Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 115861
Gene Symbol: NXNL1
NXNL1
0.030 Biomarker phenotype BEFREE Because the secondary loss of cones in retinitis pigmentosa (RP) leads to blindness, the administration of RdCVF is a promising therapy for this untreatable neurodegenerative disease. 25957687 2015
Entrez Id: 115861
Gene Symbol: NXNL1
NXNL1
0.030 AlteredExpression phenotype BEFREE Based upon these results, we propose an alternative therapeutic strategy aimed at recapitulating RdCVF expression in the inner retina, where cell loss is not significant, to prevent secondary cone death and central vision loss in patients suffering from retinitis pigmentosa. 19843539 2010
Entrez Id: 115861
Gene Symbol: NXNL1
NXNL1
0.030 GeneticVariation phenotype LHGDN Disease-associated variants of the rod-derived cone viability factor (RdCVF) in Leber congenital amaurosis. Rod-derived cone viability variants in LCA. 17249548 2006