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CEP152

Gene

centrosomal protein 152

HGNCHGNC:29298EnsemblENSG00000103995NCBI Gene22995
Locus: gene with protein productLocation: 15q21.1

Also known as

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

Also known asKIAA0912 · SCKL5 · MCPH9
View full nomenclature history (5)
Alias symbolsKIAA0912, SCKL5, MCPH9
Previous namescentrosomal protein 152kDa
Alias namesasterless

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
Seckel syndrome
Neurodegenerative Diseases
Microcephalic primordial dwarfism
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.

Provenance

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