Gene table: search width pubmed_id = 12651869


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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, 11, associated with acetylcholine receptor deficiency - (AR)
11.19
11791205
12651869
RAPSN (11p11.2-p11.1)
Rapsyn
* Myasthenic syndrome, congenital - CMS1D
* Fetal akinesia deformation sequence 2 - FADS2
* Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency - CMS11