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Gene entry

CEP152

centrosomal protein 152

Chromosome
15
Cytoband
15q21.1
Variants (rsID)
46

CEP152 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q21.1). Its official name is “centrosomal protein 152”. The reference table lists 46 variants (rsID) for this gene.

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Clinically classified variants

17 reference-table entries with clinical significance.

  • rs150910683Benignsingle nucleotide variantSeckel syndrome 5|Microcephaly 9, primary, autosomal recessive
  • rs200879436Benignsingle nucleotide variantSeckel syndrome 5
  • rs368764302Benignsingle nucleotide variantMicrocephaly 9, primary, autosomal recessive|Seckel syndrome 5
  • rs74012142Benignsingle nucleotide variantMicrocephaly 9, primary, autosomal recessive|Seckel syndrome 5
  • rs80090788Benignsingle nucleotide variantMicrocephaly 9, primary, autosomal recessive|Seckel syndrome 5
  • rs145138194Conflicting interpretationssingle nucleotide variantMicrocephaly 9, primary, autosomal recessive|Seckel syndrome 5
  • rs181295720Conflicting interpretationssingle nucleotide variantMicrocephaly 9, primary, autosomal recessive|Seckel syndrome 5
  • rs182018947Conflicting interpretationssingle nucleotide variantMicrocephaly 9, primary, autosomal recessive|CEP152-Related Disorders|Seckel syndrome 5|Seckel syndrome 5|Microcephaly 9, primary, autosomal recessive
  • rs188101277Conflicting interpretationssingle nucleotide variantMicrocephaly 9, primary, autosomal recessive|Seckel syndrome 5
  • rs199862615Conflicting interpretationssingle nucleotide variantMicrocephaly 9, primary, autosomal recessive|Seckel syndrome 5
  • rs201217824Conflicting interpretationssingle nucleotide variantMicrocephaly 9, primary, autosomal recessive|Seckel syndrome 5
  • rs74553953Conflicting interpretationssingle nucleotide variantSeckel syndrome 5|Microcephaly 9, primary, autosomal recessive
  • rs77745570Conflicting interpretationssingle nucleotide variantMicrocephaly 9, primary, autosomal recessive|Seckel syndrome 5
  • rs199777941Likely benignsingle nucleotide variant
  • rs267606717Pathogenicsingle nucleotide variantMicrocephaly 9, primary, autosomal recessive|Seckel syndrome 5|Microcephaly 9, primary, autosomal recessive|CEP152-Related Disorders
  • rs137967275Uncertain significancesingle nucleotide variantCEP152-Related Disorders
  • rs147595936Uncertain significancesingle nucleotide variant

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.