Gene table: search width pubmed_id = 24610330


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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, 22
11.30
24610330
PREPL (2p21)
Prolyl endopeptidase-like
* Myasthenic syndrome, congenital, 22 - CMS22