SEPT9 Polyclonal Antibody, 100ul Oligo Pool Mutations in this gene have

Mutations in this gene have been associated with congenital myasthenic syndrome

remodelling of membrane lipids

The gene product is predicted to be a six-transmembrane protein

but is limited in neural organs in normal tissues

SEPT9 Polyclonal Antibody, 100ul Oligo Pool Mutations in this gene haveThis 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