Your search for "sept9" returned 691 TaqMan® SNP Genotyping Assays
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]
AF17Q25, ESEPTIN, MSF, MSF1, NAPB, PNUTL4, SEPT9, SEPTD1, SINT1, SLPA
(Human) Q9UHD8, (Human) A8K2V3, (Human) B3KPM0, (Human) B4DTL9, (Human) B4E0N2, (Human) B4E274, (Human) B7Z654, (Human) Q96QF3, (Human) Q96QF4, (Human) Q96QF5, (Human) Q9HA04, (Human) Q9UG40, (Human) Q9Y5W4, (Mouse) Q80UG5, (Mouse) A2A6U2, (Mouse) A2A6U4, (Mouse) A2A6U6, (Mouse) Q3URP2, (Mouse) Q80TM7, (Mouse) Q9QYX9, (Rat) Q9QZR6, (Rat) Q9QZJ7, (Rat) Q9QZJ8, (Rat) Q9QZP9
Please enter the information below and press OK to send your cart to Core Services for purchase.