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FOXN3

Gene

forkhead box N3

HGNCHGNC:1928EnsemblENSG00000053254NCBI Gene1112
Locus: gene with protein productLocation: 14q31.3-q32.11

Also known as

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

Also known asC14orf116 · CHES1
View full nomenclature history (4)
Previous symbolsC14orf116, CHES1
Previous namescheckpoint suppressor 1, chromosome 14 open reading frame 116

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
Intelligence
Diabetes Mellitus, Type 2
Brain Neoplasms
Alcohol drinking
Diabetes Mellitus
Heart Failure
Risk-taking behaviour
Heart Diseases

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.