Gene: SEPTIN9

Alternate names for this Gene: AF17q25|MSF|MSF1|NAPB|PNUTL4|SEPT9|SINT1|SeptD1

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.

Gene is located in Chromosome: 17

Location in Chromosome : 17q25.3

Description of this Gene: septin 9

Type of Gene: protein-coding

Gene: LOC112268199

Alternate names for this Gene:

Gene Summary:

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rs312907 in SEPTIN9;LOC112268199 gene and Leukemia, Myelocytic, Acute PMID 27903959 2017 Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.