OPRM1
Mu-type opioid receptor
Also known as: MOP, MOR1, OPRM_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P35372
- Gene
- OPRM1
- Ensembl
- ENSG00000112038
- Chromosome
- 6
- Canonical length
- 400 aa
- Protein class
- FDA approved drug targets, G-protein coupled receptors, Human disease related genes, Predicted membrane proteins, Transporters
- Quaternary structure
- Homooligomer
OverviewNCBI Gene
This gene encodes one of at least three opioid receptors in humans; the mu opioid receptor (MOR). The MOR is the principal target of endogenous opioid peptides and opioid analgesic agents such as beta-endorphin and enkephalins. The MOR also has an important role in dependence to other drugs of abuse, such as nicotine, cocaine, and alcohol via its modulation of the dopamine system. The NM_001008503.2:c.118A>G allele has been associated with opioid and alcohol addiction and variations in pain sensitivity but evidence for it having a causal role is conflicting. Multiple transcript variants encoding different isoforms have been found for this gene. Though the canonical MOR belongs to the superfamily of 7-transmembrane-spanning G-protein-coupled receptors some isoforms of this gene have only 6 transmembrane domains. [provided by RefSeq, Oct 2013]
Canonical amino-acid sequenceUniProt
400 residues, UniProt reviewed canonical sequence.
>P35372|OPRM1
1 MDSSAAPTNA SNCTDALAYS SCSPAPSPGS WVNLSHLDGN LSDPCGPNRT DLGGRDSLCP
61 PTGSPSMITA ITIMALYSIV CVVGLFGNFL VMYVIVRYTK MKTATNIYIF NLALADALAT
121 STLPFQSVNY LMGTWPFGTI LCKIVISIDY YNMFTSIFTL CTMSVDRYIA VCHPVKALDF
181 RTPRNAKIIN VCNWILSSAI GLPVMFMATT KYRQGSIDCT LTFSHPTWYW ENLLKICVFI
241 FAFIMPVLII TVCYGLMILR LKSVRMLSGS KEKDRNLRRI TRMVLVVVAV FIVCWTPIHI
301 YVIIKALVTI PETTFQTVSW HFCIALGYTN SCLNPVLYAF LDENFKRCFR EFCIPTSSNI
361 EQQNSTRIRQ NTRDHPSTAN TVDRTNHQLE NLEAETAPLPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against OPRM1 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
- 7
- Mean surface accessibility (rSASA)
- 0.38
- Highest tissue expression
- 4.4 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 4.4 nTPM
- testis: 2.6 nTPM
- basal ganglia: 1.4 nTPM
- hypothalamus: 1.3 nTPM
- esophagus: 1 nTPM
- retina: 0.9 nTPM
Single-cell type
- microglia: 152 nCPM
- adrenal medulla cells: 106 nCPM
- brain inhibitory neurons: 102 nCPM
- other brain neurons: 100 nCPM
- brain excitatory neurons: 93 nCPM
- late spermatids: 77 nCPM
Immune cell
- basophil: 1.1 nTPM
- neutrophil: 0.7 nTPM
- NK-cell: 0.4 nTPM
- plasmacytoid DC: 0.4 nTPM
- eosinophil: 0.3 nTPM
- MAIT T-cell: 0.3 nTPM
Brain region
- thalamus: 42 nTPM
- cerebellum: 38 nTPM
- midbrain: 30 nTPM
- cerebral cortex: 27 nTPM
- basal ganglia: 26 nTPM
- hypothalamus: 25 nTPM
ReferencesPubMed · IEDB
Publications for OPRM1 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
1 publication
- Autoantibodies against muscarinic cholinergic receptor in chronic fatigue syndrome.
2003 · Int J Mol Med · RCR 1.9 · 79 citations
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
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)
- 1.31
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.62
- 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
- adenylate cyclase-inhibiting G protein-coupled acetylcholine receptor signaling pathway
- adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway
- behavioral response to ethanol
- G protein-coupled opioid receptor signaling pathway
- G protein-coupled receptor signaling pathway
- G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger
- negative regulation of cell population proliferation
- negative regulation of cytosolic calcium ion concentration
- negative regulation of nitric oxide biosynthetic process
- neuropeptide signaling pathway
- phospholipase C-activating G protein-coupled receptor signaling pathway
- positive regulation of ERK1 and ERK2 cascade
- positive regulation of neurogenesis
- regulation of cellular response to stress
- regulation of NMDA receptor activity
- sensory perception
- sensory perception of pain
- negative regulation of Wnt protein secretion
Molecular functions
- G protein-coupled receptor activity
- G-protein alpha-subunit binding
- G-protein beta-subunit binding
- neuropeptide binding
- voltage-gated calcium channel activity
- beta-endorphin receptor activity
- morphine receptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of OPRM1 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 OPRM1 as an antibody target. Whether an autoantibody or antibody against OPRM1 could matter depends on whether native OPRM1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
OPRM1 is annotated at the cell surface, where native OPRM1 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 OPRM1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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