PELI2
E3 ubiquitin-protein ligase pellino homolog 2
Also known as: PELI2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9HAT8
- Gene
- PELI2
- Ensembl
- ENSG00000139946
- Chromosome
- 14
- Canonical length
- 420 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Intermediate filaments,Centriolar satellite,Centrosome,Basal body,Cytosol
OverviewNCBI Gene
Predicted to enable protein-macromolecule adaptor activity and ubiquitin protein ligase activity. Acts upstream of or within positive regulation of MAPK cascade and positive regulation of protein phosphorylation. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
420 residues, UniProt reviewed canonical sequence.
>Q9HAT8|PELI2
1 MFSPGQEEHC APNKEPVKYG ELVVLGYNGA LPNGDRGRRK SRFALYKRPK ANGVKPSTVH
61 VISTPQASKA ISCKGQHSIS YTLSRNQTVV VEYTHDKDTD MFQVGRSTES PIDFVVTDTI
121 SGSQNTDEAQ ITQSTISRFA CRIVCDRNEP YTARIFAAGF DSSKNIFLGE KAAKWKNPDG
181 HMDGLTTNGV LVMHPRGGFT EESQPGVWRE ISVCGDVYTL RETRSAQQRG KLVESETNVL
241 QDGSLIDLCG ATLLWRTADG LFHTPTQKHI EALRQEINAA RPQCPVGLNT LAFPSINRKE
301 VVEEKQPWAY LSCGHVHGYH NWGHRSDTEA NERECPMCRT VGPYVPLWLG CEAGFYVDAG
361 PPTHAFTPCG HVCSEKSAKY WSQIPLPHGT HAFHAACPFC ATQLVGEQNC IKLIFQGPIDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PELI2 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)
- 0.27
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 27 nTPM
- thymus: 18 nTPM
- bone marrow: 18 nTPM
- retina: 14 nTPM
- stomach: 14 nTPM
- ovary: 13 nTPM
Single-cell type
- neutrophils: 1,063 nCPM
- pancreatic acinar cells: 709 nCPM
- neutrophil progenitors: 472 nCPM
- tuft cells: 450 nCPM
- pituicytes/fscs: 403 nCPM
- retinal ganglion cells: 379 nCPM
Immune cell
- neutrophil: 5.6 nTPM
- eosinophil: 2.4 nTPM
- classical monocyte: 1.9 nTPM
- myeloid DC: 1.3 nTPM
- intermediate monocyte: 1 nTPM
- basophil: 0.9 nTPM
Brain region
- cerebellum: 65 nTPM
- midbrain: 31 nTPM
- thalamus: 29 nTPM
- pons: 27 nTPM
- medulla oblongata: 26 nTPM
- white matter: 26 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)
- 0.41
- gnomAD pLI
- 0.83
- gnomAD missense Z
- 1.6
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of MAPK cascade
- positive regulation of protein phosphorylation
- protein polyubiquitination
- regulation of Toll signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PELI2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PELI2 as an antibody target. Whether an autoantibody or antibody against PELI2 could matter depends on whether native PELI2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PELI2 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 PELI2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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