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Genetics Home Reference: your guide to understanding genetic conditions
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CASR

Reviewed February 2015

What is the official name of the CASR gene?

The official name of this gene is “calcium-sensing receptor.”

CASR is the gene's official symbol. The CASR gene is also known by other names, listed below.

What is the normal function of the CASR gene?

The CASR gene provides instructions for making a protein called the calcium-sensing receptor (CaSR). Calcium molecules attach (bind) to CaSR, which allows this protein to monitor and regulate the amount of calcium in the blood. The receptor is turned on (activated) when a certain concentration of calcium is reached, and the activated receptor sends signals to block processes that increase the amount of calcium in the blood.

The CaSR protein is found in abundance in cells of the parathyroid glands. The parathyroid glands produce and release a hormone called parathyroid hormone that works to increase the levels of calcium in the blood. When large amounts of calcium bind to CaSR in the parathyroid glands, the production of parathyroid hormone is blocked, which prevents the release of more calcium into the blood. CaSR signaling also blocks the growth and division (proliferation) of cells that make up the parathyroid glands.

The CaSR protein is also found in kidney cells. Kidneys filter fluid and waste products in the body and can reabsorb needed nutrients and release them back into the blood. Increased calcium binding to CaSR in kidney cells blocks the reabsorption of calcium from the filtered fluids.

How are changes in the CASR gene related to health conditions?

autosomal dominant hypocalcemia - caused by mutations in the CASR gene

Mutations in the CASR gene can cause a condition called autosomal dominant hypocalcemia type 1, which is characterized by low levels of calcium in the blood (hypocalcemia). Some affected individuals also have a shortage of parathyroid hormone (hypoparathyroidism).

Most CASR gene mutations involved in this condition change single protein building blocks (amino acids) in the CaSR protein. The changes (called activating mutations) lead to an overactive CaSR that is more sensitive to calcium, meaning even low levels of calcium can trigger signaling. The overactive CaSR blocks the release of parathyroid hormone, which prevents the release of calcium into the blood. In addition, the overactive CaSR prevents reabsorption of calcium from the fluids filtered through the kidneys. Hypocalcemia can cause muscle cramping and seizures, although about half of people with this condition have no associated health problems.

familial isolated hyperparathyroidism - caused by mutations in the CASR gene

Mutations in the CASR gene have been found in some people with familial isolated hyperparathyroidism, a condition characterized by overactivity of the parathyroid glands (primary hyperparathyroidism). Primary hyperparathyroidism disrupts the normal balance of calcium in the blood, which can lead to kidney stones, thinning of the bones (osteoporosis), nausea, vomiting, high blood pressure (hypertension), weakness, and fatigue in people with familial isolated hyperparathyroidism. This condition is caused by changes to one copy of the gene in each cell. The CASR gene mutations associated with this condition change single amino acids in the CaSR protein. These genetic changes are called inactivating mutations because the altered CaSR protein is less sensitive to calcium and therefore requires an abnormally high concentration of calcium to trigger signaling. As a result, parathyroid hormone is produced even when the concentration of calcium in the blood is elevated, allowing the calcium levels to continue to rise. In addition, parathyroid cells may proliferate without control, which occasionally causes enlargement of the parathyroid glands in people with familial isolated hyperparathyroidism. Overproduction of parathyroid hormone from these abnormal glands may further stimulate the release of calcium into the blood. The high levels of calcium cause the signs and symptoms of familial isolated hyperparathyroidism.

Some researchers believe that familial isolated hyperparathyroidism caused by CASR gene mutations is a more severe form of a similar condition called familial hypocalciuric hypercalcemia (described below).

other disorders - caused by mutations in the CASR gene

Mutations in the CASR gene are involved in several other conditions associated with abnormal calcium levels. Inactivating mutations that lead to a reduction in CaSR function can cause familial hypocalciuric hypercalcemia. This condition is characterized by high levels of calcium in the blood (hypercalcemia) and low levels of calcium in the urine (hypocalciuria), but affected individuals typically have no symptoms related to the condition. Rarely, affected individuals have enlarged parathyroid glands and slightly elevated levels of parathyroid hormone. Like familial isolated hyperparathyroidism, this condition is caused by mutation of a single copy of the CASR gene.

A more serious condition called neonatal severe hyperparathyroidism is caused by genetic mutations that lead to very little or no CaSR function. In people with this condition, both copies of the CASR gene are altered. Neonatal severe hyperparathyroidism is a potentially fatal condition that becomes apparent in infants under the age of 6 months. Affected babies often have overgrowth of one or more of their parathyroid glands (parathyroid hyperplasia), causing high levels of parathyroid hormone in their blood. The excess hormone abnormally stimulates the release of calcium into the blood, causing hypercalcemia. The calcium is often removed from bone, resulting in skeletal abnormalities. The extreme hypercalcemia in these individuals can lead to neurological problems because the excess calcium interferes with nerve signaling.

Where is the CASR gene located?

Cytogenetic Location: 3q13

Molecular Location on chromosome 3: base pairs 122,183,666 to 122,286,502

The CASR gene is located on the long (q) arm of chromosome 3 at position 13.

The CASR gene is located on the long (q) arm of chromosome 3 at position 13.

More precisely, the CASR gene is located from base pair 122,183,666 to base pair 122,286,502 on chromosome 3.

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 CASR?

You and your healthcare professional may find the following resources about CASR helpful.

You may also be interested in these resources, which are designed for genetics professionals and researchers.

What other names do people use for the CASR gene or gene products?

  • CAR
  • extracellular calcium-sensing receptor
  • GPRC2A
  • parathyroid Ca(2+)-sensing receptor 1
  • parathyroid cell calcium-sensing receptor
  • PCAR1

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 CASR?

acids ; autosomal ; autosomal dominant ; Ca ; calcium ; cell ; extracellular ; familial ; gene ; hormone ; hypercalcemia ; hyperparathyroidism ; hyperplasia ; hypertension ; hypoparathyroidism ; kidney ; kidney stones ; mutation ; neonatal ; neurological ; osteoporosis ; parathyroid ; proliferate ; proliferation ; protein ; receptor

You may find definitions for these and many other terms in the Genetics Home Reference Glossary.

References

  • OMIM: CALCIUM-SENSING RECEPTOR (http://omim.org/entry/601199)
  • Carling T, Szabo E, Bai M, Ridefelt P, Westin G, Gustavsson P, Trivedi S, Hellman P, Brown EM, Dahl N, Rastad J. Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor. J Clin Endocrinol Metab. 2000 May;85(5):2042-7. (http://www.ncbi.nlm.nih.gov/pubmed/10843194?dopt=Abstract)
  • Hannan FM, Nesbit MA, Christie PT, Lissens W, Van der Schueren B, Bex M, Bouillon R, Thakker RV. A homozygous inactivating calcium-sensing receptor mutation, Pro339Thr, is associated with isolated primary hyperparathyroidism: correlation between location of mutations and severity of hypercalcaemia. Clin Endocrinol (Oxf). 2010 Dec;73(6):715-22. doi: 10.1111/j.1365-2265.2010.03870.x. (http://www.ncbi.nlm.nih.gov/pubmed/20846291?dopt=Abstract)
  • Hendy GN, Guarnieri V, Canaff L. Calcium-sensing receptor and associated diseases. Prog Mol Biol Transl Sci. 2009;89:31-95. doi: 10.1016/S1877-1173(09)89003-0. Epub 2009 Oct 7. Review. (http://www.ncbi.nlm.nih.gov/pubmed/20374733?dopt=Abstract)
  • Kinoshita Y, Hori M, Taguchi M, Watanabe S, Fukumoto S. Functional activities of mutant calcium-sensing receptors determine clinical presentations in patients with autosomal dominant hypocalcemia. J Clin Endocrinol Metab. 2014 Feb;99(2):E363-8. doi: 10.1210/jc.2013-3430. Epub 2013 Dec 2. (http://www.ncbi.nlm.nih.gov/pubmed/24297799?dopt=Abstract)
  • NCBI Gene (http://www.ncbi.nlm.nih.gov/gene/846)
  • Ranieri M, Tamma G, Di Mise A, Vezzoli G, Soldati L, Svelto M, Valenti G. Excessive signal transduction of gain-of-function variants of the calcium-sensing receptor (CaSR) are associated with increased ER to cytosol calcium gradient. PLoS One. 2013 Nov 14;8(11):e79113. doi: 10.1371/journal.pone.0079113. eCollection 2013. (http://www.ncbi.nlm.nih.gov/pubmed/24244430?dopt=Abstract)
  • Raue F, Pichl J, Dörr HG, Schnabel D, Heidemann P, Hammersen G, Jaursch-Hancke C, Santen R, Schöfl C, Wabitsch M, Haag C, Schulze E, Frank-Raue K. Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey. Clin Endocrinol (Oxf). 2011 Dec;75(6):760-5. doi: 10.1111/j.1365-2265.2011.04142.x. (http://www.ncbi.nlm.nih.gov/pubmed/21645025?dopt=Abstract)
  • Thim SB, Birkebaek NH, Nissen PH, Høst C. Activating calcium-sensing receptor gene variants in children: a case study of infant hypocalcaemia and literature review. Acta Paediatr. 2014 Jul 10. doi: 10.1111/apa.12743. [Epub ahead of print]. (http://www.ncbi.nlm.nih.gov/pubmed/25039540?dopt=Abstract)
  • Warner J, Epstein M, Sweet A, Singh D, Burgess J, Stranks S, Hill P, Perry-Keene D, Learoyd D, Robinson B, Birdsey P, Mackenzie E, Teh BT, Prins JB, Cardinal J. Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications. J Med Genet. 2004 Mar;41(3):155-60. (http://www.ncbi.nlm.nih.gov/pubmed/14985373?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 healthcare professional. See How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.

 
Reviewed: February 2015
Published: July 27, 2015