MGP Database

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MGP005501

Ontology/Pathway Information

Entrez Gene ID55811
Gene Nameadenylate cyclase 10 (soluble)
Gene Symbol ADCY10
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0045177 IEA:EnsemblCapical part of cell
GO:0030424 IEA:EnsemblCaxon
GO:0045178 IEA:EnsemblCbasal part of cell
GO:0005737 TAS:ProtIncCcytoplasm
GO:0005856 IEA:UniProtKB-SubCellCcytoskeleton
GO:0005829 NAS:UniProtKBCcytosol
GO:0030425 IEA:EnsemblCdendrite
GO:0030426 IEA:EnsemblCgrowth cone
GO:0043025 IEA:EnsemblCneuronal cell body
GO:0048471 IEA:UniProtKB-SubCellCperinuclear region of cytoplasm
GO:0005886 IEA:UniProtKB-SubCellCplasma membrane
GO:0004016 NAS:UniProtKBFadenylate cyclase activity
GO:0005524 IEA:UniProtKB-KWFATP binding
GO:0000287 IEA:InterProFmagnesium ion binding
GO:0030145 IEA:EnsemblFmanganese ion binding
GO:0006171 NAS:UniProtKBPcAMP biosynthetic process
GO:0035556 IEA:InterProPintracellular signal transduction
GO:0043065 IEA:EnsemblPpositive regulation of apoptotic process
GO:0007283 IEA:InterProPspermatogenesis
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_268323Hedgehog 'off' state
REACT_264508Signaling by Hedgehog
REACT_111102Signal Transduction
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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