PRPH2 Chromosome 6

Peripherin 2
309 variants 309 Health Risk

Upload your DNA to see your personal genotypes for variants in PRPH2.

What This Gene Does
The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein found in the outer segment of both rod and cone photoreceptor cells. It may function as an adhesion molecule involved in stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. This protein is essential for disk morphogenesis. Defects in this gene are associated with both central and peripheral retinal degenerations. Some of the various phenotypically different disorders are autosomal dominant retinitis pigmentosa, progressive macular degeneration, macular dystrophy and retinitis pigmentosa digenic. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Tetraspanins
Locus Type
gene with protein product
Location
6p21.1
Ensembl
ENSG00000112619
Associated Conditions (35)
Patterned macular dystrophy 1
Retinitis pigmentosa
Adult-onset foveomacular vitelliform dystrophy
Pigmentary retinal dystrophy
Cone-rod dystrophy
Choroidal dystrophy
central areolar 2
Macular dystrophy
PRPH2-related disorder
Retinal dystrophy
Stargardt disease
Vitelliform macular dystrophy 2
Retinitis pigmentosa 7
Retinal disorder
Usher syndrome
Patterned dystrophy of the retinal pigment epithelium
Vitelliform macular dystrophy 3
Optic atrophy
Blurred vision
Abnormal retinal pigmentation
+15 more conditions
Key Variants
RS113384495
Conflicting classifications of pathogenicity
Patterned macular dystrophy 1, Retinitis pigmentosa, Adult-onset foveomacular vitelliform dystrophy
Health Risk
RS139177846
Conflicting classifications of pathogenicity
Cone-rod dystrophy, Patterned macular dystrophy 1, Retinitis pigmentosa
Health Risk
RS139185976
Conflicting classifications of pathogenicity
Macular dystrophy, Patterned macular dystrophy 1, PRPH2-related disorder
Health Risk
RS139329966
Conflicting classifications of pathogenicity
Pigmentary retinal dystrophy, Retinitis pigmentosa, Choroidal dystrophy
Health Risk
RS139936445
Conflicting classifications of pathogenicity
Patterned macular dystrophy 1, Adult-onset foveomacular vitelliform dystrophy, Cone-rod dystrophy
Health Risk
RS140227298
Conflicting classifications of pathogenicity
Patterned macular dystrophy 1, Cone-rod dystrophy, Choroidal dystrophy
Health Risk
RS1442844778
Conflicting classifications of pathogenicity
Retinal dystrophy, Retinal dystrophy, PRPH2-related disorder
Health Risk
RS146703538
Conflicting classifications of pathogenicity
PRPH2-related disorder, Adult-onset foveomacular vitelliform dystrophy, Cone-rod dystrophy
Health Risk
RS150381599
Conflicting classifications of pathogenicity
PRPH2-related disorder, PRPH2-related disorder
Health Risk
RS1582759492
Conflicting classifications of pathogenicity
Macular dystrophy, PRPH2-related disorder, Cone-rod dystrophy
Health Risk
RS1582764519
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Retinal dystrophy, PRPH2-related disorder
Health Risk
RS1761907993
Conflicting classifications of pathogenicity
Retinal dystrophy, PRPH2-related disorder, Retinal dystrophy
Health Risk
All Variants (309)
RSID Category Clinical Significance Conditions
RS2152011135 Health Risk Pathogenic PRPH2-related disorder, Retinal dystrophy, PRPH2-related disorder
RS2152011142 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2152011148 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548298268 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548298274 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548298312 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548298363 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548298397 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548300655 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548300670 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548300686 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548300727 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548300729 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548300782 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548300822 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548300838 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548309582 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548309605 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548309660 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548309705 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548309708 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548309755 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548309785 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548309835 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548309917 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS2548309957 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS281865372 Health Risk Pathogenic Pigmentary retinal dystrophy, PRPH2-related disorder, Pigmentary retinal dystrophy
RS281865373 Health Risk Pathogenic PRPH2-related disorder, Retinal dystrophy, Stargardt disease
RS281865374 Health Risk Pathogenic
RS281865375 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS535111150 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS61748429 Health Risk Pathogenic Patterned macular dystrophy 1, Retinal dystrophy, PRPH2-related disorder
RS61748433 Health Risk Pathogenic Retinitis pigmentosa 7, PRPH2-related disorder, Retinal dystrophy
RS61755765 Health Risk Pathogenic Retinitis punctata albescens, autosomal dominant, Retinitis punctata albescens
RS61755768 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS61755769 Health Risk Pathogenic Retinal dystrophy, Stargardt disease, PRPH2-related disorder
RS61755775 Health Risk Pathogenic PRPH2-related disorder, Choroidal dystrophy, central areolar 2
RS61755776 Health Risk Pathogenic Retinitis pigmentosa, PRPH2-related disorder, Retinitis pigmentosa
RS61755778 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS61755784 Health Risk Pathogenic maculopathy, Stargardt disease, PRPH2-related disorder
RS61755786 Health Risk Pathogenic Retinitis pigmentosa 7, Patterned macular dystrophy 1, Stargardt disease
RS61755797 Health Risk Pathogenic Vitelliform macular dystrophy 2, PRPH2-related disorder, PRPH2-related disorder
RS61755800 Health Risk Pathogenic Retinitis pigmentosa, PRPH2-related disorder, Retinal dystrophy
RS61755802 Health Risk Pathogenic Leber congenital amaurosis 18, Patterned macular dystrophy 1, PRPH2-related disorder
RS61755804 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS61755811 Health Risk Pathogenic Retinitis pigmentosa, Retinal dystrophy, PRPH2-related disorder
RS61755812 Health Risk Pathogenic
RS61755813 Health Risk Pathogenic Patterned macular dystrophy 1, Cone-rod dystrophy, Retinitis pigmentosa
RS61755814 Health Risk Pathogenic Macular dystrophy, Stargardt disease, PRPH2-related disorder
RS61755815 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
Sign Up to Analyze Your DNA Log In