MGP Database

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MGP000825

Ontology/Pathway Information

Entrez Gene ID1716
Gene Namedeoxyguanosine kinase
Gene Symbol DGUOK
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005829 IEA:EnsemblCcytosol
GO:0005759 TAS:ReactomeCmitochondrial matrix
GO:0005739 TAS:ProtIncCmitochondrion
GO:0005634 IDA:UniProtKBCnucleus
GO:0005524 IEA:UniProtKB-KWFATP binding
GO:0004138 IDA:UniProtKBFdeoxyguanosine kinase activity
GO:0019206 EXP:ReactomeFnucleoside kinase activity
GO:0009157 IDA:GOCPdeoxyribonucleoside monophosphate biosynthetic process
GO:0046070 IEA:EnsemblPdGTP metabolic process
GO:0008617 TAS:ProtIncPguanosine metabolic process
GO:0010977 IEA:EnsemblPnegative regulation of neuron projection development
GO:0055086 TAS:ReactomePnucleobase-containing small molecule metabolic process
GO:0009165 EXP:GOCPnucleotide biosynthetic process
GO:0006468 IEA:EnsemblPprotein phosphorylation
GO:0043101 TAS:ReactomePpurine-containing compound salvage
GO:0046122 IDA:UniProtKBPpurine deoxyribonucleoside metabolic process
GO:0006144 TAS:ReactomePpurine nucleobase metabolic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_111217Metabolism
REACT_1698Metabolism of nucleotides
REACT_522Purine metabolism
REACT_1923Purine salvage
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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