PLPP4
Phospholipid phosphatase 4
Also known as: DPPL2, PLPP4_HUMAN, PPAPDC1, PPAPDC1A
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5VZY2
- Gene
- PLPP4
- Ensembl
- ENSG00000203805
- Chromosome
- 10
- Canonical length
- 271 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Nucleoli rim
OverviewNCBI Gene
Enables diacylglycerol diphosphate phosphatase activity; identical protein binding activity; and phosphatidate phosphatase activity. Involved in phospholipid dephosphorylation and regulation of calcium ion import. Predicted to be located in plasma membrane. Predicted to be active in membrane. Biomarker of breast cancer. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
271 residues, UniProt reviewed canonical sequence.
>Q5VZY2|PLPP4
1 MRELAIEIGV RALLFGVFVF TEFLDPFQRV IQPEEIWLYK NPLVQSDNIP TRLMFAISFL
61 TPLAVICVVK IIRRTDKTEI KEAFLAVSLA LALNGVCTNT IKLIVGRPRP DFFYRCFPDG
121 VMNSEMHCTG DPDLVSEGRK SFPSIHSSFA FSGLGFTTFY LAGKLHCFTE SGRGKSWRLC
181 AAILPLYCAM MIALSRMCDY KHHWQDSFVG GVIGLIFAYI CYRQHYPPLA NTACHKPYVS
241 LRVPASLKKE ERPTADSAPS LPLEGITEGP VLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLPP4 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 6
- Mean surface accessibility (rSASA)
- 0.31
- Highest tissue expression
- 2 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 2 nTPM
- hypothalamus: 1.7 nTPM
- hippocampal formation: 1.6 nTPM
- midbrain: 1.5 nTPM
- amygdala: 1.2 nTPM
- cerebral cortex: 1.2 nTPM
Single-cell type
- oligodendrocyte progenitor cells: 322 nCPM
- renal connecting tubule cells: 157 nCPM
- renal collecting duct intercalated cells: 119 nCPM
- leydig cells: 66 nCPM
- erythrocyte progenitors: 63 nCPM
- brain excitatory neurons: 60 nCPM
Immune cell
- basophil: 0.6 nTPM
- neutrophil: 0.2 nTPM
- NK-cell: 0.1 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- pons: 27 nTPM
- hypothalamus: 21 nTPM
- medulla oblongata: 17 nTPM
- cerebellum: 15 nTPM
- midbrain: 13 nTPM
- hippocampal formation: 13 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.02
- gnomAD pLI
- 0
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- blastocyst hatching
- Fc-gamma receptor signaling pathway involved in phagocytosis
- phospholipid dephosphorylation
- phospholipid metabolic process
- regulation of calcium ion import
Molecular functions
- diacylglycerol diphosphate phosphatase activity
- identical protein binding
- phosphatidate phosphatase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PLPP4 as an antibody target. Whether an autoantibody or antibody against PLPP4 could matter depends on whether native PLPP4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLPP4 is annotated at the cell surface, where native PLPP4 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label PLPP4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...