Gene table: search width pubmed_id = 8872460


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Myasthenic syndrome, congenital, 1A, Slow-channel - (AD)
11.1
7619526
8872460
9158151
CHRNA1 (2q24-q32)
Cholinergic receptor, nicotinic, alpha polypeptide 1
* Myasthenic syndrome, fast-channel congenital - FCCMS
* Myasthenic syndrome, slow-channel congenital - SCCMS
* Myasthenic syndrome, congenital associated with acetylcholine receptor deficiency
* Myasthenic syndrome, congenital, 1B, Fast-channel - CMS1B
* Myasthenic syndrome, congenital, 1A, Slow-channel - CMS1A