Gene: SNRNP200 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23020
Gene Symbol: SNRNP200
SNRNP200 		0.700 GeneticVariation disease UNIPROT Mutations in the small nuclear riboprotein 200 kDa gene (SNRNP200) cause 1.6% of autosomal dominant retinitis pigmentosa. 24319334 2013
Entrez Id: 23020
Gene Symbol: SNRNP200
SNRNP200 		0.700 GeneticVariation disease UNIPROT Contribution of SNRNP200 sequence variations to retinitis pigmentosa. 23887765 2013
Entrez Id: 23020
Gene Symbol: SNRNP200
SNRNP200 		0.700 GeneticVariation disease UNIPROT A novel missense SNRNP200 mutation associated with autosomal dominant retinitis pigmentosa in a Chinese family. 23029027 2012
Entrez Id: 23020
Gene Symbol: SNRNP200
SNRNP200 		0.700 GeneticVariation disease UNIPROT Structural basis for functional cooperation between tandem helicase cassettes in Brr2-mediated remodeling of the spliceosome. 23045696 2012
Entrez Id: 23020
Gene Symbol: SNRNP200
SNRNP200 		0.700 GeneticVariation disease UNIPROT Next generation sequencing of pooled samples reveals new SNRNP200 mutations associated with retinitis pigmentosa. 21618346 2011
Entrez Id: 23020
Gene Symbol: SNRNP200
SNRNP200 		0.700 GeneticVariation disease UNIPROT Mutations in ASCC3L1 on 2q11.2 are associated with autosomal dominant retinitis pigmentosa in a Chinese family. 19710410 2010
Entrez Id: 23020
Gene Symbol: SNRNP200
SNRNP200 		0.700 GeneticVariation disease UNIPROT Autosomal-dominant retinitis pigmentosa caused by a mutation in SNRNP200, a gene required for unwinding of U4/U6 snRNAs. 19878916 2009
Entrez Id: 23020
Gene Symbol: SNRNP200
SNRNP200 		0.700 GeneticVariation disease UNIPROT The network of protein-protein interactions within the human U4/U6.U5 tri-snRNP. 16723661 2006
Entrez Id: 23020
Gene Symbol: SNRNP200
SNRNP200 		0.700 CausalMutation disease CLINVAR
Entrez Id: 23020
Gene Symbol: SNRNP200
SNRNP200 		0.700 Biomarker disease CTD_human
Entrez Id: 23020
Gene Symbol: SNRNP200
SNRNP200 		0.700 Biomarker disease GENOMICS_ENGLAND