abnormal umbilical cord blood vessel morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the three blood vessels, usually one large umbilical vein and two small umbilical arteries, buried within Wharton's jelly, that transport blood to and from the placenta, where exchange between the mother and fetus takes place; the umbilical vein carries oxygenated, nutrient-rich blood from the placenta to the fetus, and the umbilical arteries carry deoxygenated, nutrient-depleted blood from the fetus to the placenta (Mammalian Phenotype Ontology, MP_0012300)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012300
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Genes

8 gene mutations causing the abnormal umbilical cord blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADM adrenomedullin
BMP5 bone morphogenetic protein 5
CDH5 cadherin 5, type 2 (vascular endothelium)
DLL4 delta-like 4 (Drosophila)
HOXA13 homeobox A13
PAM peptidylglycine alpha-amidating monooxygenase
RAMP2 receptor (G protein-coupled) activity modifying protein 2
TBX4 T-box 4