SNRNP200 Chromosome 2

Small nuclear ribonucleoprotein U5 subunit 200
95 variants 95 Health Risk

Upload your DNA to see your personal genotypes for variants in SNRNP200.

What This Gene Does
Pre-mRNA splicing is catalyzed by the spliceosome, a complex of specialized RNA and protein subunits that removes introns from a transcribed pre-mRNA segment. The spliceosome consists of small nuclear RNA proteins (snRNPs) U1, U2, U4, U5 and U6, together with approximately 80 conserved proteins. U5 snRNP contains nine specific proteins. This gene encodes one of the U5 snRNP-specific proteins. This protein belongs to the DEXH-box family of putative RNA helicases. It is a core component of U4/U6-U5 snRNPs and appears to catalyze an ATP-dependent unwinding of U4/U6 RNA duplices. Mutations in this gene cause autosomal-dominant retinitis pigmentosa. Alternatively spliced transcript variants encoding different isoforms have been found, but the full-length nature of these variants has not been determined. [provided by RefSeq, Mar 2010]
Gene Info
Gene Group
"U5 small nuclear ribonucleoprotein|Spliceosomal Bact complex|Spliceosomal C complex|Spliceosomal P complex"
Locus Type
gene with protein product
Location
2q11.2
Ensembl
ENSG00000144028
Associated Conditions (9)
Retinitis pigmentosa
Inborn genetic diseases
SNRNP200-related disorder
Retinal dystrophy
Retinitis pigmentosa 33
SNRNP200-related retinal disorder
Cervical cancer
Autosomal dominant retinitis pigmentosa
Retinal disorder
Key Variants
All Variants (95)
RSID Category Clinical Significance Conditions
RS1004264460 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS1057519143 Health Risk Conflicting classifications of pathogenicity
RS1295558388 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS1377252379 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS138291954 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS138992215 Health Risk Conflicting classifications of pathogenicity SNRNP200-related disorder, SNRNP200-related disorder
RS139137932 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS139286118 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS140087655 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS140629902 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, SNRNP200-related disorder, Retinitis pigmentosa
RS140702204 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS142585893 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS143175658 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS1437130482 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS144423660 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS144934076 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS145242546 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS145559167 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS147219591 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS148170370 Health Risk Conflicting classifications of pathogenicity
RS1573992736 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS1574001405 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS191245006 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS191776366 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS199736893 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa
RS200426430 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 33, Retinal dystrophy, Retinitis pigmentosa 33
RS200824314 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS201143866 Health Risk Conflicting classifications of pathogenicity
RS201501591 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS202243080 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, SNRNP200-related disorder, Retinitis pigmentosa
RS2063866129 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS2063912153 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS2063918355 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 33, SNRNP200-related disorder, Retinitis pigmentosa 33
RS367922991 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinitis pigmentosa 33, SNRNP200-related retinal disorder
RS368225080 Health Risk Conflicting classifications of pathogenicity SNRNP200-related disorder, SNRNP200-related disorder
RS370694903 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS371511825 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS372772120 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinitis pigmentosa 33, Retinal dystrophy
RS372940792 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS373701482 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS375650263 Health Risk Conflicting classifications of pathogenicity
RS375734152 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS376352502 Health Risk Conflicting classifications of pathogenicity
RS377631478 Health Risk Conflicting classifications of pathogenicity
RS377641548 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, SNRNP200-related disorder, Retinitis pigmentosa
RS397514574 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 33, Retinal dystrophy, Retinitis pigmentosa 33
RS527236115 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa
RS536493402 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Inborn genetic diseases, Retinal dystrophy
RS566448118 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS61753580 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
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