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
RS1029914579 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS113315676 Health Risk Conflicting classifications of pathogenicity LRP5-related disorder, LRP5-related disorder
RS113804402 Health Risk Conflicting classifications of pathogenicity 6 conditions, LRP5-related disorder, 6 conditions
RS1158745675 Health Risk Conflicting classifications of pathogenicity Osteoporosis with pseudoglioma, Osteoporosis with pseudoglioma
RS1177481438 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS1197978360 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS1215728276 Health Risk Conflicting classifications of pathogenicity 8 conditions, 8 conditions
RS121908665 Health Risk Conflicting classifications of pathogenicity Osteoporosis with pseudoglioma, Osteogenesis imperfecta, Osteoporosis with pseudoglioma
RS121908674 Health Risk Conflicting classifications of pathogenicity Exudative vitreoretinopathy 4, autosomal recessive, Exudative vitreoretinopathy 4
RS1251382942 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS1273567061 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS1284857527 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS1326459816 Health Risk Conflicting classifications of pathogenicity Osteoporosis with pseudoglioma, Osteoporosis with pseudoglioma
RS1394646742 Health Risk Conflicting classifications of pathogenicity
RS140977837 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, LRP5-related disorder, Osteogenesis imperfecta
RS141407040 Health Risk Conflicting classifications of pathogenicity Microcephaly, Osteoporosis with pseudoglioma, Microcephaly
RS141889567 Health Risk Conflicting classifications of pathogenicity Osteoporosis with pseudoglioma, LRP5-related disorder, Retinal dystrophy
RS142506263 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS142508112 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, Inborn genetic diseases, Osteogenesis imperfecta
RS143396225 Health Risk Conflicting classifications of pathogenicity Polycystic kidney disease, adult type, LRP5-related disorder
RS143499301 Health Risk Conflicting classifications of pathogenicity LRP5-related disorder, LRP5-related disorder
RS143539498 Health Risk Conflicting classifications of pathogenicity Autosomal dominant polycystic liver disease, Inborn genetic diseases, Autosomal dominant polycystic liver disease
RS143878170 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS144983823 Health Risk Conflicting classifications of pathogenicity
RS145226802 Health Risk Conflicting classifications of pathogenicity LRP5-related disorder, LRP5-related disorder
RS145362529 Health Risk Conflicting classifications of pathogenicity LRP5-related disorder, LRP5-related disorder
RS145750689 Health Risk Conflicting classifications of pathogenicity LRP5-related disorder, LRP5-related disorder
RS146388120 Health Risk Conflicting classifications of pathogenicity
RS146667935 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, Osteogenesis imperfecta
RS147618989 Health Risk Conflicting classifications of pathogenicity Exudative vitreoretinopathy 4, Exudative vitreoretinopathy 4
RS147637431 Health Risk Conflicting classifications of pathogenicity
RS148550774 Health Risk Conflicting classifications of pathogenicity Clear cell carcinoma of kidney, Ovarian serous cystadenocarcinoma, Cervical cancer
RS148603249 Health Risk Conflicting classifications of pathogenicity
RS149166384 Health Risk Conflicting classifications of pathogenicity 8 conditions, LRP5-related disorder, 8 conditions
RS149241739 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS149524398 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, Osteogenesis imperfecta
RS150088620 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS150771999 Health Risk Conflicting classifications of pathogenicity LRP5-related disorder, 6 conditions, LRP5-related disorder
RS150859573 Health Risk Conflicting classifications of pathogenicity
RS1565308833 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS180941579 Health Risk Conflicting classifications of pathogenicity Microcephaly, 6 conditions, LRP5-related disorder
RS183377804 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS199871539 Health Risk Conflicting classifications of pathogenicity 8 conditions, LRP5-related disorder, 8 conditions
RS200389686 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS200409162 Health Risk Conflicting classifications of pathogenicity 8 conditions, Inborn genetic diseases, 8 conditions
RS200624778 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS201018263 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, Severe early-childhood-onset retinal dystrophy, Osteogenesis imperfecta
RS201030241 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, Osteogenesis imperfecta
RS201475647 Health Risk Conflicting classifications of pathogenicity
RS202067798 Health Risk Conflicting classifications of pathogenicity Osteogenesis imperfecta, Osteogenesis imperfecta
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