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Septin-5

Known as: PNUTL1, SEPT5, Cell Division Control-Related Protein 1 
Septin-5 (369 aa, ~43 kDa) is encoded by the human SEPT5 gene. This protein plays a role in cytokinesis.
National Institutes of Health

Related topics

Related topics

11 relations
Cell Cycle ControlCytokinesisCytoskeletonGenes, Regulator

Papers overview

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2018
2018
Deletion of human GP 1 BB and SEPT 5 is associated with Bernard-Soulier syndrome , platelet secretion defect , polymicrogyria , and develop-mental delay
Ingrid Bartsch1; Kirstin Sandrock1; Francois Lanza2; Paquita Nurden3; Ina Hainmann1; Anna Pavlova4; Andreas Greinacher5; Uta… 
2018
2018
Autoimmune Septin-5 Cerebellar Ataxia
  • L. Wilkins
  • Neurology: Neuroimmunology & Neuroinflammation
  • 2018
  • Corpus ID: 56894627
[This corrects the article on p. e474 in vol. 5, PMID: 29998156.]. 
2017
2017
NEURODEGENERATIVE DSORDERS USING ATFPS-PEPTIDE
  • 2017
  • Corpus ID: 55542302
Amin et al., “Cyclin-Dependent Kinase 5 Phosphorylation of Human Septin SEPT5 (hCDCrel-1) Modulates Exocytosis.” The Journal of… 
2010
2010
Avaliação da expressão do gene SEPT5 em pacientes portadores de leucemia mielóide crônica
A leucemia mieloide cronica (LMC) e uma doenca mieloproliferativa, que pode ser dividida em tres fases clinicas, sendo a fase… 
2004
2004
Genetic deletion of mouse platelet glycoprotein Ibproduces
Here we report the characterization of a mouse model of the Bernard-Soulier syndrome generated by a targeted disruption of the… 
2001
2001
Meiosis: Synapsis spoilt
Does parkin have other substrates, and is one of CDCrel1’s normal functions to block dopamine release? If it is, blockage of… 
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