ITPR2 Chromosome 12

Inositol 1,4,5-trisphosphate receptor type 2
3 variants 3 Health Risk

Upload your DNA to see your personal genotypes for variants in ITPR2.

What This Gene Does
The protein encoded by this gene belongs to the inositol 1,4,5-triphosphate receptor family, whose members are second messenger intracellular calcium release channels. These proteins mediate a rise in cytoplasmic calcium in response to receptor activated production of inositol triphosphate. Inositol triphosphate receptor-mediated signaling is involved in many processes including cell migration, cell division, smooth muscle contraction, and neuronal signaling. This protein is a type 2 receptor that consists of a cytoplasmic amino-terminus that binds inositol triphosphate, six membrane-spanning helices that contribute to the ion pore, and a short cytoplasmic carboxy-terminus. A mutation in this gene has been associated with anhidrosis, suggesting that intracellular calcium release mediated by this protein is required for eccrine sweat production. [provided by RefSeq, Apr 2015]
Gene Info
Gene Group
"Inositol 1,4,5-triphosphate receptors|Cilia and flagella associated"
Locus Type
gene with protein product
Location
12p11.23
Ensembl
ENSG00000123104
Associated Conditions (2)
ITPR2-related disorder
Isolated anhidrosis with normal sweat glands
Key Variants
All Variants (3)
RSID Category Clinical Significance Conditions
RS200346963 Health Risk Conflicting classifications of pathogenicity ITPR2-related disorder, ITPR2-related disorder
RS202218048 Health Risk Conflicting classifications of pathogenicity ITPR2-related disorder, ITPR2-related disorder
RS786204832 Health Risk Pathogenic Isolated anhidrosis with normal sweat glands, Isolated anhidrosis with normal sweat glands
Sign Up to Analyze Your DNA Log In