JPH3 Chromosome 16
Junctophilin 3
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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
RS142120839
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS144296512
Conflicting classifications of pathogenicity
Huntington disease-like 2, JPH3-related disorder, Huntington disease-like 2
Health Risk
RS200986386
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
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 |