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CEP152, centrosomal protein 152

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CEP152, centrosomal protein 152

  • This gene encodes a protein that is thought to be involved with centrosome function. Mutations in this gene have been associated with primary microcephaly (MCPH4). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]

  • Gene Synonyms (MCPH4, MCPH9, SCKL5, centrosomal protein of 152 kDa, asterless, centrosomal protein 152kDa, microcephaly, primary autosomal recessive 4,)
  • NCBI Gene ID: 22995
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q3B7A2
    UNIPROT ID#>>O94986
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

centrosomal protein 152 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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