BTNL3
Butyrophilin-like protein 3
Also known as: BTN9.1, BTNL3_HUMAN, BTNLR
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6UXE8
- Gene
- BTNL3
- Ensembl
- ENSG00000168903
- Chromosome
- 5
- Canonical length
- 466 aa
- Protein class
- Predicted membrane proteins
OverviewNCBI Gene
Predicted to enable signaling receptor binding activity. Predicted to be involved in T cell receptor signaling pathway and regulation of cytokine production. Predicted to be located in membrane. Predicted to be active in external side of plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
466 residues, UniProt reviewed canonical sequence.
>Q6UXE8|BTNL3
1 MAFVLILVLS FYELVSGQWQ VTGPGKFVQA LVGEDAVFSC SLFPETSAEA MEVRFFRNQF
61 HAVVHLYRDG EDWESKQMPQ YRGRTEFVKD SIAGGRVSLR LKNITPSDIG LYGCWFSSQI
121 YDEEATWELR VAALGSLPLI SIVGYVDGGI QLLCLSSGWF PQPTAKWKGP QGQDLSSDSR
181 ANADGYSLYD VEISIIVQEN AGSILCSIHL AEQSHEVESK VLIGETFFQP SPWRLASILL
241 GLLCGALCGV VMGMIIVFFK SKGKIQAELD WRRKHGQAEL RDARKHAVEV TLDPETAHPK
301 LCVSDLKTVT HRKAPQEVPH SEKRFTRKSV VASQGFQAGK HYWEVDVGQN VGWYVGVCRD
361 DVDRGKNNVT LSPNNGYWVL RLTTEHLYFT FNPHFISLPP STPPTRVGVF LDYEGGTISF
421 FNTNDQSLIY TLLTCQFEGL LRPYIQHAMY DEEKGTPIFI CPVSWGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BTNL3 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)
- 0.3
- Highest tissue expression
- 109 nTPM
Expression across tissuesHPA
Tissue
- duodenum: 109 nTPM
- small intestine: 76 nTPM
- colon: 24 nTPM
- rectum: 23 nTPM
- stomach: 1.6 nTPM
- gallbladder: 1.5 nTPM
Single-cell type
- enterocytes: 264 nCPM
- colonocytes: 135 nCPM
- goblet cells: 96 nCPM
- enteric transient amplifying cells: 52 nCPM
- paneth cells: 43 nCPM
- enteric stem cells: 28 nCPM
Immune cell
- neutrophil: 22 nTPM
- classical monocyte: 0.1 nTPM
- basophil: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebral cortex: 0.2 nTPM
- pons: 0.2 nTPM
- amygdala: 0.1 nTPM
- hypothalamus: 0.1 nTPM
- medulla oblongata: 0.1 nTPM
- midbrain: 0.1 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)
- 0.85
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.68
- DepMap mean gene effect
- 0.05
- DepMap dependency class
- none
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- B30.2/SPRY domain
- Immunoglobulin domain subtype
- SPRY domain
- Butyrophylin-like, SPRY domain
- SPRY-associated
- Immunoglobulin-like domain
- Immunoglobulin V-set domain
- Concanavalin A-like lectin/glucanase domain superfamily
- Immunoglobulin-like fold
- Immunoglobulin-like domain superfamily
- B30.2/SPRY domain superfamily
- BTN/MOG-like
- Butyrophilin subfamily 3 member A2-like, Ig-C domain
- SPRY domain
- Immunoglobulin V-set domain
- SPRY-associated domain
- Butyrophilin subfamily 3 member A2-like, Ig-C domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads BTNL3 as an antibody target. Whether an autoantibody or antibody against BTNL3 could matter depends on whether native BTNL3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BTNL3 is annotated at the cell surface, where native BTNL3 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 BTNL3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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