| Entrez gene ID | | 10801 |
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| Official gene symbol | | SEPT9 |
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| Full name | | septin 9 |
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| Aliases | | ,AF17q25,FLJ75490,KIAA0991,MSF,MSF1,NAPB,PNUTL4,SINT1,SeptD1, |
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| Gene summary | | 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. |
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| Location | | Chromosome: 17 Locus: 17q25 |
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| Gene position | | 75277492 - 75496678 Map Viewer |
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| Gene orientation | | plus |
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| Gene size | | 219187 bp |
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| Gene sequence |
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| OMIM ID | | 604061 |
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