ZCCHC18

Gene

zinc finger CCHC-type containing 18

HGNCHGNC:32459 EnsemblENSG00000166707 NCBI Gene644353

Locus: gene with protein productLocation: Xq22.2

Also known as

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

Also known asSIZN2 · PNMA7B

View full nomenclature history (4)

Alias symbolsSIZN2, PNMA7B

Previous nameszinc finger, CCHC domain containing 12 pseudogene 1

Alias namesparaneoplastic Ma antigen family member 7B

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.

Leukemia, Lymphocytic, Chronic, B-Cell

Osteoarthritis, Hip

Ataxia Telangiectasia

Leukemia, Myeloid, Acute

Precursor Cell Lymphoblastic Leukemia-Lymphoma

Pituitary Neoplasms

Lymphoma, Large B-Cell, Diffuse

Thyroid gland carcinoma

Thyroid Neoplasms

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-typeParaneoplastic Ma antigens

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.