Reference Gene

Gene name Alias Species Exons Type Paralogs EC number OMIM
CHRNB2 cholinergic receptor nicotinic beta 2 subunit EFNL3 , nAChRB2 Homo sapiens 7 protein-coding ZACN , HTR3B , HTR3A , CHRNA9 , HTR3C , HTR3D , HTR3E , CHRNA10 , CHRNG , CHRNB1 , CHRND , CHRNE , CHRNB4 , CHRNB3 , CHRNA5 , CHRNA3 , CHRNA6 , CHRNA4 , CHRNA1 , CHRNA2 , CHRFAM7A , CHRNA7 , GABRE , GABRG3 , GABRG1 , GABRG2 , GABRA2 , GABRA3 , GABRA5 , GABRA1 , GABRA4 , GABRA6 , GABRD , GABRQ , GABRP , GABRB1 , GABRB3 , GABRR2 , GABRR3 , GABRR1 , GABRB2 , GLRB , GLRA2 , GLRA1 , GLRA3 118507

Summary

Neuronal acetylcholine receptors are homo- or heteropentameric complexes composed of homologous alpha and beta subunits. They belong to a superfamily of ligand-gated ion channels which allow the flow of sodium and potassium across the plasma membrane in response to ligands such as acetylcholine and nicotine. This gene encodes one of several beta subunits. Mutations in this gene are associated with autosomal dominant nocturnal frontal lobe epilepsy. [provided by RefSeq, Jul 2008]

GeneOntology

Gene Loss events - CHRNB2 (1 results)

GL_ID Species Order Gene Loss Mechanism Loss Type Lineage Specific Citation
GL_317GVR Galeopterus variegatus Dermoptera LOF (frameshift, premature stop, ss) Full No 10.1093/icb/icy004