靶标：
SEPTIN9
产品别名：
AF17q25； MSF； MSF1； NAPB； PNUTL4； SEPT9； SINT1； SeptD1； SEPTIN9； septin 9； septin 9； septin-9； MLL septin-like fusion protein MSF-A； Ov/Br septin； ovarian/breast septin； septin D1； 细胞周期调控蛋白D1；
背景信息：
septin 9(SEPT9) Homo sapiens 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],
