TRIP13

Gene

thyroid hormone receptor interactor 13

HGNCHGNC:12307 EnsemblENSG00000071539 NCBI Gene9319

Locus: gene with protein productLocation: 5p15.33

Also known as

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

Also known as16E1BP

View full nomenclature history (2)

Alias symbols16E1BP

Alias namesthyroid receptor interacting protein 13

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.

Neurodegenerative Diseases

Wilms Tumor

Lysosomal Storage Diseases

Carcinoma, Hepatocellular

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.

AAA ATPases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-01-29.

Open TargetsGene–disease associations from the Open Targets Platform.