ING1

Gene

inhibitor of growth family member 1

HGNCHGNC:6062 EnsemblENSG00000153487 NCBI Gene3621

Locus: gene with protein productLocation: 13q34

Also known as

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

Also known asp33ING1 · p33ING1b · p24ING1c · p33 · p47 · p47ING1a

View full nomenclature history (10)

Alias symbolsp33ING1, p33ING1b, p24ING1c, p33, p47, p47ING1a

Alias namesgrowth inhibitor ING1, inhibitor of growth 1, tumor suppressor ING1, growth inhibitory protein ING1

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.

Squamous Cell Carcinoma of Head and Neck

Atrial Fibrillation

Neurodegenerative Diseases

Coronary Artery Disease

Colorectal adenocarcinoma

Temporomandibular Joint Disorders

Heart Failure

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.

PHD finger proteins

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.