CNGB1 Chromosome 16

Cyclic nucleotide gated channel subunit beta 1
229 variants 229 Health Risk

Upload your DNA to see your personal genotypes for variants in CNGB1.

What This Gene Does
In humans, the rod photoreceptor cGMP-gated cation channel helps regulate ion flow into the rod photoreceptor outer segment in response to light-induced alteration of the levels of intracellular cGMP. This channel consists of two subunits, alpha and beta, with the protein encoded by this gene representing the beta subunit. Defects in this gene are a cause of cause of retinitis pigmentosa type 45. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]
Gene Info
Gene Group
Cyclic nucleotide gated channels
Locus Type
gene with protein product
Location
16q21
Ensembl
ENSG00000070729
Associated Conditions (10)
Retinitis pigmentosa 45
Retinitis pigmentosa
Retinal dystrophy
Inborn genetic diseases
Optic atrophy
CNGB1-related disorder
CNGB1-related retinopathy
Autosomal recessive retinitis pigmentosa
See cases
Retinitis pigmentosa 49
Key Variants
All Variants (229)
RSID Category Clinical Significance Conditions
RS121918532 Health Risk Pathogenic Retinitis pigmentosa 45, Retinitis pigmentosa 45
RS1231250334 Health Risk Pathogenic Retinitis pigmentosa, Retinitis pigmentosa 45, Retinitis pigmentosa
RS1242363114 Health Risk Pathogenic
RS1304758484 Health Risk Pathogenic
RS1351453184 Health Risk Pathogenic
RS1352458826 Health Risk Pathogenic Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa 45
RS1420628245 Health Risk Pathogenic Retinitis pigmentosa, Retinitis pigmentosa 45, Retinitis pigmentosa
RS1451575280 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS1463251101 Health Risk Pathogenic
RS1567360969 Health Risk Pathogenic Retinitis pigmentosa 45, Retinitis pigmentosa 45
RS1567370223 Health Risk Pathogenic
RS1596976316 Health Risk Pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS1596997875 Health Risk Pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS1961354332 Health Risk Pathogenic
RS1961361358 Health Risk Pathogenic
RS1961604811 Health Risk Pathogenic
RS2149357361 Health Risk Pathogenic
RS2149358455 Health Risk Pathogenic Retinitis pigmentosa 45, Retinitis pigmentosa 45
RS2149358561 Health Risk Pathogenic
RS2149362043 Health Risk Pathogenic
RS2149364141 Health Risk Pathogenic
RS2149364812 Health Risk Pathogenic
RS2149364869 Health Risk Pathogenic
RS2149365820 Health Risk Pathogenic
RS2149366496 Health Risk Pathogenic
RS2149366536 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS2149372033 Health Risk Pathogenic Retinitis pigmentosa 45, Retinitis pigmentosa 45
RS2149388002 Health Risk Pathogenic
RS2149390170 Health Risk Pathogenic
RS2544628814 Health Risk Pathogenic
RS2544633550 Health Risk Pathogenic Retinitis pigmentosa 45, Retinitis pigmentosa 45
RS2544635088 Health Risk Pathogenic
RS2544655027 Health Risk Pathogenic
RS2544674147 Health Risk Pathogenic
RS2544678151 Health Risk Pathogenic
RS2544683005 Health Risk Pathogenic
RS367677784 Health Risk Pathogenic
RS367678786 Health Risk Pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS372504780 Health Risk Pathogenic Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa 45
RS530551814 Health Risk Pathogenic
RS753353134 Health Risk Pathogenic Retinal dystrophy, Retinitis pigmentosa 45, Retinal dystrophy
RS753776329 Health Risk Pathogenic Retinitis pigmentosa 45, Retinitis pigmentosa 45
RS754786301 Health Risk Pathogenic
RS755398007 Health Risk Pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS756885471 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS759380292 Health Risk Pathogenic
RS761839551 Health Risk Pathogenic Retinal dystrophy, Autosomal recessive retinitis pigmentosa, Retinal dystrophy
RS772049858 Health Risk Pathogenic
RS772200098 Health Risk Pathogenic
RS774264204 Health Risk Pathogenic Retinitis pigmentosa 45, Retinitis pigmentosa, See cases
Sign Up to Analyze Your DNA Log In