abnormal placenta physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the organ of metabolic interchange between fetus and mother, which is partly of embryonic origin and partly of maternal origin (Mammalian Phenotype Ontology, MP_0010038)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010038
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22 gene mutations causing the abnormal placenta physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADM adrenomedullin
CDH1 cadherin 1, type 1, E-cadherin (epithelial)
CHORDC1 cysteine and histidine-rich domain (CHORD) containing 1
COPS5 COP9 signalosome subunit 5
ERN1 endoplasmic reticulum to nucleus signaling 1
GJB2 gap junction protein, beta 2, 26kDa
HAND1 heart and neural crest derivatives expressed 1
HEPH hephaestin
IGF2 insulin-like growth factor 2
KRT8 keratin 8, type II
MAPK14 mitogen-activated protein kinase 14
MECP2 methyl CpG binding protein 2
MED1 mediator complex subunit 1
NCOA6 nuclear receptor coactivator 6
PNPLA6 patatin-like phospholipase domain containing 6
RB1 retinoblastoma 1
RTL1 retrotransposon-like 1
SLC2A3 solute carrier family 2 (facilitated glucose transporter), member 3
SPINT1 serine peptidase inhibitor, Kunitz type 1
SSR3 signal sequence receptor, gamma (translocon-associated protein gamma)
STIP1 stress-induced phosphoprotein 1
TADA3 transcriptional adaptor 3