TIGIT
T-cell immunoreceptor with Ig and ITIM domains
Also known as: DKFZp667A205, FLJ39873, TIGIT_HUMAN, VSIG9, VSTM3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q495A1
- Gene
- TIGIT
- Ensembl
- ENSG00000181847
- Chromosome
- 3
- Canonical length
- 244 aa
- Protein class
- Predicted membrane proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a member of the PVR (poliovirus receptor) family of immunoglobin proteins. The product of this gene is expressed on several classes of T cells including follicular B helper T cells (TFH). The protein has been shown to bind PVR with high affinity; this binding is thought to assist interactions between TFH and dendritic cells to regulate T cell dependent B cell responses.[provided by RefSeq, Sep 2009]
Canonical amino-acid sequenceUniProt
244 residues, UniProt reviewed canonical sequence.
>Q495A1|TIGIT
1 MRWCLLLIWA QGLRQAPLAS GMMTGTIETT GNISAEKGGS IILQCHLSST TAQVTQVNWE
61 QQDQLLAICN ADLGWHISPS FKDRVAPGPG LGLTLQSLTV NDTGEYFCIY HTYPDGTYTG
121 RIFLEVLESS VAEHGARFQI PLLGAMAATL VVICTAVIVV VALTRKKKAL RIHSVEGDLR
181 RKSAGQEEWS PSAPSPPGSC VQAEAAPAGL CGEQRGEDCA ELHDYFNVLS YRSLGNCSFF
241 TETGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TIGIT 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)
- 0.5
- Highest tissue expression
- 36 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 36 nTPM
- tonsil: 19 nTPM
- spleen: 14 nTPM
- appendix: 11 nTPM
- thymus: 8.5 nTPM
- small intestine: 4.8 nTPM
Single-cell type
- t-cells: 96 nCPM
- nk-cells: 59 nCPM
- epicardial cells: 14 nCPM
- plasma cells: 9.7 nCPM
- cardiomyocytes: 8.2 nCPM
- endometrial stromal cells: 4.7 nCPM
Immune cell
- T-reg: 196 nTPM
- memory CD8 T-cell: 90 nTPM
- memory CD4 T-cell: 49 nTPM
- naive CD8 T-cell: 40 nTPM
- gdT-cell: 30 nTPM
- total PBMC: 22 nTPM
Brain region
- thalamus: 3.6 nTPM
- cerebral cortex: 3.5 nTPM
- white matter: 3.4 nTPM
- medulla oblongata: 3.1 nTPM
- pons: 3 nTPM
- basal ganglia: 2.9 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)
- 1.05
- gnomAD pLI
- 0.02
- gnomAD missense Z
- -0.04
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- none
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
- negative regulation of interleukin-12 production
- negative regulation of natural killer cell mediated cytotoxicity
- negative regulation of T cell activation
- positive regulation of interleukin-10 production
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Immunoglobulin domain subtype
- Immunoglobulin-like domain
- Immunoglobulin V-set domain
- Immunoglobulin-like fold
- Immunoglobulin-like domain superfamily
- Immunoglobulin V-set domain
- T-cell immunoglobulin and ITIM domain receptor
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TIGIT 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 TIGIT as an antibody target. Whether an autoantibody or antibody against TIGIT could matter depends on whether native TIGIT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TIGIT is annotated at the cell surface, where native TIGIT 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 TIGIT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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