PNPLA4
Patatin-like phospholipase domain-containing protein 4
Also known as: DXS1283E, GS2, iPLA2eta, PLPL4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P41247
- Gene
- PNPLA4
- Ensembl
- ENSG00000006757
- Chromosome
- X
- Canonical length
- 253 aa
- Protein class
- Disease related genes, Enzymes, Metabolic proteins, Plasma proteins, Potential drug targets, Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a member of the patatin-like family of phospholipases. The encoded enzyme has both triacylglycerol lipase and transacylase activities and may be involved in adipocyte triglyceride homeostasis. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome Y. [provided by RefSeq, Feb 2010]
Canonical amino-acid sequenceUniProt
253 residues, UniProt reviewed canonical sequence.
>P41247|PNPLA4
1 MKHINLSFAA CGFLGIYHLG AASALCRHGK KLVKDVKAFA GASAGSLVAS VLLTAPEKIE
61 ECNQFTYKFA EEIRRQSFGA VTPGYDFMAR LRSGMESILP PSAHELAQNR LHVSITNAKT
121 RENHLVSTFS SREDLIKVLL ASSFVPIYAG LKLVEYKGQK WVDGGLTNAL PILPVGRTVT
181 ISPFSGRLDI SPQDKGQLDL YVNIAKQDIM LSLANLVRLN QALFPPSKRK MESLYQCGFD
241 DTVKFLLKEN WFELocalizationUniProt · AlphaFold · HPA
Whether an antibody against PNPLA4 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.24
- Highest tissue expression
- 73 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 73 nTPM
- tongue: 62 nTPM
- heart muscle: 40 nTPM
- kidney: 38 nTPM
- liver: 37 nTPM
- choroid plexus: 29 nTPM
Single-cell type
- esophageal suprabasal cells: 131 nCPM
- parietal cells: 106 nCPM
- oocytes: 101 nCPM
- esophageal apical cells: 86 nCPM
- hepatocytes: 79 nCPM
- esophageal basal cells: 76 nCPM
Immune cell
- myeloid DC: 22 nTPM
- naive B-cell: 17 nTPM
- plasmacytoid DC: 16 nTPM
- memory B-cell: 15 nTPM
- intermediate monocyte: 14 nTPM
- non-classical monocyte: 13 nTPM
Brain region
- choroid plexus: 29 nTPM
- hypothalamus: 26 nTPM
- thalamus: 24 nTPM
- midbrain: 22 nTPM
- basal ganglia: 20 nTPM
- medulla oblongata: 20 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)
- 1.27
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.15
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- acylglycerol O-acyltransferase activity
- all-trans-retinyl-palmitate hydrolase, all-trans-retinol forming activity
- diolein transacylation activity
- mono-olein transacylation activity
- phospholipase A2 activity
- retinyl-palmitate esterase activity
- triacylglycerol lipase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Patatin-like phospholipase domain
- Acyl transferase/acyl hydrolase/lysophospholipase
- Patatin-like phospholipase domain-containing protein
- Patatin-like phospholipase
- Patatin-like phospholipase domain-containing protein 4
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PNPLA4 as an antibody target. Whether an autoantibody or antibody against PNPLA4 could matter depends on whether native PNPLA4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PNPLA4 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label PNPLA4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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