PDE6B Chromosome 4

Phosphodiesterase 6B
226 variants 226 Health Risk

Upload your DNA to see your personal genotypes for variants in PDE6B.

What This Gene Does
Photon absorption triggers a signaling cascade in rod photoreceptors that activates cGMP phosphodiesterase (PDE), resulting in the rapid hydrolysis of cGMP, closure of cGMP-gated cation channels, and hyperpolarization of the cell. PDE is a peripheral membrane heterotrimeric enzyme made up of alpha, beta, and gamma subunits. This gene encodes the beta subunit. Mutations in this gene result in retinitis pigmentosa and autosomal dominant congenital stationary night blindness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]
Gene Info
Gene Group
Phosphodiesterases
Locus Type
gene with protein product
Location
4p16.3
Ensembl
ENSG00000133256
Associated Conditions (19)
Retinitis pigmentosa
Congenital stationary night blindness autosomal dominant 2
Retinal dystrophy
Inborn genetic diseases
PDE6B-related disorder
Retinitis pigmentosa 40
Clear cell carcinoma of kidney
High myopia
Autosomal recessive retinitis pigmentosa
Progressive cone dystrophy (without rod involvement)
Rod-cone dystrophy
See cases
Cone-rod dystrophy
Thyroid cancer
nonmedullary
1
Leber congenital amaurosis
Congenital Stationary Night Blindness
Dominant
Key Variants
RS111504036
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Congenital stationary night blindness autosomal dominant 2, Retinitis pigmentosa
Health Risk
RS113246945
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Congenital stationary night blindness autosomal dominant 2, Retinal dystrophy
Health Risk
RS114100439
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Congenital stationary night blindness autosomal dominant 2, Retinitis pigmentosa
Health Risk
RS115775983
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Congenital stationary night blindness autosomal dominant 2, Retinal dystrophy
Health Risk
RS1302387853
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1305642045
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS138423108
Conflicting classifications of pathogenicity
Congenital stationary night blindness autosomal dominant 2, Retinitis pigmentosa, Retinal dystrophy
Health Risk
RS138682290
Conflicting classifications of pathogenicity
Congenital stationary night blindness autosomal dominant 2, Retinitis pigmentosa, Congenital stationary night blindness autosomal dominant 2
Health Risk
RS138789637
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Congenital stationary night blindness autosomal dominant 2, Retinitis pigmentosa
Health Risk
RS140224236
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Congenital stationary night blindness autosomal dominant 2, Retinal dystrophy
Health Risk
RS140441389
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS141647790
Conflicting classifications of pathogenicity
Congenital stationary night blindness autosomal dominant 2, Retinitis pigmentosa, Inborn genetic diseases
Health Risk
All Variants (226)
RSID Category Clinical Significance Conditions
RS1469569680 Health Risk Likely pathogenic
RS1470086286 Health Risk Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS1553810330 Health Risk Likely pathogenic
RS1553812554 Health Risk Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS1577296602 Health Risk Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS1734066308 Health Risk Likely pathogenic Retinitis pigmentosa 40, Retinitis pigmentosa 40
RS1734075026 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS1735848896 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS1736178477 Health Risk Likely pathogenic Autosomal recessive retinitis pigmentosa, Autosomal recessive retinitis pigmentosa
RS1736334634 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS1736402440 Health Risk Likely pathogenic Retinitis pigmentosa 40, Retinitis pigmentosa 40
RS2109207796 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS2109208075 Health Risk Likely pathogenic
RS2109284029 Health Risk Likely pathogenic Retinitis pigmentosa 40, Retinitis pigmentosa 40
RS2467360189 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS2474073903 Health Risk Likely pathogenic Congenital stationary night blindness autosomal dominant 2, Congenital stationary night blindness autosomal dominant 2
RS2474075677 Health Risk Likely pathogenic
RS2474104968 Health Risk Likely pathogenic
RS2474268824 Health Risk Likely pathogenic
RS2474268882 Health Risk Likely pathogenic
RS376325785 Health Risk Likely pathogenic Retinitis pigmentosa 40, Retinitis pigmentosa 40
RS527236089 Health Risk Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS527236090 Health Risk Likely pathogenic Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa
RS527236091 Health Risk Likely pathogenic Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa
RS536742386 Health Risk Likely pathogenic Progressive cone dystrophy (without rod involvement), Rod-cone dystrophy, Retinitis pigmentosa 40
RS746141070 Health Risk Likely pathogenic Retinitis pigmentosa 40, Retinal dystrophy, Retinitis pigmentosa 40
RS747684283 Health Risk Likely pathogenic Retinitis pigmentosa 40, Retinal dystrophy, Retinitis pigmentosa 40
RS751661904 Health Risk Likely pathogenic
RS753925314 Health Risk Likely pathogenic PDE6B-related disorder, Retinal dystrophy, PDE6B-related disorder
RS758052437 Health Risk Likely pathogenic Retinitis pigmentosa 40, Retinitis pigmentosa 40
RS761428338 Health Risk Likely pathogenic
RS761619791 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS766088717 Health Risk Likely pathogenic
RS769859376 Health Risk Likely pathogenic
RS776050413 Health Risk Likely pathogenic Retinitis pigmentosa 40, Retinitis pigmentosa 40
RS781003757 Health Risk Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa 40, Retinitis pigmentosa
RS934172185 Health Risk Likely pathogenic
RS934976363 Health Risk Likely pathogenic
RS1201231261 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS1212998897 Health Risk Pathogenic Retinitis pigmentosa 40, Retinitis pigmentosa 40
RS121918579 Health Risk Pathogenic Retinitis pigmentosa 40, Retinitis pigmentosa, Retinal dystrophy
RS121918580 Health Risk Pathogenic Retinitis pigmentosa 40, Retinitis pigmentosa 40
RS121918581 Health Risk Pathogenic Retinitis pigmentosa 40, Retinitis pigmentosa, Retinal dystrophy
RS121918582 Health Risk Pathogenic Congenital stationary night blindness autosomal dominant 2, Congenital stationary night blindness autosomal dominant 2
RS121918583 Health Risk Pathogenic Retinitis pigmentosa 40, Autosomal recessive retinitis pigmentosa, Retinal dystrophy
RS1325957874 Health Risk Pathogenic Retinitis pigmentosa 40, Congenital stationary night blindness autosomal dominant 2, Retinitis pigmentosa 40
RS1360000258 Health Risk Pathogenic
RS1360639709 Health Risk Pathogenic
RS1360937549 Health Risk Pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS1392709495 Health Risk Pathogenic Retinitis pigmentosa 40, Retinitis pigmentosa 40
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