POC1A

Gene

POC1 centriolar protein A

HGNCHGNC:24488 EnsemblENSG00000164087 NCBI Gene25886

Locus: gene with protein productLocation: 3p21.2

Also known as

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

Also known asWDR51A · DKFZP434C245

View full nomenclature history (4)

Previous symbolsWDR51A

Alias symbolsDKFZP434C245

Previous namesWD repeat domain 51A, POC1 centriolar protein homolog A (Chlamydomonas)

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 primary microcephaly

Non-acquired isolated growth hormone deficiency

Genetic Diseases, Inborn

Microcephaly

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.

WD repeat domain containing

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.