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Gene entry

CDK5RAP2

CDK5 regulatory subunit associated protein 2

Chromosome
9
Cytoband
9q33.2
Variants (rsID)
43

CDK5RAP2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q33.2). Its official name is “CDK5 regulatory subunit associated protein 2”. The reference table lists 43 variants (rsID) for this gene.

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Clinically classified variants

16 reference-table entries with clinical significance.

  • rs139706626Benignsingle nucleotide variantMicrocephaly 3, primary, autosomal recessive
  • rs34523498Benignsingle nucleotide variantMicrocephaly 3, primary, autosomal recessive
  • rs35909061Benignsingle nucleotide variantMicrocephaly 3, primary, autosomal recessive
  • rs41296081Benignsingle nucleotide variantMicrocephaly 3, primary, autosomal recessive
  • rs114128928Conflicting interpretationssingle nucleotide variantPrimary Microcephaly, Recessive
  • rs146839668Conflicting interpretationssingle nucleotide variantMicrocephaly 3, primary, autosomal recessive
  • rs587783393Conflicting interpretationsDeletionMicrocephaly 3, primary, autosomal recessive
  • rs587783396Conflicting interpretationssingle nucleotide variantMicrocephaly 3, primary, autosomal recessive
  • rs61758368Conflicting interpretationssingle nucleotide variantMicrocephaly 3, primary, autosomal recessive
  • rs7030969Conflicting interpretationssingle nucleotide variantPrimary Microcephaly, Recessive
  • rs76132121Conflicting interpretationssingle nucleotide variantPrimary Microcephaly, Recessive
  • rs13287734Uncertain significancesingle nucleotide variantMicrocephaly 3, primary, autosomal recessive
  • rs138526640Uncertain significancesingle nucleotide variantMicrocephaly 3, primary, autosomal recessive
  • rs185208659Uncertain significancesingle nucleotide variantMicrocephaly 3, primary, autosomal recessive
  • rs35199933Uncertain significancesingle nucleotide variantMicrocephaly 3, primary, autosomal recessive
  • rs41309342Not classifiedsingle nucleotide variantMicrocephaly 3, primary, autosomal recessive

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.