APOL4

Gene

apolipoprotein L4

HGNCHGNC:14867 EnsemblENSG00000100336 NCBI Gene80832

Locus: gene with protein productLocation: 22q12.3

Also known as

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

Also known asAPOLIV

View full nomenclature history (1)

Alias symbolsAPOLIV

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.

Heart Septal Defects, Ventricular

COVID-19

Severe Acute Respiratory Syndrome

Central Nervous System Neoplasms

Glioma

Glioblastoma

Neoplasms

Death, Sudden, Cardiac

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.

Apolipoproteins

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.