=NC_000001.11:g.40258325dupT
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_005857.4:c.54_55insT; 606480.0007
|Disease=Lethal tight skin contracture syndrome
|FwdALT=T
|REF=G
|RSPOS=40258324
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;NSF;REF;ASP;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168001205000002110200
|WGT=1
|dbSNPBuildID=137
|rsid=281875361
|GENEINFO=ZMPSTE24:10269
|GENE_ID=10269
|GENE_NAME=ZMPSTE24
}}{{PMID Auto
|PMID=16297189
|Title=Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy.
|OA=1
}}

{{PMID Auto
|PMID=20635340
|Title=Restrictive dermopathy and ZMPSTE24 mutations in Mennonites: Evidence for allelic heterogeneity.
}}