abnormal heart left ventricle pressure Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the pressure within the left cardiac ventricle (Mammalian Phenotype Ontology, MP_0010754)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010754
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32 gene mutations causing the abnormal heart left ventricle pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCY6 adenylate cyclase 6
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
BBC3 BCL2 binding component 3
CNOT3 CCR4-NOT transcription complex, subunit 3
DNM1L dynamin 1-like
EGFR epidermal growth factor receptor
FGF2 fibroblast growth factor 2 (basic)
FSTL3 follistatin-like 3 (secreted glycoprotein)
HSPB8 heat shock 22kDa protein 8
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LEPR leptin receptor
MAOA monoamine oxidase A
MUS81 MUS81 structure-specific endonuclease subunit
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
MYLK3 myosin light chain kinase 3
NDUFS6 NADH dehydrogenase (ubiquinone) Fe-S protein 6, 13kDa (NADH-coenzyme Q reductase)
NOS2 nitric oxide synthase 2, inducible
NOS3 nitric oxide synthase 3 (endothelial cell)
NRG1 neuregulin 1
PDLIM5 PDZ and LIM domain 5
PLN phospholamban
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1
TERC telomerase RNA component
TIMP1 TIMP metallopeptidase inhibitor 1
TIMP3 TIMP metallopeptidase inhibitor 3
TNNT2 troponin T type 2 (cardiac)
TPH1 tryptophan hydroxylase 1
TRPV1 transient receptor potential cation channel, subfamily V, member 1
TTN titin
VEGFA vascular endothelial growth factor A
WRN Werner syndrome, RecQ helicase-like