TRPV1
Transient receptor potential cation channel subfamily V member 1
Also known as: TRPV1_HUMAN, VR1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NER1
- Gene
- TRPV1
- Ensembl
- ENSG00000196689
- Chromosome
- 17
- Canonical length
- 839 aa
- Protein class
- FDA approved drug targets, Predicted membrane proteins, Transporters, Voltage-gated ion channels
- Quaternary structure
- Homotetramer
OverviewNCBI Gene
Capsaicin, the main pungent ingredient in hot chili peppers, elicits a sensation of burning pain by selectively activating sensory neurons that convey information about noxious stimuli to the central nervous system. The protein encoded by this gene is a receptor for capsaicin and is a non-selective cation channel that is structurally related to members of the TRP family of ion channels. This receptor is also activated by increases in temperature in the noxious range, suggesting that it functions as a transducer of painful thermal stimuli in vivo. Four transcript variants encoding the same protein, but with different 5' UTR sequence, have been described for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
839 residues, UniProt reviewed canonical sequence.
>Q8NER1|TRPV1
1 MKKWSSTDLG AAADPLQKDT CPDPLDGDPN SRPPPAKPQL STAKSRTRLF GKGDSEEAFP
61 VDCPHEEGEL DSCPTITVSP VITIQRPGDG PTGARLLSQD SVAASTEKTL RLYDRRSIFE
121 AVAQNNCQDL ESLLLFLQKS KKHLTDNEFK DPETGKTCLL KAMLNLHDGQ NTTIPLLLEI
181 ARQTDSLKEL VNASYTDSYY KGQTALHIAI ERRNMALVTL LVENGADVQA AAHGDFFKKT
241 KGRPGFYFGE LPLSLAACTN QLGIVKFLLQ NSWQTADISA RDSVGNTVLH ALVEVADNTA
301 DNTKFVTSMY NEILMLGAKL HPTLKLEELT NKKGMTPLAL AAGTGKIGVL AYILQREIQE
361 PECRHLSRKF TEWAYGPVHS SLYDLSCIDT CEKNSVLEVI AYSSSETPNR HDMLLVEPLN
421 RLLQDKWDRF VKRIFYFNFL VYCLYMIIFT MAAYYRPVDG LPPFKMEKTG DYFRVTGEIL
481 SVLGGVYFFF RGIQYFLQRR PSMKTLFVDS YSEMLFFLQS LFMLATVVLY FSHLKEYVAS
541 MVFSLALGWT NMLYYTRGFQ QMGIYAVMIE KMILRDLCRF MFVYIVFLFG FSTAVVTLIE
601 DGKNDSLPSE STSHRWRGPA CRPPDSSYNS LYSTCLELFK FTIGMGDLEF TENYDFKAVF
661 IILLLAYVIL TYILLLNMLI ALMGETVNKI AQESKNIWKL QRAITILDTE KSFLKCMRKA
721 FRSGKLLQVG YTPDGKDDYR WCFRVDEVNW TTWNTNVGII NEDPGNCEGV KRTLSFSLRS
781 SRVSGRHWKN FALVPLLREA SARDRQSAQP EEVYLRQFSG SLKPEDAEVF KSPAASGEKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TRPV1 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
- 6
- Mean surface accessibility (rSASA)
- 0.38
- Highest tissue expression
- 22 nTPM
Expression across tissuesHPA
Tissue
- liver: 22 nTPM
- cerebellum: 12 nTPM
- retina: 12 nTPM
- ovary: 9.4 nTPM
- small intestine: 7.7 nTPM
- cervix: 7.6 nTPM
Single-cell type
- rod photoreceptor cells: 26 nCPM
- myonuclei: 26 nCPM
- proximal tubule cells: 25 nCPM
- myosatellite cells: 22 nCPM
- astrocytes: 20 nCPM
- cone photoreceptor cells: 19 nCPM
Immune cell
- naive CD8 T-cell: 0.3 nTPM
- eosinophil: 0.2 nTPM
- plasmacytoid DC: 0.2 nTPM
- basophil: 0.1 nTPM
- classical monocyte: 0.1 nTPM
- MAIT T-cell: 0.1 nTPM
Brain region
- white matter: 15 nTPM
- midbrain: 11 nTPM
- basal ganglia: 10 nTPM
- cerebellum: 9.3 nTPM
- cerebral cortex: 9.3 nTPM
- thalamus: 8.9 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TRPV1.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 182 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- See cases
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)
- 1.08
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.47
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
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
- behavioral response to pain
- calcium ion import across plasma membrane
- calcium ion transmembrane transport
- cell surface receptor signaling pathway
- cellular response to acidic pH
- cellular response to alkaloid
- cellular response to ATP
- cellular response to heat
- chemosensory behavior
- detection of chemical stimulus involved in sensory perception of pain
- detection of temperature stimulus involved in sensory perception of pain
- detection of temperature stimulus involved in thermoception
- diet induced thermogenesis
- fever generation
- lipid metabolic process
- negative regulation of transcription by RNA polymerase II
- peptide secretion
- protein homotetramerization
- sensory perception of mechanical stimulus
- sensory perception of taste
- smooth muscle contraction involved in micturition
- thermoception
- response to capsazepine
Molecular functions
- ATP binding
- calcium channel activity
- calmodulin binding
- excitatory extracellular ligand-gated monoatomic ion channel activity
- extracellular ligand-gated monoatomic ion channel activity
- intracellularly gated calcium channel activity
- metal ion binding
- phosphatidylinositol binding
- phosphoprotein binding
- transmembrane signaling receptor activity
- voltage-gated calcium channel activity
- temperature-gated ion channel activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TRPV1 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 TRPV1 as an antibody target. Whether an autoantibody or antibody against TRPV1 could matter depends on whether native TRPV1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TRPV1 is annotated at the cell surface, where native TRPV1 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 TRPV1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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