TP53I11
Tumor protein p53-inducible protein 11
Also known as: P5I11_HUMAN, PIG11
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O14683
- Gene
- TP53I11
- Ensembl
- ENSG00000175274
- Chromosome
- 11
- Canonical length
- 189 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Endoplasmic reticulum,Golgi apparatus,Acrosome,Principal piece
OverviewNCBI Gene
Predicted to be involved in negative regulation of cell population proliferation. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
189 residues, UniProt reviewed canonical sequence.
>O14683|TP53I11
1 MAAKQPPPLM KKHSQTDLVS RLKTRKILGV GGEDDDGEVH RSKISQVLGN EIKFTIREPL
61 GLRVWQFVSA VLFSGIAIMA LAFPDQLYDA VFDGAQVTSK TPIRLYGGAL LSISLIMWNA
121 LYTAEKVIIR WTLLTEACYF GVQFLVVTAT LAETGLMSLG ILLLLVSRLL FVVISIYYYY
181 QVGRRPKKALocalizationUniProt · AlphaFold · HPA
Whether an antibody against TP53I11 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 4
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 72 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 72 nTPM
- heart muscle: 68 nTPM
- cerebellum: 63 nTPM
- breast: 60 nTPM
- spleen: 58 nTPM
- blood vessel: 50 nTPM
Single-cell type
- late spermatids: 958 nCPM
- cardiomyocytes: 201 nCPM
- early spermatids: 152 nCPM
- neutrophils: 90 nCPM
- salivary ionocytes: 81 nCPM
- cytotrophoblasts: 75 nCPM
Immune cell
- neutrophil: 41 nTPM
- plasmacytoid DC: 25 nTPM
- non-classical monocyte: 21 nTPM
- naive B-cell: 8.4 nTPM
- memory B-cell: 8.1 nTPM
- NK-cell: 8.1 nTPM
Brain region
- amygdala: 90 nTPM
- cerebellum: 88 nTPM
- midbrain: 69 nTPM
- hypothalamus: 61 nTPM
- cerebral cortex: 61 nTPM
- pons: 56 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TP53I11.
Disease | ImmuneIEDB
Conditions an epitope on TP53I11 was assayed in.
- chronic lymphocytic leukemia T cell
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)
- 0.76
- gnomAD pLI
- 0.31
- gnomAD missense Z
- 1.82
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- none
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
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Tumor protein p53-inducible protein 11
- Tumour protein p53-inducible protein 11
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TP53I11 as an antibody target. Whether an autoantibody or antibody against TP53I11 could matter depends on whether native TP53I11 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TP53I11 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 TP53I11 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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