{{Rsnum
|rsid=137853263
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=OCRL
|position=129562396
|Gene_s=OCRL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300535
|variant=0006
|rsnum=137853263
}}{{ClinVar
|rsid=137853263
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=128696373
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=OCRL:4952
|GENE_NAME=OCRL
|GENE_ID=4952
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.128696373C>T
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=300535.0006; VAR_022698
|CLNSIG=5
|CLNCUI=C1845167
|CLNDBN=Dent disease 2; Lowe syndrome
|Disease=Dent disease 2; Lowe syndrome
|CLNACC=RCV000011608.6; RCV000059607.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK99494:C1845167:300555:1652:93623; NBK1480:C0028860:309000:534:79385002
}}{{PMID Auto
|PMID=17384968
|Title=OCRL1 mutations in patients with Dent disease phenotype in Japan.
}}

{{PMID Auto
|PMID=21031565
|Title=From Lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes.
}}
{{omim
|id=309000
|rsnum=137853263
}}