Symbol Name ID |
Myh7
myosin, heavy polypeptide 7, cardiac muscle, beta MGI:2155600 |
Darker colors indicate more annotations |
Human Phenotypes | Pulmonary artery hypoplasia |
Pulmonary arterial hypertension |
Exertional dyspnea |
Reduced vital capacity |
Restrictive ventilatory defect |
Respiratory insufficiency |
Disease(s) Associated with MYH7 | ||||||
autosomal dominant hyaline body myopathy | ||||||
autosomal recessive hyaline body myopathy | ||||||
dilated cardiomyopathy 1S |
Mouse Phenotypes | increased lung weight |
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Availability | Mouse Genotype | |
Tg(Myh6-Myh7)102Rbns/Tg(Myh6-Myh7)102Rbns | ||
Tg(Myh6-Myh7)137Rbns/0 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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