PTPRN2 (protein tyrosine phosphatase, receptor type, N polypeptide 2) is a protein-coding gene. Diseases associated with PTPRN2 include melkersson-rosenthal syndrome, and multiple cranial nerve palsy, and among its related super-pathways are Allograft rejection and PAK Pathway. GO annotations related to this gene include transmembrane receptor protein tyrosine phosphatase activity. An important paralog of this gene is PTPRN.
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Type I diabetes mellitus.
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