Genomics England
GMS Panels
Panels
Genes and Entities

CHRNB1

cholinergic receptor nicotinic beta 1 subunit
OMIM: 100710
PanelMode of inheritanceDetails
4 panels
Green
in Arthrogryposis
R-numbers: R83
Signed-off version 5.21
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Congenital Myasthenic Syndrome, Dominant/Recessive, Myasthenic syndrome, slow-channel congenital, 601462
Green
in Congenital myaesthenic syndrome
Component of the following Super Panels:
  • - Hypotonic infant
  • - Other rare neuromuscular disorders
R-numbers: R80
Signed-off version 4.5
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
?Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency, OMIM:616314, Myasthenic syndrome, congenital, 2A, slow-channel, OMIM:616313
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
CHRNB1-related congenital myaesthenia, biallelic, OMIM:616314, CHRNB1-related congenital myaesthenia, monoallelic, OMIM:616313
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 3.122
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Myasthenic syndrome, congenital, 2A, slow-channel, 616313, ?Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency, 616314