PILRA
Paired immunoglobulin-like type 2 receptor alpha
Also known as: FDF03, PILRA_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UKJ1
- Gene
- PILRA
- Ensembl
- ENSG00000085514
- Chromosome
- 7
- Canonical length
- 303 aa
- Protein class
- Predicted membrane proteins, Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
Cell signaling pathways rely on a dynamic interaction between activating and inhibiting processes. SHP-1-mediated dephosphorylation of protein tyrosine residues is central to the regulation of several cell signaling pathways. Two types of inhibitory receptor superfamily members are immunoreceptor tyrosine-based inhibitory motif (ITIM)-bearing receptors and their non-ITIM-bearing, activating counterparts. Control of cell signaling via SHP-1 is thought to occur through a balance between PILRalpha-mediated inhibition and PILRbeta-mediated activation. These paired immunoglobulin-like receptor genes are located in a tandem head-to-tail orientation on chromosome 7. This particular gene encodes the ITIM-bearing member of the receptor pair, which functions in the inhibitory role. Alternative splicing has been observed at this locus and three variants, each encoding a distinct isoform, are described. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
303 residues, UniProt reviewed canonical sequence.
>Q9UKJ1|PILRA
1 MGRPLLLPLL PLLLPPAFLQ PSGSTGSGPS YLYGVTQPKH LSASMGGSVE IPFSFYYPWE
61 LATAPDVRIS WRRGHFHRQS FYSTRPPSIH KDYVNRLFLN WTEGQKSGFL RISNLQKQDQ
121 SVYFCRVELD TRSSGRQQWQ SIEGTKLSIT QAVTTTTQRP SSMTTTWRLS STTTTTGLRV
181 TQGKRRSDSW HISLETAVGV AVAVTVLGIM ILGLICLLRW RRRKGQQRTK ATTPAREPFQ
241 NTEEPYENIR NEGQNTDPKL NPKDDGIVYA SLALSSSTSP RAPPSHRPLK SPQNETLYSV
301 LKALocalizationUniProt · AlphaFold · HPA
Whether an antibody against PILRA 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.54
- Highest tissue expression
- 36 nTPM
Expression across tissuesHPA
Tissue
- appendix: 36 nTPM
- spleen: 30 nTPM
- lung: 29 nTPM
- bone marrow: 24 nTPM
- cerebellum: 24 nTPM
- urinary bladder: 17 nTPM
Single-cell type
- neutrophils: 1,383 nCPM
- monocytes: 226 nCPM
- microglia: 148 nCPM
- endometrial glandular cells: 119 nCPM
- decidual stromal cells: 100 nCPM
- macrophages: 98 nCPM
Immune cell
- neutrophil: 1,664 nTPM
- non-classical monocyte: 1,151 nTPM
- intermediate monocyte: 863 nTPM
- classical monocyte: 585 nTPM
- total PBMC: 354 nTPM
- basophil: 318 nTPM
Brain region
- white matter: 26 nTPM
- medulla oblongata: 19 nTPM
- cerebellum: 18 nTPM
- pons: 15 nTPM
- cerebral cortex: 14 nTPM
- thalamus: 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)
- 1.6
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.45
- DepMap mean gene effect
- -0.14
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PILRA 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 PILRA as an antibody target. Whether an autoantibody or antibody against PILRA could matter depends on whether native PILRA is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PILRA is annotated at the cell surface, where native PILRA is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label PILRA as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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