ANK2

Gene

ankyrin 2

HGNCHGNC:493 EnsemblENSG00000145362 NCBI Gene287

Locus: gene with protein productLocation: 4q25-q26

Also known as

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

Also known asLQT4 · FAP87 · CFAP87

View full nomenclature history (5)

Previous symbolsLQT4

Alias symbolsFAP87, CFAP87

Previous nameslong (electrocardiographic) QT syndrome 4, ankyrin 2, neuronal

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.

Neurodevelopmental Disorders

Complex neurodevelopmental disorder

Genetic Diseases, Inborn

Epilepsy

Autism Spectrum Disorder

Brugada syndrome

Myocardial Ischemia

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.

Ankyrin repeat domain containingCilia and flagella associatedMicroRNA protein coding host genesZU5 domain containing

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.