Back to discover

CEP128

Gene

centrosomal protein 128

HGNCHGNC:20359EnsemblENSG00000100629NCBI Gene145508
Locus: gene with protein productLocation: 14q31.1

Also known as

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

Also known asC14orf61 · C14orf145
View full nomenclature history (5)
Previous symbolsC14orf61, C14orf145
Previous nameschromosome 14 open reading frame 61, chromosome 14 open reading frame 145, centrosomal protein 128kDa

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.

Hypothyroidism
hypothyroidism due to TSH receptor mutations
familial hyperthyroidism due to mutations in TSH receptor
Graves' Disease
Hyperthyroidism
Epilepsy
Myxedema
Joint Diseases
Ovarian neoplasm

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.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.