Details
| Type | Protein Coding |
| Official Symbol | CHRNB1 |
| Official Name | cholinergic receptor nicotinic beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:1961] |
| Ensembl ID | ENSG00000283946 |
| Bio databases IDs | |
| Aliases | cholinergic receptor nicotinic beta 1 subunit |
| Species | Human, Homo sapiens |
Pathways
Biological processes and signaling networks where the CHRNB1 gene in human plays a role, providing insight into its function and relevance in health or disease.
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- MYASTHENIC SYNDROME CONGENITAL 2A SLOW-CHANNEL
- MYASTHENIC SYNDROME CONGENITAL 2C ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY