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 		0.500 CausalMutation disease CLINVAR Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q. 15024691 2004
Entrez Id: 4041
Gene Symbol: LRP5
LRP5 		0.500 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 		0.500 GeneticVariation disease BEFREE Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q. 15024691 2004
Entrez Id: 4041
Gene Symbol: LRP5
LRP5 		0.500 GeneticVariation disease BEFREE Loci associated with FEVR map to 11q13-q23 (EVR1; OMIM 133780, ref.1), Xp11.4 (EVR2; OMIM 305390, ref. 12172548 2002
Entrez Id: 4041
Gene Symbol: LRP5
LRP5 		0.500 GeneticVariation disease BEFREE Genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of the EVR1 locus on chromosome 11q in a large autosomal dominant pedigree. 10729291 2000