Last revised by Daniel J Bell on 28 Dec 2018

Neurofibromin is a protein coded for by the NF1 gene located on chromosome 17 (17q11.2). It is a multifunctional protein and is involved in the regulation of many cellular signaling pathways. In patients with a mutation of the NF1 gene, neurofibromin is defective and results in the clinical syndromes of NF1 and NF2.

The protein is expressed in all cell types and is predominantly a cytoplasmic protein. However, in some cell types, neurofibromin has been found within the nucleus 1. It predominates in neurons, Schwann cells, oligodendrocytes, astrocytes and leukocytes 2.

It has a number of regulatory behaviors 1:

  • RAS/MAPK pathway
  • mTOR pathway
  • adenylate cyclase activity
  • interacts with a number of other proteins, e.g. microtubulin, kinesin-1, protein kinase A and C, caveolin and amyloid precursor protein

Its regulatory behavior impacts cell growth and proliferation. It mainly acts by regulating the activity of the RAS-family proteins. The neurofibromin protein belongs to a group of proteins called the Ras GTPase-activating proteins (GAP). Their activity is mediated by accelerating the hydrolysis of GTP bound to active RAS protein.

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