Gene table: search width pubmed_id = 8205619


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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, 3 - (AD)
10.3
8205619
TPM1 (15q22)
Tropomyosin 1 (alpha)
* Cardiomyopathy, dilated, 1Y - CMD1Y
* Left ventricular noncompaction 9 - LVNC9
* Cardiomyopathy, familial hypertrophic, 3 - CMH3