abnormal cardiac muscle relaxation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description altered ability of the cardiac/heart muscle to lengthen following contractions, often measured by dP/dt min (Mammalian Phenotype Ontology, MP_0004084)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004084
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21 gene mutations causing the abnormal cardiac muscle relaxation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
DES desmin
DNM1L dynamin 1-like
FGF2 fibroblast growth factor 2 (basic)
GLRX3 glutaredoxin 3
HPRT1 hypoxanthine phosphoribosyltransferase 1
IDUA iduronidase, alpha-L-
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
MYBPC3 myosin binding protein C, cardiac
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
NDUFS6 NADH dehydrogenase (ubiquinone) Fe-S protein 6, 13kDa (NADH-coenzyme Q reductase)
NOS1 nitric oxide synthase 1 (neuronal)
NOS3 nitric oxide synthase 3 (endothelial cell)
PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
PLN phospholamban
PRKG1 protein kinase, cGMP-dependent, type I
SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1
SRL sarcalumenin
TERC telomerase RNA component
TIMP3 TIMP metallopeptidase inhibitor 3
VEGFA vascular endothelial growth factor A