Gene table: search width pubmed_id = 25192047


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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, 7, presynaptic and distal motor neuropathy, autosomal dominant - (AD)
11.14
25192047
SYT2 (1q32.1)
Synaptotagmin II
* Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy - MYSPC
* Distal motor neuropathy related to SYT2
* Myasthenic syndrome, congenital, 7B, presynaptic - CMS7B
* Myasthenic syndrome, congenital, 7, presynaptic and distal motor neuropathy, autosomal dominant - CMS7A