Gene: RP1 ×
Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6101
Gene Symbol: RP1
RP1 		0.500 CausalMutation disease CLINVAR Impact of whole exome sequencing among Iranian patients with autosomal recessive retinitis pigmentosa. 26497376 2015
Entrez Id: 6101
Gene Symbol: RP1
RP1 		0.500 CausalMutation disease CLINVAR Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies. 24265693 2013
Entrez Id: 6101
Gene Symbol: RP1
RP1 		0.500 CausalMutation disease CLINVAR Three novel and the common Arg677Ter RP1 protein truncating mutations causing autosomal dominant retinitis pigmentosa in a Spanish population. 16597330 2006
Entrez Id: 6101
Gene Symbol: RP1
RP1 		0.500 CausalMutation disease CLINVAR RP1 protein truncating mutations predominate at the RP1 adRP locus. 11095597 2000
Entrez Id: 6101
Gene Symbol: RP1
RP1 		0.500 CausalMutation disease CLINVAR Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa. 10484783 1999
Entrez Id: 6101
Gene Symbol: RP1
RP1 		0.500 CausalMutation disease CLINVAR Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa. 10391211 1999
Entrez Id: 6101
Gene Symbol: RP1
RP1 		0.500 GeneticVariation disease CLINVAR