LRP5 Chromosome 11

LDL receptor related protein 5
283 variants 283 Health Risk

Upload your DNA to see your personal genotypes for variants in LRP5.

What This Gene Does
This gene encodes a transmembrane low-density lipoprotein receptor that binds and internalizes ligands in the process of receptor-mediated endocytosis. This protein also acts as a co-receptor with Frizzled protein family members for transducing signals by Wnt proteins and was originally cloned on the basis of its association with type 1 diabetes mellitus in humans. This protein plays a key role in skeletal homeostasis and many bone density related diseases are caused by mutations in this gene. Mutations in this gene also cause familial exudative vitreoretinopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]
Gene Info
Gene Group
Low density lipoprotein receptors
Locus Type
gene with protein product
Location
11q13.2
Ensembl
ENSG00000162337
Associated Conditions (40)
Inborn genetic diseases
LRP5-related disorder
6 conditions
Osteoporosis with pseudoglioma
8 conditions
Osteogenesis imperfecta
Exudative vitreoretinopathy 4
autosomal recessive
Microcephaly
Retinal dystrophy
Uterine corpus endometrial carcinoma
Gastric cancer
Acute myeloid leukemia
Lung cancer
Cervical cancer
Polycystic kidney disease
adult type
Autosomal dominant polycystic liver disease
Clear cell carcinoma of kidney
Ovarian serous cystadenocarcinoma
+20 more conditions
Key Variants
All Variants (283)
RSID Category Clinical Significance Conditions
RS202149761 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS2098675372 Health Risk Conflicting classifications of pathogenicity
RS2496482483 Health Risk Conflicting classifications of pathogenicity Osteoporosis, Osteoporosis
RS2496598396 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS367543496 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS368178411 Health Risk Conflicting classifications of pathogenicity 8 conditions, 8 conditions
RS368198391 Health Risk Conflicting classifications of pathogenicity 8 conditions, 8 conditions
RS370347973 Health Risk Conflicting classifications of pathogenicity 8 conditions, 8 conditions
RS371514699 Health Risk Conflicting classifications of pathogenicity Polycystic liver disease 4 with or without kidney cysts, Polycystic liver disease 4 with or without kidney cysts
RS372126973 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS373910016 Health Risk Conflicting classifications of pathogenicity Polycystic liver disease 1, Polycystic liver disease 4 with or without kidney cysts, Osteogenesis imperfecta
RS376164225 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS376584791 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS377114189 Health Risk Conflicting classifications of pathogenicity
RS377145254 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS4988321 Health Risk Conflicting classifications of pathogenicity Osteoporosis with pseudoglioma, 8 conditions, Osteogenesis imperfecta
RS531205284 Health Risk Conflicting classifications of pathogenicity
RS536928726 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, Osteogenesis imperfecta
RS544861971 Health Risk Conflicting classifications of pathogenicity
RS555106014 Health Risk Conflicting classifications of pathogenicity LRP5-related disorder, 6 conditions, LRP5-related disorder
RS563657853 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS565245995 Health Risk Conflicting classifications of pathogenicity 8 conditions, 8 conditions
RS569392655 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS569517144 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, 8 conditions, LRP5-related disorder
RS569632869 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS61740517 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, 8 conditions, LRP5-related disorder
RS61889560 Health Risk Conflicting classifications of pathogenicity Polycystic kidney disease, adult type, 9 conditions
RS72555376 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, Osteogenesis imperfecta, Inborn genetic diseases
RS746800397 Health Risk Conflicting classifications of pathogenicity
RS747518922 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS748162115 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS748779058 Health Risk Conflicting classifications of pathogenicity 8 conditions, 8 conditions
RS749683290 Health Risk Conflicting classifications of pathogenicity
RS750573655 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, Osteogenesis imperfecta
RS752100031 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, LRP5-related disorder, Osteogenesis imperfecta
RS753598091 Health Risk Conflicting classifications of pathogenicity
RS754174678 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS755205426 Health Risk Conflicting classifications of pathogenicity
RS756103866 Health Risk Conflicting classifications of pathogenicity 8 conditions, 8 conditions
RS756825499 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, Osteogenesis imperfecta
RS756952499 Health Risk Conflicting classifications of pathogenicity Exudative vitreoretinopathy 4, Exudative vitreoretinopathy 4
RS757683069 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS757888034 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS759510890 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS760151423 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, Osteogenesis imperfecta
RS761049544 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS761245318 Health Risk Conflicting classifications of pathogenicity Exudative vitreoretinopathy 4, Exudative vitreoretinopathy 4
RS763601638 Health Risk Conflicting classifications of pathogenicity LRP5-related disorder, 6 conditions, LRP5-related disorder
RS763941232 Health Risk Conflicting classifications of pathogenicity
RS764138752 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, LRP5-related disorder, 6 conditions
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