PIP
Prolactin-inducible protein
Also known as: BRST-2, GCDFP-15, GCDFP15, GPIP4, PIP_HUMAN, SABP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P12273
- Gene
- PIP
- Ensembl
- ENSG00000159763
- Chromosome
- 7
- Canonical length
- 146 aa
- Protein class
- Plasma proteins, Predicted secreted proteins
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
Enables IgG binding activity; aspartic-type endopeptidase activity; and identical protein binding activity. Involved in several processes, including detection of chemical stimulus involved in sensory perception of bitter taste; negative regulation of T cell apoptotic process; and proteolysis. Located in extracellular space and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
146 residues, UniProt reviewed canonical sequence.
>P12273|PIP
1 MRLLQLLFRA SPATLLLVLC LQLGANKAQD NTRKIIIKNF DIPKSVRPND EVTAVLAVQT
61 ELKECMVVKT YLISSIPLQG AFNYKYTACL CDDNPKTFYW DFYTNRTVQI AAVVDVIREL
121 GICPDDAAVI PIKNNRFYTI EILKVELocalizationUniProt · AlphaFold · HPA
Whether an antibody against PIP 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)
- 0.37
- Highest tissue expression
- 17,175 nTPM
Expression across tissuesHPA
Tissue
- salivary gland: 17,175 nTPM
- breast: 3,247 nTPM
- seminal vesicle: 2,949 nTPM
- skin: 183 nTPM
- prostate: 28 nTPM
- pancreas: 20 nTPM
Single-cell type
- lacrimal acinar cells: 23,034 nCPM
- salivary acinar cells: 5,978 nCPM
- breast hormone-responsive cells: 1,898 nCPM
- salivary myoepithelial cells: 1,045 nCPM
- submucosal glandular cells: 671 nCPM
- salivary duct cells: 253 nCPM
Immune cell
- naive B-cell: 0.5 nTPM
- memory B-cell: 0.4 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- white matter: 26 nTPM
- medulla oblongata: 22 nTPM
- pons: 16 nTPM
- basal ganglia: 13 nTPM
- thalamus: 13 nTPM
- hypothalamus: 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)
- 1.69
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.19
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- detection of chemical stimulus involved in sensory perception of bitter taste
- negative regulation of T cell apoptotic process
- positive regulation of gene expression
- proteolysis
- regulation of immune system process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Immunoglobulin-like fold
- Immunoglobulin E-set
- Prolactin-inducible protein
- Seminal vesicle autoantigen (SVA)
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PIP 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 PIP as an antibody target. Whether an autoantibody or antibody against PIP could matter depends on whether native PIP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PIP is annotated as secreted, so native PIP 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 PIP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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