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 		0.520 GeneticVariation disease UNIPROT Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy. 27228167 2016
Entrez Id: 4041
Gene Symbol: LRP5
LRP5 		0.520 GeneticVariation disease BEFREE Autosomal dominant FEVR (adFEVR), a major form of FEVR and assigned to chromosome 11q13-23 (EVR1) locus, is caused by deletion mutations in the C- terminal region of the frizzled-4 (FZD4) gene. 15370539 2004
Entrez Id: 4041
Gene Symbol: LRP5
LRP5 		0.520 GeneticVariation disease BEFREE This region contains LRP5 but not FZD4; mutations in both of these genes cause autosomal dominant FEVR. 15346351 2004
Entrez Id: 4041
Gene Symbol: LRP5
LRP5 		0.520 Biomarker disease CTD_human