Gene table: search width pubmed_id = 17372140


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Myopathy, myosin storage, autosomal dominant (eccentric core disease) - (AR)
3.51
17372140
MYH7 (14q12)
Myosin, heavy polypeptide 7, cardiac muscle, beta
* Cardiomyopathy, dilated, 1S - CMD1S
* Myopathy, distal 1 - MPD1
* cardiomyopathy, familial hypertrophic, 1, included - CMH1
* Congenital myopathy 7B, myosin storage, autosomal recessive - CMYP7B
* Congenital myopathy 7A, myosin storage, autosomal dominant - CMYP7A
* Left ventricular noncompaction 5 - LVNC5
* Myopathy, myosin storage, autosomal dominant - MSMB
* Myosin storage myopathy