LILRA1
Leukocyte immunoglobulin-like receptor subfamily A member 1
Also known as: CD85i, LIR-6, LIR6, LIRA1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75019
- Gene
- LILRA1
- Ensembl
- ENSG00000104974
- Chromosome
- 19
- Canonical length
- 489 aa
- Protein class
- CD markers, Predicted membrane proteins
OverviewNCBI Gene
This gene encodes an activating member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein is predominantly expressed in B cells, interacts with major histocompatibility complex class I ligands, and contributes to the regulation of immune responses. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]
Canonical amino-acid sequenceUniProt
489 residues, UniProt reviewed canonical sequence.
>O75019|LILRA1
1 MTPIVTVLIC LRLSLGPRTH VQAGTLPKPT LWAEPGSVIT QGSPVTLWCQ GILETQEYRL
61 YREKKTAPWI TRIPQEIVKK GQFPIPSITW EHTGRYRCFY GSHTAGWSEP SDPLELVVTG
121 AYIKPTLSAL PSPVVTSGGN VTLHCVSQVA FGSFILCKEG EDEHPQCLNS QPRTHGWSRA
181 IFSVGPVSPS RRWSYRCYAY DSNSPHVWSL PSDLLELLVL GVSKKPSLSV QPGPIVAPGE
241 SLTLQCVSDV SYDRFVLYKE GERDFLQLPG PQPQAGLSQA NFTLGPVSRS YGGQYRCSGA
301 YNLSSEWSAP SDPLDILIAG QFRGRPFISV HPGPTVASGE NVTLLCQSWG PFHTFLLTKA
361 GAADAPLRLR SIHEYPKYQA EFPMSPVTSA HSGTYRCYGS LSSNPYLLSH PSDSLELMVS
421 GAAETLSPPQ NKSDSKAGAA NTLSPSQNKT ASHPQDYTVE NLIRMGIAGL VLVVLGILLF
481 EAQHSQRSLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LILRA1 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)
- 0.36
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- spleen: 13 nTPM
- appendix: 7.8 nTPM
- bone marrow: 2.5 nTPM
- lung: 2.1 nTPM
- urinary bladder: 2 nTPM
- spinal cord: 1.4 nTPM
Single-cell type
- microglia: 16 nCPM
- monocytes: 11 nCPM
- kupffer cells: 5.1 nCPM
- neutrophils: 4.3 nCPM
- macrophages: 2.9 nCPM
- cdc: 1.9 nCPM
Immune cell
- non-classical monocyte: 170 nTPM
- intermediate monocyte: 127 nTPM
- classical monocyte: 47 nTPM
- eosinophil: 36 nTPM
- neutrophil: 36 nTPM
- myeloid DC: 33 nTPM
Brain region
- white matter: 2.7 nTPM
- medulla oblongata: 2.1 nTPM
- spinal cord: 2 nTPM
- thalamus: 1.8 nTPM
- midbrain: 1.6 nTPM
- pons: 1.6 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)
- 1.61
- gnomAD pLI
- 0
- gnomAD missense Z
- -2.17
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adaptive immune response
- cell surface receptor signaling pathway
- defense response
- immune response-regulating signaling pathway
- interleukin-10-mediated signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads LILRA1 as an antibody target. Whether an autoantibody or antibody against LILRA1 could matter depends on whether native LILRA1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LILRA1 is annotated at the cell surface, where native LILRA1 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 LILRA1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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