LILRA6
Leukocyte immunoglobulin-like receptor subfamily A member 6
Also known as: CD85b, ILT8, LILRB6, LIRA6_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6PI73
- Gene
- LILRA6
- Ensembl
- ENSG00000244482
- Chromosome
- 19
- Canonical length
- 481 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Plasma membrane,Cytosol
OverviewNCBI Gene
Predicted to enable inhibitory MHC class I receptor activity. Predicted to be involved in cytokine-mediated signaling pathway and immune response-regulating signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
481 residues, UniProt reviewed canonical sequence.
>Q6PI73|LILRA6
1 MTPALTALLC LGLSLGPRTR VQAGPFPKPT LWAEPGSVIS WGSPVTIWCQ GSLEAQEYQL
61 DKEGSPEPLD RNNPLEPKNK ARFSIPSMTQ HHAGRYRCHY YSSAGWSEPS DPLELVMTGF
121 YNKPTLSALP SPVVASGGNM TLRCGSQKGY HHFVLMKEGE HQLPRTLDSQ QLHSGGFQAL
181 FPVGPVTPSH RWRFTCYYYY TNTPRVWSHP SDPLEILPSG VSRKPSLLTL QGPVLAPGQS
241 LTLQCGSDVG YDRFVLYKEG ERDFLQRPGQ QPQAGLSQAN FTLGPVSPSH GGQYRCYGAH
301 NLSSEWSAPS DPLNILMAGQ IYDTVSLSAQ PGPTVASGEN VTLLCQSRGY FDTFLLTKEG
361 AAHPPLRLRS MYGAHKYQAE FPMSPVTSAH AGTYRCYGSY SSNPHLLSFP SEPLELMVSG
421 HSGGSSLPPT GPPSTPASHA KDYTVENLIR MGMAGLVLVF LGILLFEAQH SQRNPQDAAG
481 RLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LILRA6 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)
- 0.35
- Highest tissue expression
- 16 nTPM
Expression across tissuesHPA
Tissue
- spleen: 16 nTPM
- lung: 8.6 nTPM
- adipose tissue: 3.1 nTPM
- blood vessel: 1.9 nTPM
- bone marrow: 1.6 nTPM
- appendix: 1.5 nTPM
Single-cell type
- monocytes: 3.2 nCPM
- neutrophils: 2 nCPM
- macrophages: 1 nCPM
- cdc: 0.7 nCPM
- microglia: 0.6 nCPM
- monocyte progenitors: 0.3 nCPM
Immune cell
- neutrophil: 8.4 nTPM
- intermediate monocyte: 3.9 nTPM
- classical monocyte: 3.5 nTPM
- non-classical monocyte: 0.9 nTPM
- total PBMC: 0.9 nTPM
- myeloid DC: 0.2 nTPM
Brain region
- thalamus: 0.4 nTPM
- cerebral cortex: 0.2 nTPM
- white matter: 0.2 nTPM
- choroid plexus: 0.1 nTPM
- pons: 0.1 nTPM
- amygdala: 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)
- 0.91
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.43
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
- adaptive immune response
- cytokine-mediated signaling pathway
- immune response-regulating signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Immunoglobulin subtype 2
- Immunoglobulin domain subtype
- Immunoglobulin-like domain
- Immunoglobulin-like beta-sandwich domain
- Immunoglobulin-like fold
- Alpha-1B-glycoprotein/leukocyte immunoglobulin-like receptor
- Immunoglobulin-like domain superfamily
- Immunoglobulin-like Receptors in Immune Regulation
- Immunoglobulin domain
- Immunoglobulin domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads LILRA6 as an antibody target. Whether an autoantibody or antibody against LILRA6 could matter depends on whether native LILRA6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LILRA6 is annotated at the cell surface, where native LILRA6 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 LILRA6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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