Gene table: search width pubmed_id = 28017374


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
Nemaline myopathy 11 - (AE)
3.14
28017374
28220527
MYPN (10q21.1)
Myopalladin
* Hypertrophic cardiomyopathy related to cardiac myopalladin - CMH22
* Nemaline myopathy - NEM11