ACAP3

Gene

ArfGAP with coiled-coil, ankyrin repeat and PH domains 3

HGNCHGNC:16754 EnsemblENSG00000131584 NCBI Gene116983

Locus: gene with protein productLocation: 1p36.33

Also known as

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

Also known asCENTB5 · KIAA1716

View full nomenclature history (3)

Previous symbolsCENTB5

Alias symbolsKIAA1716

Previous namescentaurin, beta 5

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

Hair color

Epilepsy

Inflammatory Bowel Diseases

Osteoarthritis

Zika Virus Infection

Differentiated thyroid carcinoma

Thyroid gland papillary carcinoma

Parkinson's Disease

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.

ArfGAPsAnkyrin repeat domain containingBAR-PH domain containingMicroRNA protein coding host genes

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.