TRPC4AP

Gene

transient receptor potential cation channel subfamily C member 4 associated protein

HGNCHGNC:16181 EnsemblENSG00000100991 NCBI Gene26133

Locus: gene with protein productLocation: 20q11.22

Also known as

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

Also known asC20orf188 · DKFZp586C1223 · dJ756N5.2 · TRRP4AP · PPP1R158 · DKFZP727M231

View full nomenclature history (9)

Previous symbolsC20orf188

Alias symbolsDKFZp586C1223, dJ756N5.2, TRRP4AP, PPP1R158, DKFZP727M231

Previous nameschromosome 20 open reading frame 188, transient receptor potential cation channel, subfamily C, member 4 associated protein

Alias namesprotein phosphatase 1, regulatory subunit 158

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.

Hypertrophic cardiomyopathy 1

Rare familial disorder with hypertrophic cardiomyopathy

Venous Thrombosis

Heart Diseases

Cardiomyopathy, Hypertrophic

Pulmonary Embolism

Skin Neoplasms

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.

Protein phosphatase 1 regulatory subunitsArmadillo like helical domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.