MGP Database

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MGP004468

Ontology/Pathway Information

Entrez Gene ID11164
Gene Namenudix (nucleoside diphosphate linked moiety X)-type motif 5
Gene Symbol NUDT5
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005829 TAS:ReactomeCcytosol
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0005622 NAS:UniProtKBCintracellular
GO:0005634 IDA:UniProtKBCnucleus
GO:0047631 EXP:ReactomeFADP-ribose diphosphatase activity
GO:0019144 IDA:UniProtKBFADP-sugar diphosphatase activity
GO:0000287 IDA:UniProtKBFmagnesium ion binding
GO:0017110 IEA:EnsemblFnucleoside-diphosphatase activity
GO:0030515 ISS:UniProtKBFsnoRNA binding
GO:0019303 NAS:UniProtKBPD-ribose catabolic process
GO:0034656 TAS:ReactomePnucleobase-containing small molecule catabolic process
GO:0055086 TAS:ReactomePnucleobase-containing small molecule metabolic process
GO:0009117 NAS:ProtIncPnucleotide metabolic process
GO:0009191 IDA:UniProtKBPribonucleoside diphosphate catabolic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_111217Metabolism
REACT_1698Metabolism of nucleotides
REACT_150237Phosphate bond hydrolysis by NUDT proteins
SMP Pathway Links
SMP IDDescription
SMP00535Adenine phosphoribosyltransferase deficiency (APRT)
SMP00144Adenosine Deaminase Deficiency
SMP00167Adenylosuccinate Lyase Deficiency
SMP00168AICA-Ribosiduria
SMP00427Azathioprine Action Pathway
SMP00365Gout or Kelley-Seegmiller Syndrome
SMP00364Lesch-Nyhan Syndrome (LNS)
SMP00428Mercaptopurine Action Pathway
SMP00536Mitochondrial DNA depletion syndrome
SMP00203Molybdenum Cofactor Deficiency
SMP00537Myoadenylate deaminase deficiency
SMP00050Purine Metabolism
SMP00210Purine Nucleoside Phosphorylase Deficiency
SMP00430Thioguanine Action Pathway
SMP00220Xanthine Dehydrogenase Deficiency (Xanthinuria)
SMP00512Xanthinuria type I
SMP00513Xanthinuria type II
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