Reviewed January 2013
What is the official name of the LRP5 gene?
The official name of this gene is “low density lipoprotein receptor-related protein 5.”
LRP5 is the gene's official symbol. The LRP5 gene is also known by other names, listed below.
What is the normal function of the LRP5 gene?
The LRP5 gene provides instructions for making a protein that is embedded in the outer membrane of many types of cells. It is known as a co-receptor because it works with another receptor protein, frizzled-4 (produced from the FZD4 gene), to transmit chemical signals from outside the cell to the cell's nucleus. Frizzled-4 and the LRP5 protein participate in the Wnt signaling pathway, a series of steps that affect the way cells and tissues develop. Wnt signaling is important for cell division (proliferation), attachment of cells to one another (adhesion), cell movement (migration), and many other cellular activities.
The LRP5 protein plays an important role in the development and maintenance of several tissues. During early development, it helps guide the specialization of cells in the retina, which is the light-sensitive tissue at the back of the eye. The LRP5 protein is also involved in establishing a blood supply to the retina and the inner ear. Additionally, this protein helps regulate bone mineral density, which is a measure of the amount of calcium and other minerals in bones. The minerals give the bones strength, making them less likely to break.
How are changes in the LRP5 gene related to health conditions?
- familial exudative vitreoretinopathy - caused by mutations in the LRP5 gene
More than 15 mutations in the LRP5 gene have been identified in people with the eye disease familial exudative vitreoretinopathy. Some of these mutations change single protein building blocks (amino acids) in the LRP5 protein, while others insert or delete genetic material in the gene. Most of these mutations reduce the amount of functional LRP5 protein that is produced within cells.
A reduction in the amount of LRP5 protein disrupts chemical signaling in the developing eye, which interferes with the formation of blood vessels at the edges of the retina. The resulting abnormal blood supply to this tissue can lead to retinal damage and vision loss. Because the LRP5 protein plays a role in bone formation, LRP5 gene mutations also cause reduced bone mineral density in some people with familial exudative vitreoretinopathy.
- juvenile primary osteoporosis - caused by mutations in the LRP5 gene
At least five LRP5 gene mutations have been found in people with juvenile primary osteoporosis. Individuals with this condition have low bone mineral density and thinning of the bones (osteoporosis) beginning in childhood. Osteoporosis causes the bones to be brittle and to break easily, which leads to multiple bone fractures. The LRP5 gene mutations that cause this condition result in an LRP5 protein that is unable to transmit chemical signals along the Wnt signaling pathway. The resulting reduction in signaling disrupts regulation of bone mineral density, leading to osteoporosis at a young age.
- osteoporosis-pseudoglioma syndrome - caused by mutations in the LRP5 gene
More than 40 LRP5 gene mutations that cause osteoporosis-pseudoglioma syndrome have been identified. Beginning in childhood, people with this condition have extremely low bone mineral density and osteoporosis, which leads to multiple bone fractures. Affected individuals also have eye abnormalities that cause vision impairment from birth or early infancy. Many LRP5 gene mutations that cause osteoporosis-pseudoglioma syndrome prevent cells from making any LRP5 protein. Other mutations change single amino acids in the LRP5 protein. These abnormal proteins cannot insert into the outer membrane of the cell, which makes them unable to perform their function. Loss of LRP5 protein function disrupts the chemical signaling pathways that are needed for the formation of bone and for normal retinal development, leading to the bone and eye abnormalities characteristic of osteoporosis-pseudoglioma syndrome. It is unclear why some LRP5 gene mutations affect eye development and others do not.
- other disorders - caused by mutations in the LRP5 gene
Studies suggest that changes in the LRP5 gene may influence the risk of developing osteoporosis in adulthood. Other genetic and environmental factors likely contribute to this common disorder.
Other LRP5 gene mutations cause disorders associated with an increase in bone mineral density. These include autosomal dominant osteopetrosis type 1 and autosomal dominant osteosclerosis. In some cases, these conditions can cause abnormal bone growth and related skeletal abnormalities. Rarely, affected individuals have hearing loss or circulation problems in the brain. Other people with increased bone mineral density do not have any associated health problems. The mutations responsible for increased bone mineral density syndromes overactivate the LRP5 protein, which increases Wnt signaling within cells and enhances bone formation.
Where is the LRP5 gene located?
Cytogenetic Location: 11q13.4
Molecular Location on chromosome 11: base pairs 68,312,608 to 68,449,274
The LRP5 gene is located on the long (q) arm of chromosome 11 at position 13.4.
More precisely, the LRP5 gene is located from base pair 68,312,608 to base pair 68,449,274 on chromosome 11.
See How do geneticists indicate the location of a gene? (http://ghr.nlm.nih.gov/handbook/howgeneswork/genelocation) in the Handbook.
Where can I find additional information about LRP5?
You and your healthcare professional may find the following resources about LRP5 helpful.
Educational resources - Information pages
- Developmental Biology (sixth edition, 2000): The Wnt signal transduction pathway (figure) (http://www.ncbi.nlm.nih.gov/books/NBK10043/?rendertype=figure&id=A1062)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases: Osteoporosis Overview (http://www.niams.nih.gov/Health_Info/Bone/Osteoporosis/default.asp)
- Gene Reviews - Clinical summary (http://www.ncbi.nlm.nih.gov/books/NBK1147)
Genetic Testing Registry - Repository of genetic test information
- GTR: Genetic tests for LRP5 (http://www.ncbi.nlm.nih.gov/gtr/tests/?term=4041%5Bgeneid%5D)
You may also be interested in these resources, which are designed for genetics professionals and researchers.
- PubMed - Recent literature (http://www.ncbi.nlm.nih.gov/pubmed?term=%28%28LRP5%5BTIAB%5D%29%20OR%20%28low%20density%20lipoprotein%20receptor-related%20protein%205%5BTIAB%5D%29%29%20AND%20%28%28Genes%5BMH%5D%29%20OR%20%28Genetic%20Phenomena%5BMH%5D%29%29%20AND%20english%5Bla%5D%20AND%20human%5Bmh%5D%20AND%20%22last%201800%20days%22%5Bdp%5D)
OMIM - Genetic disorder catalog
- BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1 (http://omim.org/entry/601884)
- ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT (http://omim.org/entry/144750)
- LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 5 (http://omim.org/entry/603506)
- OSTEOPETROSIS, AUTOSOMAL DOMINANT 1 (http://omim.org/entry/607634)
Research Resources - Tools for researchers
- Atlas of Genetics and Cytogenetics in Oncology and Haematology (http://atlasgeneticsoncology.org/Genes/LRP5ID44282ch11q13.html)
- GeneCards (http://www.genecards.org/cgi-bin/carddisp.pl?id_type=entrezgene&id=4041)
- HGNC Gene Family: Low density lipoprotein receptors (http://www.genenames.org/genefamilies/LDLR)
- HGNC Gene Symbol Report (http://www.genenames.org/cgi-bin/gene_symbol_report?q=data/hgnc_data.php&hgnc_id=6697)
- NCBI Gene (http://www.ncbi.nlm.nih.gov/gene/4041)
- The Wnt Homepage at Stanford University: LRP/Arrow (http://web.stanford.edu/~rnusse/lrp/LRP.html)
What other names do people use for the LRP5 gene or gene products?
- low density lipoprotein receptor-related protein 7
See How are genetic conditions and genes named? (http://ghr.nlm.nih.gov/handbook/mutationsanddisorders/naming) in the Handbook.
What glossary definitions help with understanding LRP5?
autosomal dominant ;
bone formation ;
bone mineral density ;
cell division ;
You may find definitions for these and many other terms in the Genetics Home Reference
- Ai M, Heeger S, Bartels CF, Schelling DK; Osteoporosis-Pseudoglioma Collaborative Group. Clinical and molecular findings in osteoporosis-pseudoglioma syndrome. Am J Hum Genet. 2005 Nov;77(5):741-53. Epub 2005 Sep 27. (http://www.ncbi.nlm.nih.gov/pubmed/16252235?dopt=Abstract)
- Balemans W, Van Hul W. The genetics of low-density lipoprotein receptor-related protein 5 in bone: a story of extremes. Endocrinology. 2007 Jun;148(6):2622-9. Epub 2007 Mar 29. Review. (http://www.ncbi.nlm.nih.gov/pubmed/17395706?dopt=Abstract)
- Boyden LM, Mao J, Belsky J, Mitzner L, Farhi A, Mitnick MA, Wu D, Insogna K, Lifton RP. High bone density due to a mutation in LDL-receptor-related protein 5. N Engl J Med. 2002 May 16;346(20):1513-21. (http://www.ncbi.nlm.nih.gov/pubmed/12015390?dopt=Abstract)
- Gong Y, Slee RB, Fukai N, Rawadi G, Roman-Roman S, Reginato AM, Wang H, Cundy T, Glorieux FH, Lev D, Zacharin M, Oexle K, Marcelino J, Suwairi W, Heeger S, Sabatakos G, Apte S, Adkins WN, Allgrove J, Arslan-Kirchner M, Batch JA, Beighton P, Black GC, Boles RG, Boon LM, Borrone C, Brunner HG, Carle GF, Dallapiccola B, De Paepe A, Floege B, Halfhide ML, Hall B, Hennekam RC, Hirose T, Jans A, Jüppner H, Kim CA, Keppler-Noreuil K, Kohlschuetter A, LaCombe D, Lambert M, Lemyre E, Letteboer T, Peltonen L, Ramesar RS, Romanengo M, Somer H, Steichen-Gersdorf E, Steinmann B, Sullivan B, Superti-Furga A, Swoboda W, van den Boogaard MJ, Van Hul W, Vikkula M, Votruba M, Zabel B, Garcia T, Baron R, Olsen BR, Warman ML; Osteoporosis-Pseudoglioma Syndrome Collaborative Group. LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development. Cell. 2001 Nov 16;107(4):513-23. (http://www.ncbi.nlm.nih.gov/pubmed/11719191?dopt=Abstract)
- Hartikka H, Mäkitie O, Männikkö M, Doria AS, Daneman A, Cole WG, Ala-Kokko L, Sochett EB. Heterozygous mutations in the LDL receptor-related protein 5 (LRP5) gene are associated with primary osteoporosis in children. J Bone Miner Res. 2005 May;20(5):783-9. Epub 2005 Jan 4. (http://www.ncbi.nlm.nih.gov/pubmed/15824851?dopt=Abstract)
- He X, Semenov M, Tamai K, Zeng X. LDL receptor-related proteins 5 and 6 in Wnt/beta-catenin signaling: arrows point the way. Development. 2004 Apr;131(8):1663-77. Review. (http://www.ncbi.nlm.nih.gov/pubmed/15084453?dopt=Abstract)
- Korvala J, Jüppner H, Mäkitie O, Sochett E, Schnabel D, Mora S, Bartels CF, Warman ML, Deraska D, Cole WG, Hartikka H, Ala-Kokko L, Männikkö M. Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity. BMC Med Genet. 2012 Apr 10;13:26. doi: 10.1186/1471-2350-13-26. (http://www.ncbi.nlm.nih.gov/pubmed/22487062?dopt=Abstract)
- Levasseur R, Lacombe D, de Vernejoul MC. LRP5 mutations in osteoporosis-pseudoglioma syndrome and high-bone-mass disorders. Joint Bone Spine. 2005 May;72(3):207-14. Review. (http://www.ncbi.nlm.nih.gov/pubmed/15850991?dopt=Abstract)
- Little RD, Carulli JP, Del Mastro RG, Dupuis J, Osborne M, Folz C, Manning SP, Swain PM, Zhao SC, Eustace B, Lappe MM, Spitzer L, Zweier S, Braunschweiger K, Benchekroun Y, Hu X, Adair R, Chee L, FitzGerald MG, Tulig C, Caruso A, Tzellas N, Bawa A, Franklin B, McGuire S, Nogues X, Gong G, Allen KM, Anisowicz A, Morales AJ, Lomedico PT, Recker SM, Van Eerdewegh P, Recker RR, Johnson ML. A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait. Am J Hum Genet. 2002 Jan;70(1):11-9. Epub 2001 Dec 3. (http://www.ncbi.nlm.nih.gov/pubmed/11741193?dopt=Abstract)
- Mizuguchi T, Furuta I, Watanabe Y, Tsukamoto K, Tomita H, Tsujihata M, Ohta T, Kishino T, Matsumoto N, Minakami H, Niikawa N, Yoshiura K. LRP5, low-density-lipoprotein-receptor-related protein 5, is a determinant for bone mineral density. J Hum Genet. 2004;49(2):80-6. Epub 2004 Jan 15. (http://www.ncbi.nlm.nih.gov/pubmed/14727154?dopt=Abstract)
- NCBI Gene (http://www.ncbi.nlm.nih.gov/gene/4041)
- Qin M, Hayashi H, Oshima K, Tahira T, Hayashi K, Kondo H. Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes. Hum Mutat. 2005 Aug;26(2):104-12. (http://www.ncbi.nlm.nih.gov/pubmed/15981244?dopt=Abstract)
- Qin M, Kondo H, Tahira T, Hayashi K. Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy. Hum Genet. 2008 Jan;122(6):615-23. Epub 2007 Oct 23. (http://www.ncbi.nlm.nih.gov/pubmed/17955262?dopt=Abstract)
- Toomes C, Bottomley HM, Jackson RM, Towns KV, Scott S, Mackey DA, Craig JE, Jiang L, Yang Z, Trembath R, Woodruff G, Gregory-Evans CY, Gregory-Evans K, Parker MJ, Black GC, Downey LM, Zhang K, Inglehearn CF. Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q. Am J Hum Genet. 2004 Apr;74(4):721-30. Epub 2004 Mar 11. (http://www.ncbi.nlm.nih.gov/pubmed/15024691?dopt=Abstract)
- van Meurs JB, Trikalinos TA, Ralston SH, Balcells S, Brandi ML, Brixen K, Kiel DP, Langdahl BL, Lips P, Ljunggren O, Lorenc R, Obermayer-Pietsch B, Ohlsson C, Pettersson U, Reid DM, Rousseau F, Scollen S, Van Hul W, Agueda L, Akesson K, Benevolenskaya LI, Ferrari SL, Hallmans G, Hofman A, Husted LB, Kruk M, Kaptoge S, Karasik D, Karlsson MK, Lorentzon M, Masi L, McGuigan FE, Mellström D, Mosekilde L, Nogues X, Pols HA, Reeve J, Renner W, Rivadeneira F, van Schoor NM, Weber K, Ioannidis JP, Uitterlinden AG; GENOMOS Study. Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis. JAMA. 2008 Mar 19;299(11):1277-90. doi: 10.1001/jama.299.11.1277. (http://www.ncbi.nlm.nih.gov/pubmed/18349089?dopt=Abstract)
- Van Wesenbeeck L, Cleiren E, Gram J, Beals RK, Bénichou O, Scopelliti D, Key L, Renton T, Bartels C, Gong Y, Warman ML, De Vernejoul MC, Bollerslev J, Van Hul W. Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density. Am J Hum Genet. 2003 Mar;72(3):763-71. Epub 2003 Feb 10. (http://www.ncbi.nlm.nih.gov/pubmed/12579474?dopt=Abstract)
The resources on this site should not be used as a substitute for
professional medical care or advice. Users seeking information about
a personal genetic disease, syndrome, or condition should consult with a qualified
See How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.