absent myocardial trabeculae Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the supporting bundles of muscular fibers lining the walls of the heart (Mammalian Phenotype Ontology, MP_0000293)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000293
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22 gene mutations causing the absent myocardial trabeculae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
ANGPT1 angiopoietin 1
ARID1A AT rich interactive domain 1A (SWI-like)
EFNB2 ephrin-B2
EP300 E1A binding protein p300
EPHB4 EPH receptor B4
ERBB2 erb-b2 receptor tyrosine kinase 2
ERBB4 erb-b2 receptor tyrosine kinase 4
GJC1 gap junction protein, gamma 1, 45kDa
HAND2 heart and neural crest derivatives expressed 2
HAS2 hyaluronan synthase 2
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
HTR2B 5-hydroxytryptamine (serotonin) receptor 2B, G protein-coupled
MAPK14 mitogen-activated protein kinase 14
NKX2-5 NK2 homeobox 5
NR2F2 nuclear receptor subfamily 2, group F, member 2
NRG1 neuregulin 1
OVOL2 ovo-like zinc finger 2
POR P450 (cytochrome) oxidoreductase
TEK TEK tyrosine kinase, endothelial
TMOD1 tropomodulin 1
XBP1 X-box binding protein 1