PNLIPRP2
Pancreatic lipase-related protein 2
Also known as: LIPR2_HUMAN
Protein identityUniProt · HPA
- UniProt accession
- P54317
- Gene
- PNLIPRP2
- Canonical length
- 469 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
OverviewNCBI Gene
No narrative summary is available for PNLIPRP2 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
469 residues, UniProt reviewed canonical sequence.
>P54317|PNLIPRP2
1 MLPPWTLGLL LLATVRGKEV CYGQLGCFSD EKPWAGTLQR PVKLLPWSPE DIDTRFLLYT
61 NENPNNFQLI TGTEPDTIEA SNFQLDRKTR FIIHGFLDKA EDSWPSDMCK KMFEVEKVNC
121 ICVDWRHGSR AMYTQAVQNI RVVGAETAFL IQALSTQLGY SLEDVHVIGH SLGAHTAAEA
181 GRRLGGRVGR ITGLDPAGPC FQDEPEEVRL DPSDAVFVDV IHTDSSPIVP SLGFGMSQKV
241 GHLDFFPNGG KEMPGCKKNV LSTITDIDGI WEGIGGFVSC NHLRSFEYYS SSVLNPDGFL
301 GYPCASYDEF QESKCFPCPA EGCPKMGHYA DQFKGKTSAV EQTFFLNTGE SGNFTSWRYK
361 ISVTLSGKEK VNGYIRIALY GSNENSKQYE IFKGSLKPDA SHTCAIDVDF NVGKIQKVKF
421 LWNKRGINLS EPKLGASQIT VQSGEDGTEY NFCSSDTVEE NVLQSLYPCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PNLIPRP2 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.23
- Highest tissue expression
- 8,150 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 8,150 nTPM
- small intestine: 75 nTPM
- duodenum: 61 nTPM
- rectum: 17 nTPM
- stomach: 7.5 nTPM
- colon: 7 nTPM
Single-cell type
- pancreatic acinar cells: 2,695 nCPM
- enterocytes: 209 nCPM
- enteric transient amplifying cells: 30 nCPM
- pancreatic duct cells: 29 nCPM
- enteric stem cells: 29 nCPM
- colonocytes: 13 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- thalamus: 0.2 nTPM
- hypothalamus: 0.1 nTPM
- midbrain: 0.1 nTPM
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 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)
- 1.18
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.22
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
- cholesterol homeostasis
- fatty acid biosynthetic process
- high-density lipoprotein particle remodeling
- lipid digestion
- phosphatidylcholine catabolic process
- phospholipid catabolic process
- triglyceride catabolic process
- triglyceride metabolic process
- galactolipid catabolic process
Molecular functions
- calcium ion binding
- lipoprotein lipase activity
- monoacylglycerol lipase activity
- phospholipase A1 activity
- phospholipase activity
- triacylglycerol lipase activity
- galactolipase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PNLIPRP2 as an antibody target. Whether an autoantibody or antibody against PNLIPRP2 could matter depends on whether native PNLIPRP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PNLIPRP2 is annotated as secreted, so native PNLIPRP2 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label PNLIPRP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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