OCRL Chromosome X

OCRL inositol polyphosphate-5-phosphatase
159 variants 159 Health Risk

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What This Gene Does
This gene encodes an inositol polyphosphate 5-phosphatase. This protein is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans-Golgi network, clathrin-coated vesicles and, endosomes and the plasma membrane. This protein may also play a role in primary cilium formation. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Gene Info
Gene Group
Phosphoinositide phosphatases
Locus Type
gene with protein product
Location
Xq26.1
Ensembl
ENSG00000122126
Associated Conditions (13)
Lowe syndrome
Dent disease type 2
Nephrolithiasis/nephrocalcinosis
Thyroid cancer
nonmedullary
1
Nonpapillary renal cell carcinoma
OCRL-related disorder
Developmental cataract
Genetic developmental and epileptic encephalopathy
Epilepsy
Dent disease
Neurodevelopmental delay
Key Variants
All Variants (159)
RSID Category Clinical Significance Conditions
RS1602783564 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS1602802640 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS1602820970 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS1936131926 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS1936229983 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS1936266464 Health Risk Likely pathogenic
RS2124404743 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2124412853 Health Risk Likely pathogenic
RS2124417903 Health Risk Likely pathogenic
RS2124417909 Health Risk Likely pathogenic Dent disease type 2, Nonpapillary renal cell carcinoma, Nephrolithiasis/nephrocalcinosis
RS2124418469 Health Risk Likely pathogenic
RS2124428298 Health Risk Likely pathogenic Lowe syndrome, Nonpapillary renal cell carcinoma, Lowe syndrome
RS2521838917 Health Risk Likely pathogenic Dent disease type 2, Dent disease type 2
RS2521838949 Health Risk Likely pathogenic Dent disease type 2, Dent disease type 2
RS2521855742 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521873170 Health Risk Likely pathogenic Dent disease type 2, Dent disease type 2
RS2521873405 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521877934 Health Risk Likely pathogenic
RS2521878560 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521889054 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521889385 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521889771 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521906115 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521906131 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521906486 Health Risk Likely pathogenic Dent disease, Dent disease
RS2521918360 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521920142 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521920349 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521920631 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521922221 Health Risk Likely pathogenic Lowe syndrome, Lowe syndrome
RS2521943150 Health Risk Likely pathogenic Dent disease type 2, Dent disease type 2
RS398123289 Health Risk Likely pathogenic Thyroid cancer, nonmedullary, 1
RS794727137 Health Risk Likely pathogenic
RS1057515577 Health Risk Pathogenic Lowe syndrome, Lowe syndrome
RS1057520078 Health Risk Pathogenic
RS1057520613 Health Risk Pathogenic
RS1182741031 Health Risk Pathogenic Lowe syndrome, Nephrolithiasis/nephrocalcinosis, Lowe syndrome
RS137853260 Health Risk Pathogenic Lowe syndrome, Lowe syndrome
RS137853261 Health Risk Pathogenic Lowe syndrome, Lowe syndrome
RS137853262 Health Risk Pathogenic Dent disease type 2, Dent disease type 2
RS137853846 Health Risk Pathogenic Dent disease type 2, Lowe syndrome, Dent disease type 2
RS137853858 Health Risk Pathogenic Lowe syndrome, Lowe syndrome
RS1427698686 Health Risk Pathogenic Lowe syndrome, Lowe syndrome
RS1556345889 Health Risk Pathogenic Lowe syndrome, Lowe syndrome
RS1556346271 Health Risk Pathogenic
RS1556346316 Health Risk Pathogenic Lowe syndrome, Lowe syndrome
RS1569463775 Health Risk Pathogenic Lowe syndrome, Dent disease type 2, Lowe syndrome
RS1602780580 Health Risk Pathogenic
RS1602782195 Health Risk Pathogenic Lowe syndrome, Lowe syndrome
RS1602791255 Health Risk Pathogenic Lowe syndrome, Lowe syndrome
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