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JPH3

Gene

junctophilin 3

HGNCHGNC:14203EnsemblENSG00000154118NCBI Gene57338
Locus: gene with protein productLocation: 16q24.2

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asTNRC22 · JP-3 · CAGL237 · HDL2 · JP3
View full nomenclature history (7)
Previous symbolsTNRC22
Alias symbolsJP-3, CAGL237, HDL2, JP3
Previous namestrinucleotide repeat containing 22
Alias namesjunctophilin3

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Cardiomyopathy, Hypertrophic
Migraine Disorders
Kidney transplant
Genetic Diseases, Inborn
Blindness
Obesity disorder
Protozoan Infections

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Junctophilins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-08-10.
Open TargetsGene–disease associations from the Open Targets Platform.