| OPRM1 |
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| Identifiers |
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| Aliases | OPRM1, LMOR, M-OR-1, MOP, MOR, MOR1, OPRM, opioid receptor mu 1 |
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| External IDs | OMIM: 600018; MGI: 97441; HomoloGene: 37368; GeneCards: OPRM1; OMA:OPRM1 - orthologs |
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| Gene location (Human) |
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| | Chr. | Chromosome 6 (human) |
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| | Band | 6q25.2 | Start | 154,010,496 bp |
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| End | 154,246,867 bp |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 10 (mouse) |
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| | Band | 10 A1|10 1.85 cM | Start | 6,708,506 bp |
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| End | 6,988,198 bp |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - gonad
- testicle
- right hemisphere of cerebellum
- sperm
- left testis
- right testis
- prefrontal cortex
- Brodmann area 9
- nucleus accumbens
- hypothalamus
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| | Top expressed in | - medial habenular nucleus
- autonomic nerve plexus
- myenteric plexus
- Subplate
- spinal ganglia
- embryo
- nucleus of trigeminal nuclear complex
- greater petrosal nerve
- superior frontal gyrus
- granulocyte
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| | More reference expression data |
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| BioGPS | |
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| Gene ontology |
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| Molecular function | | | Cellular component | | | Biological process | | | Sources:Amigo / QuickGO |
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| Wikidata |
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The μ-opioid receptors (MOR) are a class of opioid receptors with a high affinity for enkephalins and beta-endorphin, but a low affinity for dynorphins. They are also referred to as μ(mu)-opioid peptide (MOP) receptors. The prototypical μ-opioid receptor agonist is morphine, the primary psychoactive alkaloid in opium and for which the receptor was named, with mu being the first letter of Morpheus, the compound's namesake in the original Greek. It is an inhibitory G-protein coupled receptor that activates the Gi alpha subunit, inhibiting adenylate cyclase activity, lowering cAMP levels.