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
RS764288902 Health Risk Conflicting classifications of pathogenicity 8 conditions, 8 conditions
RS764663599 Health Risk Conflicting classifications of pathogenicity
RS765468063 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS765952535 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, Osteogenesis imperfecta
RS766988509 Health Risk Conflicting classifications of pathogenicity
RS767509386 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS768638466 Health Risk Conflicting classifications of pathogenicity LRP5-related disorder, LRP5-related disorder
RS769128606 Health Risk Conflicting classifications of pathogenicity
RS770291326 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS773523178 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS774270653 Health Risk Conflicting classifications of pathogenicity Familial exudative vitreoretinopathy, Ovarian serous cystadenocarcinoma, Familial exudative vitreoretinopathy
RS776324795 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS776920568 Health Risk Conflicting classifications of pathogenicity LRP5-related disorder, LRP5-related disorder
RS778180589 Health Risk Conflicting classifications of pathogenicity
RS778998196 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS779935967 Health Risk Conflicting classifications of pathogenicity Osteoporosis with pseudoglioma, Inborn genetic diseases, 6 conditions
RS78219242 Health Risk Conflicting classifications of pathogenicity
RS80358306 Health Risk Conflicting classifications of pathogenicity LRP5-related disorder, Inborn genetic diseases, LRP5-related disorder
RS80358313 Health Risk Conflicting classifications of pathogenicity Exudative vitreoretinopathy 4, autosomal recessive, Retinal dystrophy
RS80358317 Health Risk Conflicting classifications of pathogenicity Exudative vitreoretinopathy 4, Osteogenesis imperfecta, LRP5-related disorder
RS80358320 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS867927445 Health Risk Conflicting classifications of pathogenicity
RS868085658 Health Risk Conflicting classifications of pathogenicity
RS956302502 Health Risk Conflicting classifications of pathogenicity
RS1057519127 Health Risk Likely pathogenic
RS1057519574 Health Risk Likely pathogenic Osteoporosis with pseudoglioma, Osteoporosis with pseudoglioma
RS1057519575 Health Risk Likely pathogenic Osteoporosis with pseudoglioma, Osteoporosis with pseudoglioma
RS121908668 Health Risk Likely pathogenic High bone mass, Disorder of bone, High bone mass
RS1229615060 Health Risk Likely pathogenic Osteoporosis with pseudoglioma, Osteoporosis with pseudoglioma
RS1270099780 Health Risk Likely pathogenic Osteoporosis with pseudoglioma, Osteoporosis with pseudoglioma
RS1281959115 Health Risk Likely pathogenic
RS141178995 Health Risk Likely pathogenic Polycystic liver disease 1, Polycystic liver disease 4 with or without kidney cysts, 6 conditions
RS1555075567 Health Risk Likely pathogenic High bone mass, High bone mass
RS1565083843 Health Risk Likely pathogenic Vitreoretinopathy, Retinal dystrophy, Vitreoretinopathy
RS1565347300 Health Risk Likely pathogenic
RS201093134 Health Risk Likely pathogenic
RS201745746 Health Risk Likely pathogenic Exudative vitreoretinopathy 4, Exudative vitreoretinopathy 4
RS2098629307 Health Risk Likely pathogenic
RS2098630548 Health Risk Likely pathogenic Exudative vitreoretinopathy 4, Exudative vitreoretinopathy 4
RS2098660903 Health Risk Likely pathogenic Exudative vitreoretinopathy 1, Exudative vitreoretinopathy 1
RS2098673363 Health Risk Likely pathogenic
RS2098675378 Health Risk Likely pathogenic
RS2098677149 Health Risk Likely pathogenic Exudative vitreoretinopathy 4, Exudative vitreoretinopathy 4
RS2153110244 Health Risk Likely pathogenic
RS2153140527 Health Risk Likely pathogenic Osteogenesis imperfecta, Osteogenesis imperfecta
RS2153153124 Health Risk Likely pathogenic Autosomal dominant polycystic liver disease, Autosomal dominant polycystic liver disease
RS2153167012 Health Risk Likely pathogenic
RS2153178673 Health Risk Likely pathogenic Exudative vitreoretinopathy 4, Exudative vitreoretinopathy 4
RS2496192280 Health Risk Likely pathogenic
RS2496385032 Health Risk Likely pathogenic Exudative vitreoretinopathy 4, Exudative vitreoretinopathy 4
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