Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1129
Gene name Gene Name - the full gene name approved by the HGNC.
Cholinergic receptor muscarinic 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CHRM2
Synonyms (NCBI Gene) Gene synonyms aliases
HM2
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q33
Summary Summary of gene provided in NCBI Entrez 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 to these receptors and includes cellular responses such as adenylate cycl
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017560 hsa-miR-335-5p Microarray 18185580
MIRT617798 hsa-miR-3140-3p HITS-CLIP 23824327
MIRT617797 hsa-miR-642a-5p HITS-CLIP 23824327
MIRT617796 hsa-miR-29b-2-5p HITS-CLIP 23824327
MIRT617795 hsa-miR-4755-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0005730 Component Nucleolus IDA
GO:0005794 Component Golgi apparatus IDA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IDA 24256733
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
118493 1951 ENSG00000181072
Protein
UniProt ID P08172
Protein name Muscarinic acetylcholine receptor M2
Protein function The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effec
PDB 3UON , 4MQS , 4MQT , 5YC8 , 5ZK3 , 5ZK8 , 5ZKB , 5ZKC , 6OIK , 6U1N , 7T8X , 7T90 , 7T94 , 7T96 , 8J8R , 8J97 , 8JAF
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 40 440 7 transmembrane receptor (rhodopsin family) Family
Sequence
Sequence length 466
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Calcium signaling pathway
cAMP signaling pathway
Neuroactive ligand-receptor interaction
PI3K-Akt signaling pathway
Cholinergic synapse
Regulation of actin cytoskeleton
  Muscarinic acetylcholine receptors
G alpha (i) signalling events
Cargo recognition for clathrin-mediated endocytosis
Clathrin-mediated endocytosis
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
cardiomyopathy Cardiomyopathy N/A N/A ClinVar
Dilated Cardiomyopathy Dilated Cardiomyopathy, Dominant N/A N/A ClinVar
Migraine with Aura Migraine with aura N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 34133324
Alzheimer Disease Associate 16181410
Antisocial Personality Disorder Associate 21883161
Arrhythmias Cardiac Associate 18451336
Asthma Associate 11325793, 22370858, 24430298
Atrial Fibrillation Associate 21617318
Atrioventricular Block Associate 18451336
Bipolar Disorder Associate 20351719
Carcinoma Renal Cell Inhibit 31862408
Cardiomyopathy Dilated Associate 18451336