abnormal cardiac output Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the blood volume pumped by each ventricle per minute (stroke volume x heart rate) (Mammalian Phenotype Ontology, MP_0001627)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001627
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Genes

23 gene mutations causing the abnormal cardiac output phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
ARSB arylsulfatase B
DDAH1 dimethylarginine dimethylaminohydrolase 1
ELN elastin
GIPC1 GIPC PDZ domain containing family, member 1
GJC1 gap junction protein, gamma 1, 45kDa
IDUA iduronidase, alpha-L-
KLF3 Kruppel-like factor 3 (basic)
KLK3 kallikrein-related peptidase 3
LEPR leptin receptor
MAPK1 mitogen-activated protein kinase 1
MLYCD malonyl-CoA decarboxylase
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
NPPA natriuretic peptide A
NRG1 neuregulin 1
PDCD1 programmed cell death 1
PDLIM3 PDZ and LIM domain 3
PPARGC1A peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
PRKG1 protein kinase, cGMP-dependent, type I
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RXRA retinoid X receptor, alpha
TMOD1 tropomodulin 1
TPH1 tryptophan hydroxylase 1