Gene table: search width pubmed_id = 20303757


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
Cap myopathy - (AD)
3.43
20303757
ACTA1 (1q42.1)
Alpha actin, skeletal muscle
* myopathy, congenital, with fiber-type disproportion - CFTD
* Congenital muscular dystrophy with rigid spine related to ACTA1
* Left ventricular noncompaction 4 - LVNC4
* Nemaline myopathy 3 - NEM3