CHRM4
Muscarinic acetylcholine receptor M4
Also known as: ACM4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P08173
- Gene
- CHRM4
- Ensembl
- ENSG00000180720
- Chromosome
- 11
- Canonical length
- 479 aa
- Protein class
- FDA approved drug targets, G-protein coupled receptors, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus
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, mouse studies link its function to adenylyl cyclase inhibition. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
479 residues, UniProt reviewed canonical sequence.
>P08173|CHRM4
1 MANFTPVNGS SGNQSVRLVT SSSHNRYETV EMVFIATVTG SLSLVTVVGN ILVMLSIKVN
61 RQLQTVNNYF LFSLACADLI IGAFSMNLYT VYIIKGYWPL GAVVCDLWLA LDYVVSNASV
121 MNLLIISFDR YFCVTKPLTY PARRTTKMAG LMIAAAWVLS FVLWAPAILF WQFVVGKRTV
181 PDNQCFIQFL SNPAVTFGTA IAAFYLPVVI MTVLYIHISL ASRSRVHKHR PEGPKEKKAK
241 TLAFLKSPLM KQSVKKPPPG EAAREELRNG KLEEAPPPAL PPPPRPVADK DTSNESSSGS
301 ATQNTKERPA TELSTTEATT PAMPAPPLQP RALNPASRWS KIQIVTKQTG NECVTAIEIV
361 PATPAGMRPA ANVARKFASI ARNQVRKKRQ MAARERKVTR TIFAILLAFI LTWTPYNVMV
421 LVNTFCQSCI PDTVWSIGYW LCYVNSTINP ACYALCNATF KKTFRHLLLC QYRNIGTARLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CHRM4 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)
- 0.43
- Highest tissue expression
- 14 nTPM
Expression across tissuesHPA
Tissue
- spleen: 14 nTPM
- small intestine: 5.8 nTPM
- cerebral cortex: 4.6 nTPM
- testis: 3.2 nTPM
- duodenum: 3 nTPM
- retina: 2.9 nTPM
Single-cell type
- goblet cells: 15 nCPM
- late spermatids: 10 nCPM
- late primary spermatocytes: 8 nCPM
- cone photoreceptor cells: 6.2 nCPM
- pancreatic islet cells: 5.8 nCPM
- neuroendocrine cells: 3.5 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- basal ganglia: 44 nTPM
- cerebral cortex: 14 nTPM
- hippocampal formation: 11 nTPM
- amygdala: 11 nTPM
- thalamus: 8.4 nTPM
- hypothalamus: 6.9 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)
- 0.27
- gnomAD pLI
- 0.97
- gnomAD missense Z
- 2.73
- DepMap mean gene effect
- -0.16
- DepMap dependency class
- selective
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
- cell surface receptor signaling pathway
- chemical synaptic transmission
- G protein-coupled acetylcholine receptor signaling pathway
- G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger
- regulation of locomotion
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CHRM4 as an antibody target. Whether an autoantibody or antibody against CHRM4 could matter depends on whether native CHRM4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CHRM4 is annotated at the cell surface, where native CHRM4 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 CHRM4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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