abnormal coronary artery morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of any of the arteries that branch from the ascending aorta to supply blood to the heart (Mammalian Phenotype Ontology, MP_0004111)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004111
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Genes

26 gene mutations causing the abnormal coronary artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADM adrenomedullin
AHR aryl hydrocarbon receptor
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
DYX1C1 dyslexia susceptibility 1 candidate 1
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
FAS Fas cell surface death receptor
GJA1 gap junction protein, alpha 1, 43kDa
GPC3 glypican 3
HECTD1 HECT domain containing E3 ubiquitin protein ligase 1
HEXIM1 hexamethylene bis-acetamide inducible 1
HSPG2 heparan sulfate proteoglycan 2
LTBP1 latent transforming growth factor beta binding protein 1
MEGF8 multiple EGF-like-domains 8
NRP1 neuropilin 1
PDPN podoplanin
PLXND1 plexin D1
RRM2B ribonucleotide reductase M2 B (TP53 inducible)
RYR1 ryanodine receptor 1 (skeletal)
SGCD sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
SOX4 SRY (sex determining region Y)-box 4
SUFU suppressor of fused homolog (Drosophila)
TDG thymine-DNA glycosylase
TGFBR1 transforming growth factor, beta receptor 1
TGFBR2 transforming growth factor, beta receptor II (70/80kDa)
VEGFA vascular endothelial growth factor A