MGP Database

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MGP000033

Ontology/Pathway Information

Entrez Gene ID54
Gene Nameacid phosphatase 5, tartrate resistant
Gene Symbol ACP5
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005829 TAS:ReactomeCcytosol
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0016021 TAS:ProtIncCintegral component of membrane
GO:0005764 IEA:UniProtKB-SubCellClysosome
GO:0003993 TAS:ReactomeFacid phosphatase activity
GO:0008199 IDA:UniProtKBFferric iron binding
GO:0008198 IDA:UniProtKBFferrous iron binding
GO:0060349 IEA:EnsemblPbone morphogenesis
GO:0045453 IEA:EnsemblPbone resorption
GO:0050830 IEA:EnsemblPdefense response to Gram-positive bacterium
GO:0050728 IEA:EnsemblPnegative regulation of inflammatory response
GO:0032695 IEA:EnsemblPnegative regulation of interleukin-12 production
GO:0032691 IEA:EnsemblPnegative regulation of interleukin-1 beta production
GO:0045019 IEA:EnsemblPnegative regulation of nitric oxide biosynthetic process
GO:0032929 IEA:EnsemblPnegative regulation of superoxide anion generation
GO:0032720 IEA:EnsemblPnegative regulation of tumor necrosis factor production
GO:0034097 IEA:EnsemblPresponse to cytokine
GO:0032496 IEA:EnsemblPresponse to lipopolysaccharide
GO:0006771 TAS:ReactomePriboflavin metabolic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0006766 TAS:ReactomePvitamin metabolic process
GO:0006767 TAS:ReactomePwater-soluble vitamin metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_169280Defective AMN causes hereditary megaloblastic anemia 1
REACT_169403Defective BTD causes biotidinase deficiency
REACT_169178Defective CD320 causes methylmalonic aciduria
REACT_169132Defective CUBN causes hereditary megaloblastic anemia 1
REACT_169415Defective GIF causes intrinsic factor deficiency
REACT_169312Defective HLCS causes multiple carboxylase deficiency
REACT_169363Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
REACT_169316Defective MMAA causes methylmalonic aciduria type cblA
REACT_169318Defective MMAB causes methylmalonic aciduria type cblB
REACT_169169Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
REACT_169256Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
REACT_169149Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
REACT_169439Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
REACT_169313Defective MUT causes methylmalonic aciduria mut type
REACT_169120Defective TCN2 causes hereditary megaloblastic anemia
REACT_169238Defects in biotin (Btn) metabolism
REACT_169429Defects in cobalamin (B12) metabolism
REACT_169385Defects in vitamin and cofactor metabolism
REACT_116125Disease
REACT_111217Metabolism
REACT_11193Metabolism of vitamins and cofactors
REACT_11238Metabolism of water-soluble vitamins and cofactors
REACT_11070Vitamin B2 (riboflavin) metabolism
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