rs112042188
This variant is located in the CASR gene.
▶ClinVar annotation
Autosomal dominant hypocalcemia 1; Familial hypocalciuric hypercalcemia 1; Neonatal severe primary hyperparathyroidism; Familial hypoparathyroidism; Familial hypocalciuric hypercalcemia;Autosomal dominant hypocalcemia 1; not specified; Hereditary cancer-predisposing syndrome; Nephrolithiasis/nephrocalcinosis; not provided
View on ClinVar →About CASR
The protein encoded by this gene is a plasma membrane G protein-coupled receptor that senses small changes in circulating calcium concentration. The encoded protein couples this information to intracellular signaling pathways that modify parathyroid hormone secretion or renal cation handling, and thus this protein plays an essential role in maintaining mineral ion homeostasis. Mutations in this gene are a cause of familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia. [provided by RefSeq, Aug 2017]
View all CASR variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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