FOXJ2

Gene

forkhead box J2

HGNCHGNC:24818 EnsemblENSG00000065970 NCBI Gene55810

Locus: gene with protein productLocation: 12p13.31

Also known as

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

Also known asFHX

View full nomenclature history (1)

Alias symbolsFHX

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.

Carcinoma, Hepatocellular

Neoplasms

Nasopharyngeal Carcinoma

Colorectal Neoplasms

Androgen insensitivity syndrome

Ovarian carcinoma

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.

Forkhead boxes

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.