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SEPTIN9, septin 9

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SEPTIN9, septin 9

  • This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2009]

  • Gene Synonyms (AF17q25, MSF, MSF1, NAPB, PNUTL4, SEPT9, SINT1, SeptD1, septin-9, MLL septin-like fusion protein MSF-A, Ov/Br septin, ovarian/breast septin, septin D1,)
  • NCBI Gene ID: 10801
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A0S2Z5A5
    UNIPROT ID#>>Q9UHD8
  • 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.

septin 9 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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