PRNP (prion protein (Creutzfeld-Jakob disease, Gerstmann-Strausler-Scheinker syndrome, fatal familial insomnia)) is a gene that provides instructions to make a protein called the prion protein (PrP), which is active in the brain and several other tissues. Although the precise function of PrP is not yet known, it is possibly involved in the transport of charged atoms (ions) of copper to cells from the surrounding environment. Researchers have also proposed roles for PrP in cell signaling or in the formation of gaps between nerve cells (synapses) where cell-to-cell communication occurs.
Different forms of PrP have been identified in the nervous system. The usual cellular form is called PrPC. Another form, PrPSc, has a different 3-dimensional structure and has been associated with inherited, sporadic (non-inherited), and infectious disorders of the brain and nervous system. In a process that is not fully understood, PrPC can transform into the abnormal PrPSc. This abnormal protein can further promote the transformation of PrPC into PrPSc.
The PRNP gene is located on the short (p) arm of chromosome 20 between the end (terminus) of the arm and position 12, from base pair 4,615,068 to base pair 4,630,233.