MGP Database

New search | Record Overview | Ontology/Pathway Information | Domain Information | UniProt Annotations | Related Proteins
MGP004162

Ontology/Pathway Information

Entrez Gene ID10201
Gene NameNME/NM23 nucleoside diphosphate kinase 6
Gene Symbol NME6
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005739 IDA:UniProtKBCmitochondrion
GO:0005524 IEA:UniProtKB-KWFATP binding
GO:0046872 IEA:UniProtKB-KWFmetal ion binding
GO:0004550 IDA:UniProtKBFnucleoside diphosphate kinase activity
GO:0006915 IEA:UniProtKB-KWPapoptotic process
GO:0006241 IEA:InterProPCTP biosynthetic process
GO:0006183 IEA:InterProPGTP biosynthetic process
GO:0030308 IDA:UniProtKBPnegative regulation of cell growth
GO:0045839 IDA:UniProtKBPnegative regulation of mitosis
GO:0006228 IEA:InterProPUTP biosynthetic process
SMP Pathway Links
SMP IDDescription
SMP00535Adenine phosphoribosyltransferase deficiency (APRT)
SMP00144Adenosine Deaminase Deficiency
SMP00167Adenylosuccinate Lyase Deficiency
SMP00168AICA-Ribosiduria
SMP00427Azathioprine Action Pathway
SMP00172Beta Ureidopropionase Deficiency
SMP00178Dihydropyrimidinase Deficiency
SMP00365Gout or Kelley-Seegmiller Syndrome
SMP00364Lesch-Nyhan Syndrome (LNS)
SMP00428Mercaptopurine Action Pathway
SMP00536Mitochondrial DNA depletion syndrome
SMP00202MNGIE (Mitochondrial Neurogastrointestinal Encephalopathy)
SMP00203Molybdenum Cofactor Deficiency
SMP00537Myoadenylate deaminase deficiency
SMP00050Purine Metabolism
SMP00210Purine Nucleoside Phosphorylase Deficiency
SMP00046Pyrimidine Metabolism
SMP00430Thioguanine Action Pathway
SMP00219UMP Synthase Deiciency (Orotic Aciduria)
SMP00220Xanthine Dehydrogenase Deficiency (Xanthinuria)
SMP00512Xanthinuria type I
SMP00513Xanthinuria type II
  logo