ZC3H14

Gene

zinc finger CCCH-type containing 14

HGNCHGNC:20509 EnsemblENSG00000100722 NCBI Gene79882

Locus: gene with protein productLocation: 14q31.3

Also known as

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

Also known asFLJ11806 · UKp68 · NY-REN-37

View full nomenclature history (3)

Alias symbolsFLJ11806, UKp68, NY-REN-37

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.

Autosomal recessive non-syndromic intellectual disability

Alzheimer's Disease

Amyotrophic Lateral Sclerosis

Tauopathies

Fuchs' Endothelial Dystrophy

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 CCCH-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.