Gene table: search width pubmed_id = 27590285


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Myasthenic syndrome, congenital, 21 - (AR)
11.27
27590285
SLC18A3 (10q11.2)
Solute Carrier Family 18 (Vesicular Acetylcholine), Member 3
* Myasthenic Syndrome, Congenital, 21, Presynaptic - CMS21