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Protein-coding gene in the species Homo sapiens
Periaxin is a protein that in humans is encoded by the PRX gene .[ 5] [ 6] [ 7]
The PRX gene encodes L- and S-periaxin, proteins of myelinating Schwann cells , and is mutated in Dejerine–Sottas syndrome (MIM 145900) and Charcot–Marie–Tooth disease type 4F (MIM 145900).[supplied by OMIM][ 7]
^ a b c GRCh38: Ensembl release 89: ENSG00000105227 – Ensembl , May 2017^ a b c GRCm38: Ensembl release 89: ENSMUSG00000053198 – Ensembl , May 2017^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .^ Gillespie CS, Sherman DL, Fleetwood-Walker SM, Cottrell DF, Tait S, Garry EM, Wallace VC, Ure J, Griffiths IR, Smith A, Brophy PJ (Jun 2000). "Peripheral demyelination and neuropathic pain behavior in periaxin-deficient mice" . Neuron . 26 (2): 523– 31. doi :10.1016/S0896-6273(00)81184-8 PMID 10839370 . ^ Gillespie CS, Lee M, Fantes JF, Brophy PJ (Jul 1997). "The gene encoding the Schwann cell protein periaxin localizes on mouse chromosome 7 (Prx)". Genomics . 41 (2): 297– 8. doi :10.1006/geno.1997.4630 . PMID 9143514 . ^ a b "Entrez Gene: PRX periaxin" .
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