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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Genes

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