thick ventricular wall Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased depth of the cardiac wall of the heart ventricles (Mammalian Phenotype Ontology, MP_0002953)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002953
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Genes

31 gene mutations causing the thick ventricular wall phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABL1 ABL proto-oncogene 1, non-receptor tyrosine kinase
ADAM17 ADAM metallopeptidase domain 17
ADM adrenomedullin
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
BIN1 bridging integrator 1
CASQ2 calsequestrin 2 (cardiac muscle)
CAV1 caveolin 1, caveolae protein, 22kDa
CAV3 caveolin 3
EPAS1 endothelial PAS domain protein 1
EPO erythropoietin
EPOR erythropoietin receptor
FKBP1B FK506 binding protein 1B, 12.6 kDa
HDAC2 histone deacetylase 2
HOPX HOP homeobox
IDUA iduronidase, alpha-L-
IGF2R insulin-like growth factor 2 receptor
LBX1 ladybird homeobox 1
MMP9 matrix metallopeptidase 9
MYBPC3 myosin binding protein C, cardiac
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
PDGFA platelet-derived growth factor alpha polypeptide
PEPD peptidase D
PNMT phenylethanolamine N-methyltransferase
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RYR2 ryanodine receptor 2 (cardiac)
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4
SMTN smoothelin
TNNI3 troponin I type 3 (cardiac)
TRIP11 thyroid hormone receptor interactor 11