Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 115861
Gene Symbol: NXNL1
NXNL1
0.040 GeneticVariation disease BEFREE Moreover, a missense mutation of RdCVF results in its inability to bind to BSG1, stimulate glucose uptake, and prevent secondary cone death in a model of RP. 25957687 2015
Entrez Id: 115861
Gene Symbol: NXNL1
NXNL1
0.040 AlteredExpression disease 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
0.040 Biomarker disease BEFREE The demonstration at the functional level of the therapeutic potential of RdCVF in the most frequent of dominant RP mutations paves the way toward the use of RdCVF for preserving central vision in many RP patients. 19277021 2009
Entrez Id: 115861
Gene Symbol: NXNL1
NXNL1
0.040 Biomarker disease LHGDN Identification and characterization of rod-derived cone viability factor. 15220920 2004