Gene: PRPF31 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26121
Gene Symbol: PRPF31
PRPF31 		0.120 GeneticVariation phenotype BEFREE Heterozygous mutations in the PRPF31 gene cause autosomal dominant retinitis pigmentosa (adRP), a hereditary disorder leading to progressive blindness. 23144630 2012
Entrez Id: 26121
Gene Symbol: PRPF31
PRPF31 		0.120 GeneticVariation phenotype BEFREE Mutations in PRPF31 have been implicated in autosomal dominant retinitis pigmentosa (adRP), a frequent and important cause of blindness worldwide. 22723017 2012
Entrez Id: 26121
Gene Symbol: PRPF31
PRPF31 		0.120 Biomarker phenotype HPO