WDR62

Gene

WD repeat domain 62

HGNCHGNC:24502 EnsemblENSG00000075702 NCBI Gene284403

Locus: gene with protein productLocation: 19q13.12

Also known as

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

Also known asC19orf14 · MCPH2 · DKFZP434J046 · FLJ33298

View full nomenclature history (6)

Previous symbolsC19orf14, MCPH2

Alias symbolsDKFZP434J046, FLJ33298

Previous namesmicrocephaly, primary autosomal recessive 2, chromosome 19 open reading frame 14

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

Genetic Diseases, Inborn

Atrial Fibrillation

Glomerulonephritis, Membranous

Microcephaly 1, primary, autosomal recessive

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.