Gene table: search width pubmed_id = 22286171


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
Restrictive cardiomyopathy, 4 - (AD)
10.88
22286171
MYPN (10q21.1)
Myopalladin
* Hypertrophic cardiomyopathy related to cardiac myopalladin - CMH22
* Nemaline myopathy - NEM11