cardiomyopathies Gene Set
| Dataset |
GAD Gene-Disease Associations
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| Category |
disease or phenotype associations
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| Type |
disease |
| Description |
A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. (Human Disease Ontology, DOID_0050700)
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| Similar Terms |
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| Downloads & Tools |
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Genes
10 genes associated with the disease cardiomyopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACE
|
angiotensin I converting enzyme
|
|
ACTC1
|
actin, alpha, cardiac muscle 1
|
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HLA-DRB1
|
major histocompatibility complex, class II, DR beta 1
|
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KNG1
|
kininogen 1
|
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MYBPC3
|
myosin binding protein C, cardiac
|
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MYH7
|
myosin, heavy chain 7, cardiac muscle, beta
|
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PLAT
|
plasminogen activator, tissue
|
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SLC22A5
|
solute carrier family 22 (organic cation/carnitine transporter), member 5
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TNF
|
tumor necrosis factor
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TNNT2
|
troponin T type 2 (cardiac)
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