abnormal heart left ventricle weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the average weight of the left ventricle compared to the control (Mammalian Phenotype Ontology, MP_0020204)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0020204
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Genes

21 gene mutations causing the abnormal heart left ventricle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTR2 angiotensin II receptor, type 2
CKM creatine kinase, muscle
COX7A1 cytochrome c oxidase subunit VIIa polypeptide 1 (muscle)
CSRP3 cysteine and glycine-rich protein 3 (cardiac LIM protein)
EPO erythropoietin
GATA5 GATA binding protein 5
IDUA iduronidase, alpha-L-
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
MYLK3 myosin light chain kinase 3
NCOR1 nuclear receptor corepressor 1
NDUFS6 NADH dehydrogenase (ubiquinone) Fe-S protein 6, 13kDa (NADH-coenzyme Q reductase)
NEDD4L neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase
PLA2G4A phospholipase A2, group IVA (cytosolic, calcium-dependent)
PNPLA2 patatin-like phospholipase domain containing 2
SMTN smoothelin
TERC telomerase RNA component
THBS4 thrombospondin 4
TIMP4 TIMP metallopeptidase inhibitor 4
TLR2 toll-like receptor 2
TTN titin
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor