abnormal extraembryonic tissue physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the membranes involved with embryonic protection and nutrition (Mammalian Phenotype Ontology, MP_0004264)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004264
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34 gene mutations causing the abnormal extraembryonic tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADM adrenomedullin
ARC activity-regulated cytoskeleton-associated protein
CDC73 cell division cycle 73
CDH1 cadherin 1, type 1, E-cadherin (epithelial)
CDX2 caudal type homeobox 2
CHORDC1 cysteine and histidine-rich domain (CHORD) containing 1
COPS5 COP9 signalosome subunit 5
ERN1 endoplasmic reticulum to nucleus signaling 1
FBXL5 F-box and leucine-rich repeat protein 5
GJB2 gap junction protein, beta 2, 26kDa
HAND1 heart and neural crest derivatives expressed 1
HEPH hephaestin
IGF2 insulin-like growth factor 2
KAT8 K(lysine) acetyltransferase 8
KLF5 Kruppel-like factor 5 (intestinal)
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
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RB1 retinoblastoma 1
RTL1 retrotransposon-like 1
SLC2A3 solute carrier family 2 (facilitated glucose transporter), member 3
SMARCA5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
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
XBP1 X-box binding protein 1
ZNF24 zinc finger protein 24
ZNF830 zinc finger protein 830