MGP Database

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MGP003618

Ontology/Pathway Information

Entrez Gene ID8611
Gene Namephosphatidic acid phosphatase type 2A
Gene Symbol PPAP2A
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0005887 NAS:UniProtKBCintegral component of plasma membrane
GO:0016020 IDA:UniProtKBCmembrane
GO:0005886 TAS:ReactomeCplasma membrane
GO:0008195 IDA:UniProtKBFphosphatidate phosphatase activity
GO:0030521 NAS:UniProtKBPandrogen receptor signaling pathway
GO:0008354 TAS:ProtIncPgerm cell migration
GO:0030518 TAS:UniProtKBPintracellular steroid hormone receptor signaling pathway
GO:0006629 NAS:ProtIncPlipid metabolic process
GO:0008285 NAS:UniProtKBPnegative regulation of cell proliferation
GO:0046839 TAS:UniProtKBPphospholipid dephosphorylation
GO:0006470 IEA:EnsemblPprotein dephosphorylation
GO:0007205 TAS:UniProtKBPprotein kinase C-activating G-protein coupled receptor signaling pathway
GO:0019216 NAS:UniProtKBPregulation of lipid metabolic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0030148 TAS:ReactomePsphingolipid biosynthetic process
GO:0006665 TAS:ReactomePsphingolipid metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_111217Metabolism
REACT_22258Metabolism of lipids and lipoproteins
REACT_115810Sphingolipid de novo biosynthesis
REACT_19323Sphingolipid metabolism
SMP Pathway Links
SMP IDDescription
SMP00529D-glyceric acidura
SMP00525Fabry disease
SMP00530Familial lipoprotein lipase deficiency
SMP00349Gaucher Disease
SMP00348Globoid Cell Leukodystrophy
SMP00039Glycerolipid Metabolism
SMP00187Glycerol Kinase Deficiency
SMP00526Krabbe disease
SMP00347Metachromatic Leukodystrophy (MLD)
SMP00025Phospholipid Biosynthesis
SMP00479Plasmalogen Synthesis
SMP00034Sphingolipid Metabolism
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