TRIP4

Gene

thyroid hormone receptor interactor 4

HGNCHGNC:12310 EnsemblENSG00000103671 NCBI Gene9325

Locus: gene with protein productLocation: 15q22.31

Also known as

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

Also known asHsT17391 · ZC2HC5 · ASC-1

View full nomenclature history (5)

Alias symbolsHsT17391, ZC2HC5, ASC-1

Alias nameszinc finger, C2HC5-type, Activating Signal Cointegrator-1

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.

Pericarditis

Myocardial Ischemia

Genetic Diseases, Inborn

Proximal spinal muscular atrophy

Amyotrophic Lateral Sclerosis

Uterine Cervical 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.

Zinc fingersActivating signal cointegrator 1 complex

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.