UBR5 (Ubiquitin Protein Ligase E3 Component N-Recognin 5) is a Protein Coding gene. Diseases associated with UBR5 include Epilepsy, Familial Adult Myoclonic, 5 and Johanson-Blizzard Syndrome. Among its related pathways are Ubiquitin mediated proteolysis and Mesodermal Commitment Pathway. Gene Ontology (GO) annotations related to this gene include RNA binding and ubiquitin-protein transferase activity. An important paralog of this gene is HERC2.