RLBP1 Chromosome 15

Retinaldehyde binding protein 1
63 variants 63 Health Risk

Upload your DNA to see your personal genotypes for variants in RLBP1.

What This Gene Does
The protein encoded by this gene is a 36-kD water-soluble protein which carries 11-cis-retinaldehyde or 11-cis-retinal as physiologic ligands. It may be a functional component of the visual cycle. Mutations of this gene have been associated with severe rod-cone dystrophy, Bothnia dystrophy (nonsyndromic autosomal recessive retinitis pigmentosa) and retinitis punctata albescens. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
CRAL-TRIO lipid binding domain containing
Locus Type
gene with protein product
Location
15q26.1
Ensembl
ENSG00000140522
Associated Conditions (11)
Newfoundland cone-rod dystrophy
Retinitis pigmentosa
Pigmentary retinal dystrophy
Bothnia retinal dystrophy
Retinal dystrophy
RLBP1-related disorder
Inborn genetic diseases
Retinitis punctata albescens
Autosomal recessive retinitis pigmentosa
Retinal disorder
Abnormality of the eye
Key Variants
RS1173705310
Conflicting classifications of pathogenicity
Newfoundland cone-rod dystrophy, Retinitis pigmentosa, Pigmentary retinal dystrophy
Health Risk
RS138965708
Conflicting classifications of pathogenicity
Pigmentary retinal dystrophy, Bothnia retinal dystrophy, Newfoundland cone-rod dystrophy
Health Risk
RS142244640
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Newfoundland cone-rod dystrophy, Pigmentary retinal dystrophy
Health Risk
RS143817941
Conflicting classifications of pathogenicity
Newfoundland cone-rod dystrophy, Pigmentary retinal dystrophy, Retinitis pigmentosa
Health Risk
RS144254383
Conflicting classifications of pathogenicity
Pigmentary retinal dystrophy, Retinitis pigmentosa, Newfoundland cone-rod dystrophy
Health Risk
RS144615495
Conflicting classifications of pathogenicity
Pigmentary retinal dystrophy, Newfoundland cone-rod dystrophy, Retinitis pigmentosa
Health Risk
RS144641995
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS146844731
Conflicting classifications of pathogenicity
RLBP1-related disorder, RLBP1-related disorder
Health Risk
RS150636501
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Pigmentary retinal dystrophy, Newfoundland cone-rod dystrophy
Health Risk
RS181321141
Conflicting classifications of pathogenicity
Newfoundland cone-rod dystrophy, Retinitis pigmentosa, Pigmentary retinal dystrophy
Health Risk
RS181863443
Conflicting classifications of pathogenicity
Newfoundland cone-rod dystrophy, Pigmentary retinal dystrophy, Retinitis pigmentosa
Health Risk
RS190236976
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Newfoundland cone-rod dystrophy, Pigmentary retinal dystrophy
Health Risk
All Variants (63)
RSID Category Clinical Significance Conditions
RS766278489 Health Risk Pathogenic Newfoundland cone-rod dystrophy, Retinitis punctata albescens, Retinitis pigmentosa
RS766675673 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS776260543 Health Risk Pathogenic Newfoundland cone-rod dystrophy, Pigmentary retinal dystrophy, Bothnia retinal dystrophy
RS137853291 Health Risk Pathogenic/Likely pathogenic Retinitis punctata albescens, RLBP1-related disorder, Retinitis pigmentosa
RS151141842 Health Risk Pathogenic/Likely pathogenic Pigmentary retinal dystrophy, Retinitis pigmentosa, Pigmentary retinal dystrophy
RS2051527389 Health Risk Pathogenic/Likely pathogenic Pigmentary retinal dystrophy, Newfoundland cone-rod dystrophy, Bothnia retinal dystrophy
RS28933990 Health Risk Pathogenic/Likely pathogenic Bothnia retinal dystrophy, Retinitis punctata albescens, RLBP1-related disorder
RS561618945 Health Risk Pathogenic/Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS759505780 Health Risk Pathogenic/Likely pathogenic Newfoundland cone-rod dystrophy, Pigmentary retinal dystrophy, Bothnia retinal dystrophy
RS760650165 Health Risk Pathogenic/Likely pathogenic RLBP1-related disorder, Newfoundland cone-rod dystrophy, Pigmentary retinal dystrophy
RS763694069 Health Risk Pathogenic/Likely pathogenic RLBP1-related disorder, Retinitis pigmentosa, RLBP1-related disorder
RS764825249 Health Risk Pathogenic/Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS786205626 Health Risk Pathogenic/Likely pathogenic Bothnia retinal dystrophy, Retinal dystrophy, Retinitis punctata albescens
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