CHRM5
Muscarinic acetylcholine receptor M5
Also known as: ACM5_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P08912
- Gene
- CHRM5
- Ensembl
- ENSG00000184984
- Chromosome
- 15
- Canonical length
- 532 aa
- Protein class
- FDA approved drug targets, G-protein coupled receptors, Predicted intracellular proteins, Predicted membrane proteins
OverviewNCBI Gene
The muscarinic cholinergic receptors belong to a larger family of G protein-coupled receptors. The functional diversity of these receptors is defined by the binding of acetylcholine and includes cellular responses such as adenylate cyclase inhibition, phosphoinositide degeneration, and potassium channel mediation. Muscarinic receptors influence many effects of acetylcholine in the central and peripheral nervous system. The clinical implications of this receptor are unknown; however, stimulation of this receptor is known to increase cyclic AMP levels. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
532 residues, UniProt reviewed canonical sequence.
>P08912|CHRM5
1 MEGDSYHNAT TVNGTPVNHQ PLERHRLWEV ITIAAVTAVV SLITIVGNVL VMISFKVNSQ
61 LKTVNNYYLL SLACADLIIG IFSMNLYTTY ILMGRWALGS LACDLWLALD YVASNASVMN
121 LLVISFDRYF SITRPLTYRA KRTPKRAGIM IGLAWLISFI LWAPAILCWQ YLVGKRTVPL
181 DECQIQFLSE PTITFGTAIA AFYIPVSVMT ILYCRIYRET EKRTKDLADL QGSDSVTKAE
241 KRKPAHRALF RSCLRCPRPT LAQRERNQAS WSSSRRSTST TGKPSQATGP SANWAKAEQL
301 TTCSSYPSSE DEDKPATDPV LQVVYKSQGK ESPGEEFSAE ETEETFVKAE TEKSDYDTPN
361 YLLSPAAAHR PKSQKCVAYK FRLVVKADGN QETNNGCHKV KIMPCPFPVA KEPSTKGLNP
421 NPSHQMTKRK RVVLVKERKA AQTLSAILLA FIITWTPYNI MVLVSTFCDK CVPVTLWHLG
481 YWLCYVNSTV NPICYALCNR TFRKTFKMLL LCRWKKKKVE EKLYWQGNSK LPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CHRM5 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)
- 0.47
- Highest tissue expression
- 7.1 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 7.1 nTPM
- midbrain: 2.6 nTPM
- hypothalamus: 1.9 nTPM
- placenta: 1.4 nTPM
- testis: 1.3 nTPM
- hippocampal formation: 1.2 nTPM
Single-cell type
- epicardial cells: 205 nCPM
- oligodendrocytes: 89 nCPM
- cardiomyocytes: 78 nCPM
- retinal bipolar cells: 69 nCPM
- adipocytes: 61 nCPM
- other brain neurons: 44 nCPM
Immune cell
- basophil: 0.4 nTPM
- neutrophil: 0.4 nTPM
- plasmacytoid DC: 0.2 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- hypothalamus: 43 nTPM
- white matter: 30 nTPM
- medulla oblongata: 23 nTPM
- midbrain: 22 nTPM
- pons: 22 nTPM
- thalamus: 16 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)
- 0.74
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.2
- DepMap mean gene effect
- -0.03
- 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
- chemical synaptic transmission
- dopamine transport
- G protein-coupled acetylcholine receptor signaling pathway
- G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger
- gastric acid secretion
- regulation of phosphatidylinositol dephosphorylation
- transmission of nerve impulse
Molecular functions
- G protein-coupled acetylcholine receptor activity
- phosphatidylinositol-4,5-bisphosphate phospholipase C activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CHRM5 as an antibody target. Whether an autoantibody or antibody against CHRM5 could matter depends on whether native CHRM5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CHRM5 is annotated at the cell surface, where native CHRM5 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 CHRM5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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