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
RS61755817 Health Risk Likely pathogenic Retinitis pigmentosa, Vitelliform macular dystrophy 3, Retinitis pigmentosa
RS62645932 Health Risk Likely pathogenic PRPH2-related disorder, PRPH2-related disorder
RS745427463 Health Risk Likely pathogenic
RS748478593 Health Risk Likely pathogenic Vitelliform macular dystrophy 3, Vitelliform macular dystrophy 3
RS749603273 Health Risk Likely pathogenic PRPH2-related disorder, Retinal dystrophy, PRPH2-related disorder
RS752610846 Health Risk Likely pathogenic PRPH2-related disorder, PRPH2-related disorder
RS753657349 Health Risk Likely pathogenic Macular dystrophy, PRPH2-related disorder, Retinitis pigmentosa 7
RS757988141 Health Risk Likely pathogenic PRPH2-related disorder, PRPH2-related disorder
RS777534414 Health Risk Likely pathogenic PRPH2-related disorder, PRPH2-related disorder
RS901479607 Health Risk Likely pathogenic PRPH2-related disorder, PRPH2-related disorder, PRPH2-related disorder
RS973931180 Health Risk Likely pathogenic PRPH2-related disorder, Retinal dystrophy, PRPH2-related disorder
RS1064793237 Health Risk Pathogenic Retinal dystrophy, Retinitis pigmentosa, PRPH2-related disorder
RS1203908646 Health Risk Pathogenic Patterned macular dystrophy 1, PRPH2-related disorder, Patterned macular dystrophy 1
RS121918564 Health Risk Pathogenic Vitelliform macular dystrophy 3, PRPH2-related disorder, Vitelliform macular dystrophy 3
RS121918565 Health Risk Pathogenic PRPH2-related disorder, Vitelliform macular dystrophy 3, Retinal dystrophy
RS121918566 Health Risk Pathogenic Vitelliform macular dystrophy 3, Vitelliform macular dystrophy 3
RS1377137374 Health Risk Pathogenic
RS1395223954 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS1426763534 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS1554268546 Health Risk Pathogenic Retinitis pigmentosa, PRPH2-related disorder, Retinitis pigmentosa
RS1554269053 Health Risk Pathogenic Retinal dystrophy, Retinitis pigmentosa, PRPH2-related disorder
RS1554269071 Health Risk Pathogenic Adult-onset foveomacular vitelliform dystrophy, PRPH2-related disorder, Adult-onset foveomacular vitelliform dystrophy
RS1554269081 Health Risk Pathogenic Retinitis pigmentosa, Retinal dystrophy, PRPH2-related disorder
RS1554270834 Health Risk Pathogenic Retinal dystrophy, Stargardt disease, PRPH2-related disorder
RS1562434117 Health Risk Pathogenic Adult-onset foveomacular vitelliform dystrophy, Adult-onset foveomacular vitelliform dystrophy
RS1582759785 Health Risk Pathogenic Patterned macular dystrophy 1, PRPH2-related disorder, Patterned macular dystrophy 1
RS1582764528 Health Risk Pathogenic Macular dystrophy, PRPH2-related disorder, Macular dystrophy
RS1582764765 Health Risk Pathogenic
RS1582764878 Health Risk Pathogenic Retinitis pigmentosa, PRPH2-related disorder, Retinitis pigmentosa
RS1761904690 Health Risk Pathogenic Retinal dystrophy, PRPH2-related disorder, PRPH2-related disorder
RS1761908297 Health Risk Pathogenic Retinitis pigmentosa, PRPH2-related disorder, Retinitis pigmentosa
RS1761908800 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS1761913253 Health Risk Pathogenic Stargardt disease, PRPH2-related disorder, Patterned dystrophy of the retinal pigment epithelium
RS1761913693 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS1761914145 Health Risk Pathogenic Central areolar choroidal dystrophy, Choroidal dystrophy, central areolar 2
RS1761915366 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS1761916286 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder, PRPH2-related disorder
RS1761917286 Health Risk Pathogenic Stargardt disease, PRPH2-related disorder, Stargardt disease
RS1761917626 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS1761921867 Health Risk Pathogenic PRPH2-related disorder, Retinal dystrophy, PRPH2-related disorder
RS1799986394 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS1799986608 Health Risk Pathogenic Retinal dystrophy, Vitelliform macular dystrophy 3, PRPH2-related disorder
RS1800108516 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder, PRPH2-related disorder
RS1800109348 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS1800110629 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS1800111025 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS1800113276 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS1800113541 Health Risk Pathogenic Cone dystrophy, Cone dystrophy
RS1800115217 Health Risk Pathogenic PRPH2-related disorder, PRPH2-related disorder
RS1800115811 Health Risk Pathogenic PRPH2-related disorder, Patterned dystrophy of the retinal pigment epithelium, PRPH2-related disorder
Sign Up to Analyze Your DNA Log In