NME5 (NME/NM23 Family Member 5) is a Protein Coding gene.
Diseases associated with NME5 include Muscular Dystrophy, Rigid Spine, 1.
Among its related pathways are superpathway of pyrimidine deoxyribonucleotides de novo biosynthesis and purine nucleotides de novo biosynthesis.
GO annotations related to this gene include nucleoside diphosphate kinase activity.
An important paralog of this gene is NME7.