CYP4F2

Gene

cytochrome P450 family 4 subfamily F member 2

HGNCHGNC:2645 EnsemblENSG00000186115 NCBI Gene8529

Locus: gene with protein productLocation: 19p13.12

Also known as

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

View full nomenclature history (2)

Previous namescytochrome P450, subfamily IVF, polypeptide 2, cytochrome P450, family 4, subfamily F, polypeptide 2

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.

Diabetic Neuropathies

Peripheral Nervous System Diseases

Coronary Artery Disease

Retinitis Pigmentosa

Early-onset non-syndromic cataract

Posterior polar cataract

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.

Cytochrome P450 family 4

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-06-10.

Open TargetsGene–disease associations from the Open Targets Platform.