JPH3 Chromosome 16

Junctophilin 3
3 variants 3 Health Risk

Upload your DNA to see your personal genotypes for variants in JPH3.

What This Gene Does
Junctional complexes between the plasma membrane and endoplasmic/sarcoplasmic reticulum are a common feature of all excitable cell types and mediate cross talk between cell surface and intracellular ion channels. The protein encoded by this gene is a component of junctional complexes and is composed of a C-terminal hydrophobic segment spanning the endoplasmic/sarcoplasmic reticulum membrane and a remaining cytoplasmic domain that shows specific affinity for the plasma membrane. CAG/CTG repeat expansion from normally 6-28 repeats to 40-59 repeats in the 3' UTR of this gene have been associated with Huntington disease-like 2 (HDL2). This gene is a member of the junctophilin gene family. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Jul 2016]
Gene Info
Gene Group
Junctophilins
Locus Type
gene with protein product
Location
16q24.2
Ensembl
ENSG00000154118
Associated Conditions (3)
Inborn genetic diseases
Huntington disease-like 2
JPH3-related disorder
Key Variants
All Variants (3)
RSID Category Clinical Significance Conditions
RS142120839 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS144296512 Health Risk Conflicting classifications of pathogenicity Huntington disease-like 2, JPH3-related disorder, Huntington disease-like 2
RS200986386 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
Sign Up to Analyze Your DNA Log In