Gene table: search width pubmed_id = 2144212


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

protein
All allelic disease phenotypes - locus/disease symbols
Familial hypertrophic cardiomyopathy, 1 - (AD)
10.1
1975475
2144212
2811944
MYH6 (14q12)
Myosin heavy chain 6
MYH7 (14q12)
Myosin, heavy polypeptide 7, cardiac muscle, beta
* Cardiomyopathy, dilated, 1EE - CMD1EE
* Familial hypertrophic cardiomyopathy, 14 - CMH14
* Sick sinus syndrome 3 - SSS3
* Cardiomyopathy, familial hypertrophic 1 - CMH1
* Cardiomyopathy, dilated, 1S - CMD1S
* myopathy, congenital, with fiber-type disproportion - CFTD
* Myopathy, distal 1 - MPD1
* cardiomyopathy, familial hypertrophic, 1, included - CMH1
* Left ventricular noncompaction 5 - LVNC5
* Myosin storage myopathy