Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Autosomal dominant retinitis pigmentosa
0.020 GeneticVariation disease BEFREE A missense mutation in PRPF6 causes impairment of pre-mRNA splicing and autosomal-dominant retinitis pigmentosa. 21549338 2011
Autosomal dominant retinitis pigmentosa
0.020 GeneticVariation disease BEFREE We identify 112 candidate ciliogenesis and ciliopathy genes, including 44 components of the ubiquitin-proteasome system, 12 G-protein-coupled receptors, and 3 pre-mRNA processing factors (PRPF6, PRPF8 and PRPF31) mutated in autosomal dominant retinitis pigmentosa. 26167768 2015