PCARE Chromosome 2

Photoreceptor cilium actin regulator
190 variants 190 Health Risk

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What This Gene Does
The protein encoded by this gene is highly expressed in photoreceptors and may associate with the primary cilium of the outer segment. The encoded protein appears to undergo post-translational lipid modification. Nonsense and missense variants of this gene appear to cause a recessive form of retinitis pigmentosa. [provided by RefSeq, Jun 2010]
Associated Conditions (14)
Retinitis pigmentosa
Retinal dystrophy
Retinitis pigmentosa 54
PCARE-related disorder
Optic atrophy
Inborn genetic diseases
Cone-rod dystrophy
PCARE-related retinopathy
Cone-rod dystrophy 23
Autosomal recessive retinitis pigmentosa
Stargardt disease
See cases
Retinal disorder
Retinitis pigmentosa with macular involvement
Key Variants
All Variants (190)
RSID Category Clinical Significance Conditions
RS527236056 Health Risk Pathogenic Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa
RS555070980 Health Risk Pathogenic
RS745486206 Health Risk Pathogenic
RS750501256 Health Risk Pathogenic
RS750987123 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS753619551 Health Risk Pathogenic Retinal dystrophy, Autosomal recessive retinitis pigmentosa, Retinal dystrophy
RS755375197 Health Risk Pathogenic
RS757391015 Health Risk Pathogenic
RS761147595 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS763749755 Health Risk Pathogenic
RS766484593 Health Risk Pathogenic
RS766609529 Health Risk Pathogenic
RS767188967 Health Risk Pathogenic Retinitis pigmentosa 54, Retinitis pigmentosa 54
RS767286082 Health Risk Pathogenic
RS768682214 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS770881706 Health Risk Pathogenic
RS772325487 Health Risk Pathogenic Retinitis pigmentosa 54, Retinitis pigmentosa 54
RS774215025 Health Risk Pathogenic Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa
RS777103184 Health Risk Pathogenic Retinitis pigmentosa 54, Retinitis pigmentosa 54
RS777717614 Health Risk Pathogenic
RS778346520 Health Risk Pathogenic
RS779886453 Health Risk Pathogenic Retinitis pigmentosa 54, Stargardt disease, Retinitis pigmentosa 54
RS794728002 Health Risk Pathogenic Retinitis pigmentosa 54, Retinitis pigmentosa, Autosomal recessive retinitis pigmentosa
RS863223344 Health Risk Pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS866543181 Health Risk Pathogenic Retinal dystrophy, Autosomal recessive retinitis pigmentosa, Retinal dystrophy
RS886044002 Health Risk Pathogenic
RS886044003 Health Risk Pathogenic
RS886044135 Health Risk Pathogenic
RS902856341 Health Risk Pathogenic
RS1553354660 Health Risk Pathogenic/Likely pathogenic
RS1558488513 Health Risk Pathogenic/Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS1558490060 Health Risk Pathogenic/Likely pathogenic Retinal dystrophy, Retinitis pigmentosa 54, Retinitis pigmentosa
RS1572827477 Health Risk Pathogenic/Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa 54, Retinitis pigmentosa
RS1667476173 Health Risk Pathogenic/Likely pathogenic Retinitis pigmentosa 54, Autosomal recessive retinitis pigmentosa, PCARE-related disorder
RS1667480949 Health Risk Pathogenic/Likely pathogenic Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa
RS1667506537 Health Risk Pathogenic/Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS367658438 Health Risk Pathogenic/Likely pathogenic Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa 54
RS369937337 Health Risk Pathogenic/Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa 54, Retinitis pigmentosa
RS748396645 Health Risk Pathogenic/Likely pathogenic Retinal dystrophy, Retinitis pigmentosa 54, Retinitis pigmentosa with macular involvement
RS762973163 Health Risk Pathogenic/Likely pathogenic Retinal dystrophy, Retinal dystrophy
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