ZCCHC2

Gene

zinc finger CCHC-type containing 2

HGNCHGNC:22916 EnsemblENSG00000141664 NCBI Gene54877

Locus: gene with protein productLocation: 18q21.33

Also known as

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

Also known asC18orf49 · FLJ20281 · KIAA1744 · FLJ20222

View full nomenclature history (5)

Previous symbolsC18orf49

Alias symbolsFLJ20281, KIAA1744, FLJ20222

Previous nameschromosome 18 open reading frame 49

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.

Coronary Artery Disease

bone Paget'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.

Zinc fingers CCHC-type

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.