abnormal umbilical cord morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the connective stalk between the fetus and the placenta (Mammalian Phenotype Ontology, MP_0001725)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001725
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23 gene mutations causing the abnormal umbilical cord morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM10 ADAM metallopeptidase domain 10
ADM adrenomedullin
BMP5 bone morphogenetic protein 5
CDH5 cadherin 5, type 2 (vascular endothelium)
COL27A1 collagen, type XXVII, alpha 1
DLL4 delta-like 4 (Drosophila)
ERF Ets2 repressor factor
F9 coagulation factor IX
FGFR2 fibroblast growth factor receptor 2
GAD1 glutamate decarboxylase 1 (brain, 67kDa)
GPC3 glypican 3
HOXA13 homeobox A13
IFT27 intraflagellar transport 27
LRP2 low density lipoprotein receptor-related protein 2
NBEA neurobeachin
NPRL3 nitrogen permease regulator-like 3 (S. cerevisiae)
PAM peptidylglycine alpha-amidating monooxygenase
RAMP2 receptor (G protein-coupled) activity modifying protein 2
SLC32A1 solute carrier family 32 (GABA vesicular transporter), member 1
SMAD1 SMAD family member 1
TBX4 T-box 4
TP63 tumor protein p63
VANGL2 VANGL planar cell polarity protein 2