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MKS1, MKS transition zone complex subunit 1

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MKS1, MKS transition zone complex subunit 1

  • The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

  • Gene Synonyms (Meckel syndrome type 1 protein, POC12 centriolar protein homolog, BBS13, JBTS28, MES, MKS, POC12,)
  • NCBI Gene ID: 54903
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A0S2Z5Z2
    UNIPROT ID#>>H0Y2S2
    UNIPROT ID#>>B4DVC5
    UNIPROT ID#>>Q9NXB0
  • 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.

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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