{{Rsnum
|rsid=367543007
|Orientation=plus
|Chromosome=12
|geno1=(-;-)
|geno2=(-;CA)
|geno3=(CA;CA)
|Gene=ATP6V0A2
|position=123754417
|Gene_s=ATP6V0A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=12
|CLNACC=RCV000020685.2
|CLNALLE=1
|CLNDBN=Cutis laxa with osteodystrophy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK5200:C0268355:219200:90350:73856006
|CLNHGVS=NC_000012.11:g.124238964_124238965delCA
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK5200
|Disease=Cutis laxa with osteodystrophy
|FwdREF=CA
|REF=TCA
|RSPOS=124238963
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=367543007
|GENEINFO=ATP6V0A2:23545
|GENE_ID=23545
|GENE_NAME=ATP6V0A2
}}{{PMID Auto
|PMID=18157129
|Title=Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2.
}}

{{PMID Auto
|PMID=20301755
|Title=ATP6V0A2-Related Cutis Laxa
}}