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Publication : Lethal phenotype of mice carrying a Sept11 null mutation.

First Author  Röseler S Year  2011
Journal  Biol Chem Volume  392
Issue  8-9 Pages  779-81
PubMed ID  21824005 Mgi Jnum  J:285874
Mgi Id  MGI:6401038 Doi  10.1515/BC.2011.093
Citation  Roseler S, et al. (2011) Lethal phenotype of mice carrying a Sept11 null mutation. Biol Chem 392(8-9):779-81
abstractText  Septins are cytoskeletal GTP-binding proteins involved in processes characterized by active membrane movement, such as cytokinesis, vesicle trafficking and exocytosis. Most septins are expressed ubiquitously, however, some septins accumulate in particular tissues. The ubiquitous SEPT11 also shows high expression levels in the central nervous system and in platelets. Here, SEPT11 is involved in vesicle trafficking and may play a role in synaptic connectivity. Interestingly, mice that harbor a homozygous Sept11 null mutation, die in utero. From day 11.5 post coitum onwards, development of homozygous embryos seems to be retarded and the embryos from day 13.5 onwards were dead.
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