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POC1B, POC1 centriolar protein B

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POC1B, POC1 centriolar protein B

  • POC1 proteins contain an N-terminal WD40 domain and a C-terminal coiled coil domain and are part of centrosomes. They play an important role in basal body and cilia formation. This gene encodes one of the two POC1 proteins found in humans. Mutation in this gene result in autosomal-recessive cone-rod dystrophy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]

  • Gene Synonyms (POC1 centriolar protein homolog B, WD repeat-containing protein 51B, proteome of centriole protein 1B, CORD20, PIX1, TUWD12, WDR51B,)
  • NCBI Gene ID: 282809
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0MNP0
    UNIPROT ID#>>Q8TC44
  • 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.

POC1 centriolar protein B 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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