abnormal fetal ductus arteriosus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the fetal vessel that connects the left pulmonary artery with the descending aorta; the ductus arteriosus normally regresses into a fibrous cord, the ligamentum arteriousum after birth (Mammalian Phenotype Ontology, MP_0010564)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010564
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Genes

16 gene mutations causing the abnormal fetal ductus arteriosus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
EDNRA endothelin receptor type A
FOXC1 forkhead box C1
GPC3 glypican 3
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD)
NTF3 neurotrophin 3
PCSK5 proprotein convertase subtilisin/kexin type 5
PLXND1 plexin D1
PRRX1 paired related homeobox 1
PTGER4 prostaglandin E receptor 4 (subtype EP4)
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
RIPPLY3 ripply transcriptional repressor 3
SLCO2A1 solute carrier organic anion transporter family, member 2A1
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
TBC1D32 TBC1 domain family, member 32
TFAP2B transcription factor AP-2 beta (activating enhancer binding protein 2 beta)