myocardial necrosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006085
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Genes

20 gene mutations causing the myocardial necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DES desmin
DMD dystrophin
HMOX1 heme oxygenase 1
IGHMBP2 immunoglobulin mu binding protein 2
LMNA lamin A/C
MED30 mediator complex subunit 30
MKL1 megakaryoblastic leukemia (translocation) 1
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
NPR1 natriuretic peptide receptor 1
PPARA peroxisome proliferator-activated receptor alpha
PPP1R13L protein phosphatase 1, regulatory subunit 13 like
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
SGCD sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4
SOD1 superoxide dismutase 1, soluble
SOD2 superoxide dismutase 2, mitochondrial
SPTA1 spectrin, alpha, erythrocytic 1
TGFB1 transforming growth factor, beta 1
XBP1 X-box binding protein 1