BPIFA2
BPI fold-containing family A member 2
Also known as: bA49G10.1, BPIA2_HUMAN, C20orf70, PSP, SPLUNC2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96DR5
- Gene
- BPIFA2
- Ensembl
- ENSG00000131050
- Chromosome
- 20
- Canonical length
- 249 aa
- Protein class
- Predicted secreted proteins
- Secretome location
- Secreted to digestive system
OverviewNCBI Gene
This gene encodes a member of the palate, lung and nasal epithelium clone (Plunc) family of proteins. Members of this family have been proposed to play a role in the local antibacterial response in nose, mouth and upper respiratory pathways. The encoded soluble salivary protein binds bacterial lipopolysaccharide (LPS) and inhibits bacterial growth. This gene is present in a gene cluster on chromosome 20. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Canonical amino-acid sequenceUniProt
249 residues, UniProt reviewed canonical sequence.
>Q96DR5|BPIFA2
1 MLQLWKLVLL CGVLTGTSES LLDNLGNDLS NVVDKLEPVL HEGLETVDNT LKGILEKLKV
61 DLGVLQKSSA WQLAKQKAQE AEKLLNNVIS KLLPTNTDIF GLKISNSLIL DVKAEPIDDG
121 KGLNLSFPVT ANVTVAGPII GQIINLKASL DLLTAVTIET DPQTHQPVAV LGECASDPTS
181 ISLSLLDKHS QIINKFVNSV INTLKSTVSS LLQKEICPLI RIFIHSLDVN VIQQVVDNPQ
241 HKTQLQTLILocalizationUniProt · AlphaFold · HPA
Whether an antibody against BPIFA2 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)
- 0.4
- Highest tissue expression
- 6,453 nTPM
Expression across tissuesHPA
Tissue
- salivary gland: 6,453 nTPM
- epididymis: 4 nTPM
- pancreas: 3.7 nTPM
- testis: 1.1 nTPM
- heart muscle: 0.9 nTPM
- bone marrow: 0.4 nTPM
Single-cell type
- salivary acinar cells: 3,985 nCPM
- salivary myoepithelial cells: 995 nCPM
- respiratory ionocytes: 241 nCPM
- conjunctival goblet cells: 163 nCPM
- neutrophils: 104 nCPM
- salivary ionocytes: 100 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
- cerebral cortex: 0.1 nTPM
- hippocampal formation: 0.1 nTPM
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- choroid plexus: 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)
- 1.5
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.05
- DepMap mean gene effect
- 0.1
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Lipid-binding serum glycoprotein, N-terminal
- Bactericidal permeability-increasing protein, alpha/beta domain superfamily
- LBP / BPI / CETP family, N-terminal domain
- BPI fold-containing antibacterial protein
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads BPIFA2 as an antibody target. Whether an autoantibody or antibody against BPIFA2 could matter depends on whether native BPIFA2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BPIFA2 is annotated as secreted, so native BPIFA2 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 BPIFA2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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