Gene
CEP152
centrosomal protein 152
- HGNC 29298(opens in a new tab)
- Ensembl gene ENSG00000103995(opens in a new tab)
- NCBI Gene 22995(opens in a new tab)
Summary
- Cytogenetic location
- 15q21.1
- Coordinates
- Chromosome 15: 48,737,938–48,811,069 (GRCh38)
- Exons
- 27 exons across 73.1 kb
- Protein
- 1,710 amino acids
- Also known as
- KIAA0912, SCKL5, MCPH9
- MANE Select transcript
- ENST00000380950.7NM_001194998.2
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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No Genome Test report reads CEP152 yet. The test sequences your whole genome, so your data includes it all the same.
How CEP152 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 5.6 kb of the gene's 73.1 kb; 5,133 of those bases code for the protein.
How a genome test reads CEP152
35
positions in CEP152 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 73.1 kb of CEP152, introns included, not only the 5.6 kb of exons.
Traits linked to CEP152
The Human Phenotype Ontology lists these as features of the rare conditions CEP152 can cause. Each trait's page lists the other genes linked to it.
Abnormality of head or neck
- Abnormally small head
- Beaked nose
- Little lower jaw
- Sloping forehead
- Absence of a tooth
- Deformity of the skull
- High palate
- Narrow face
Show 14 more traits
- Thin red part of the upper lip
- Upward slanting of the opening between the eyelids
- Abnormal tooth enamel
- Decreased number of teeth
- Downward slanting of the opening between the eyelids
- Narrow opening between the eyelids
- Sparse scalp hair
- Thin dental enamel
- Cleft palate
- Facial asymmetry
- Failure of development of between one and six teeth
- Failure of development of more than six teeth
- Prominent nasal bridge
- Receding chin
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). CEP152 gene: centrosomal protein 152. Retrieved 17 October 2026, from https://dantelabs.com/genes/cep152
Dante Labs. CEP152 gene: centrosomal protein 152 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/cep152
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