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MIRAGE
cholinergic receptor nicotinic beta 1 subunit

Summary
Gene Symbol
  • CHRNB1
Organism
Homo sapiens (human)
NCBI Gene
1140
PubChem
1140
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Cell membrane
  • Congenital myasthenic syndrome
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Ligand-gated ion channel
  • Phosphoprotein
  • Postsynaptic cell membrane
  • Receptor
  • Reference proteome
  • Signal
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
P11230
Annotation information from UniProt.
Gene Ontology (GO)
Displaying entries 1 - 5 of 16 in total
GO Term Evidence Code PMID
postsynaptic membrane organization
monoatomic cation transport
muscle contraction
signal transduction
chemical synaptic transmission
GO Hierarchy
Displaying entries 1 - 5 of 10 in total
GO Term Evidence Code PMID
transmembrane signaling receptor activity
protein binding
channel activity
ligand-gated monoatomic ion channel activity
acetylcholine receptor activity
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
OrthoDB (Group)
Group level
Eukaryota
Group Name
acetylcholine receptor subunit
Functional Category
  • E: Amino acid transport and metabolism
  • T: Signal transduction mechanisms
  • X: Mobilome: prophages, transposons
Displaying all 5 entries
Gene Ontology
excitatory postsynaptic potential
extracellular ligand-gated monoatomic ion channel activity
monoatomic ion channel activity
monoatomic ion transport
regulation of postsynaptic membrane potential
Displaying all 8 entries
InterPro
Neuronal acetylcholine receptor
Neurotransmitter-gated ion-channel ligand-binding domain superfamily
Neurotransmitter-gated ion-channel ligand-binding domain
Neurotransmitter-gated ion-channel transmembrane domain superfamily
Neurotransmitter-gated ion-channel transmembrane domain
Neurotransmitter-gated ion-channel, conserved site
Neurotransmitter-gated ion-channel
Nicotinic acetylcholine receptor
Disease
Disease Ontology
Displaying all 2 entries
DO ID Disease Name Source
DOID:0110680 congenital myasthenic syndrome 2C
DOID:0110681 congenital myasthenic syndrome 2A
Ortholog
Displaying entries 61 - 70 of 101 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
101614638 JACJA21157
101938098 CHRPI28831
101976363 ICTTR16575
102013271 CHILA16204
102125153 MACFA12895
102186994 CAPHI10382
102422849 MYOLU16338
102461595 PELSI05755
103034589 ASTMX06984
103242299 CHLSB05197
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025