PRPF31 Chromosome 19

Pre-mRNA processing factor 31
222 variants 222 Health Risk

Upload your DNA to see your personal genotypes for variants in PRPF31.

What This Gene Does
This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]
Gene Info
Gene Group
U4/U6 small nuclear ribonucleoprotein particle
Locus Type
gene with protein product
Location
19q13.42
Ensembl
ENSG00000105618
Associated Conditions (7)
Retinal dystrophy
Retinitis pigmentosa
PRPF31-related disorder
Retinitis pigmentosa 11
Inborn genetic diseases
Retinal disorder
See cases
Key Variants
All Variants (222)
RSID Category Clinical Significance Conditions
RS2146418714 Health Risk Pathogenic
RS2146420160 Health Risk Pathogenic Retinitis pigmentosa 11, Retinal dystrophy, Retinitis pigmentosa 11
RS2146420442 Health Risk Pathogenic
RS2146420461 Health Risk Pathogenic
RS2146420616 Health Risk Pathogenic
RS2146420831 Health Risk Pathogenic
RS2146421194 Health Risk Pathogenic
RS2146421348 Health Risk Pathogenic
RS2146425748 Health Risk Pathogenic
RS2146425937 Health Risk Pathogenic
RS2146436261 Health Risk Pathogenic
RS2146436400 Health Risk Pathogenic Retinitis pigmentosa 11, Retinitis pigmentosa 11
RS2146436884 Health Risk Pathogenic
RS2146444340 Health Risk Pathogenic
RS2146445734 Health Risk Pathogenic
RS2146445759 Health Risk Pathogenic
RS2146445800 Health Risk Pathogenic
RS2146449761 Health Risk Pathogenic
RS2146449768 Health Risk Pathogenic
RS2146449804 Health Risk Pathogenic
RS2146449983 Health Risk Pathogenic
RS2146450050 Health Risk Pathogenic
RS2146450184 Health Risk Pathogenic
RS2516077994 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS2516083955 Health Risk Pathogenic
RS2516084081 Health Risk Pathogenic
RS2516116135 Health Risk Pathogenic
RS2516116438 Health Risk Pathogenic
RS2516117809 Health Risk Pathogenic
RS2516126445 Health Risk Pathogenic
RS2516145631 Health Risk Pathogenic
RS2516156843 Health Risk Pathogenic
RS2516157956 Health Risk Pathogenic
RS2516158518 Health Risk Pathogenic
RS2516158865 Health Risk Pathogenic Retinitis pigmentosa 11, Retinal dystrophy, Retinitis pigmentosa 11
RS2516177530 Health Risk Pathogenic
RS2516197396 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS2516204990 Health Risk Pathogenic
RS2516205141 Health Risk Pathogenic
RS2516205278 Health Risk Pathogenic
RS2516206256 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS2516206372 Health Risk Pathogenic
RS2516206637 Health Risk Pathogenic PRPF31-related disorder, PRPF31-related disorder
RS2516208014 Health Risk Pathogenic
RS587776589 Health Risk Pathogenic Retinitis pigmentosa 11, Retinitis pigmentosa 11
RS587776591 Health Risk Pathogenic Retinitis pigmentosa 11, Retinitis pigmentosa 11
RS727504107 Health Risk Pathogenic
RS779270349 Health Risk Pathogenic Retinal dystrophy, Retinitis pigmentosa 11, Retinal dystrophy
RS869312187 Health Risk Pathogenic Retinal dystrophy, Retinitis pigmentosa 11, Retinal dystrophy
RS1342475527 Health Risk Pathogenic/Likely pathogenic Retinal dystrophy, Retinitis pigmentosa 11, Retinal dystrophy
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