×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
Biomarker
disease
GENOMICS_ENGLAND
Novel Homozygous LRP5 Mutations in Mexican Patients with Osteoporosis-Pseudoglioma Syndrome.
29131652
2017
×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
GeneticVariation
disease
UNIPROT
Identification of two novel LRP5 mutations in families with familial exudative vitreoretinopathy.
24715757
2014
×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
GeneticVariation
disease
UNIPROT
Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP.
20340138
2010
×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
GeneticVariation
disease
UNIPROT
Clinical and molecular evaluation of probands and family members with familial exudative vitreoretinopathy.
19324841
2009
×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
GeneticVariation
disease
UNIPROT
Reduced bone mineral density and hyaloid vasculature remnants in a consanguineous recessive FEVR family with a mutation in LRP5.
16929062
2006
×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
GeneticVariation
disease
UNIPROT
Clinical and molecular findings in osteoporosis-pseudoglioma syndrome.
16252235
2005
×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
GeneticVariation
disease
UNIPROT
Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes.
15981244
2005
×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
GeneticVariation
disease
UNIPROT
Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.
15024691
2004
×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
GeneticVariation
disease
UNIPROT
Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5.
15346351
2004
×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
Biomarker
disease
GENOMICS_ENGLAND
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development.
11719191
2001
×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
CausalMutation
disease
CLINVAR
×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
Biomarker
disease
GENOMICS_ENGLAND
×
Entrez Id:
4041
Gene Symbol:
LRP5
LRP5
0.700
Biomarker
disease
CTD_human