Gene: LRP4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4038
Gene Symbol: LRP4
LRP4 		0.500 GermlineCausalMutation disease ORPHANET LRP4 third β-propeller domain mutations cause novel congenital myasthenia by compromising agrin-mediated MuSK signaling in a position-specific manner. 24234652 2014
Entrez Id: 4038
Gene Symbol: LRP4
LRP4 		0.500 Biomarker disease CTD_human