Gene: LRP5 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4041
Gene Symbol: LRP5
LRP5 		0.110 GeneticVariation disease BEFREE When the results of the exome and microarray data were considered together as a splice-site mutation in LRP5 gene [c.2827 + 1G > A], which is known to be important for eye development and Wnt receptor signaling pathway, was found to be the cause of microphthalmia in our family. 28111184 2017
Entrez Id: 4041
Gene Symbol: LRP5
LRP5 		0.110 Biomarker disease HPO