XB-FEAT-1012201: Difference between revisions
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This is the community wiki page for the gene '' | This is the community wiki page for the gene ''sepint9'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes= | =nomenclature changes= | ||
Revision as of 09:47, 15 May 2019
septin9
This is the community wiki page for the gene sepint9 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
05.13.19 Human symbol has changed for Entrez Gene: 10801. From SEPT9 to SEPTIN9
Summary from NCBI for human SEPTIN9
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]