abnormal fetal cardiomyocyte morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of fetal and neonatal heart cells that undergo proliferation and are not yet terminally differentiated into binucleate or multinucleate cardiac myocytes (Mammalian Phenotype Ontology, MP_0008788)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008788
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Genes

20 gene mutations causing the abnormal fetal cardiomyocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRG6 adhesion G protein-coupled receptor G6
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
DAAM1 dishevelled associated activator of morphogenesis 1
FOXM1 forkhead box M1
GATA5 GATA binding protein 5
HEXIM1 hexamethylene bis-acetamide inducible 1
HSP90B1 heat shock protein 90kDa beta (Grp94), member 1
MAPK14 mitogen-activated protein kinase 14
MB myoglobin
MYH10 myosin, heavy chain 10, non-muscle
NCOA6 nuclear receptor coactivator 6
PARVA parvin, alpha
PEPD peptidase D
PIP5K1C phosphatidylinositol-4-phosphate 5-kinase, type I, gamma
PPARG peroxisome proliferator-activated receptor gamma
RYR2 ryanodine receptor 2 (cardiac)
SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1
SPEG SPEG complex locus
TH tyrosine hydroxylase
TSC1 tuberous sclerosis 1