Gene: CHRNB1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1140
Gene Symbol: CHRNB1
CHRNB1 		0.600 GeneticVariation disease CLINVAR Whole exome sequencing diagnosis of inborn errors of metabolism and other disorders in United Arab Emirates. 27391121 2016
Entrez Id: 1140
Gene Symbol: CHRNB1
CHRNB1 		0.600 GeneticVariation disease UNIPROT Mutations Causing Slow-Channel Myasthenia Reveal That a Valine Ring in the Channel Pore of Muscle AChR is Optimized for Stabilizing Channel Gating. 27375219 2016
Entrez Id: 1140
Gene Symbol: CHRNB1
CHRNB1 		0.600 GeneticVariation disease CLINVAR Mutations Causing Slow-Channel Myasthenia Reveal That a Valine Ring in the Channel Pore of Muscle AChR is Optimized for Stabilizing Channel Gating. 27375219 2016
Entrez Id: 1140
Gene Symbol: CHRNB1
CHRNB1 		0.600 GeneticVariation disease CLINVAR Molecular characterisation of congenital myasthenic syndromes in Southern Brazil. 20562457 2010
Entrez Id: 1140
Gene Symbol: CHRNB1
CHRNB1 		0.600 GeneticVariation disease CLINVAR New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome. 8872460 1996
Entrez Id: 1140
Gene Symbol: CHRNB1
CHRNB1 		0.600 GeneticVariation disease UNIPROT A beta-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndrome. 8651643 1996
Entrez Id: 1140
Gene Symbol: CHRNB1
CHRNB1 		0.600 GeneticVariation disease UNIPROT New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome. 8872460 1996
Entrez Id: 1140
Gene Symbol: CHRNB1
CHRNB1 		0.600 Biomarker disease GENOMICS_ENGLAND The effect of polyamine on the casein phosphorylation by protein kinase isolated from rat liver nucle-. 616314 1977
Entrez Id: 1140
Gene Symbol: CHRNB1
CHRNB1 		0.600 CausalMutation disease CLINVAR