CEP78

Gene

centrosomal protein 78

HGNCHGNC:25740 EnsemblENSG00000148019 NCBI Gene84131

Locus: gene with protein productLocation: 9q21.2

Also known as

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

Also known asC9orf81 · FLJ12643

View full nomenclature history (4)

Previous symbolsC9orf81

Alias symbolsFLJ12643

Previous nameschromosome 9 open reading frame 81, centrosomal protein 78kDa

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.

Cone rod dystrophy

Cone-rod dystrophy

Central Nervous System Neoplasms

Genetic Diseases, Inborn

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.

Centriolar satellite proteins

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.