absent chorion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the outermost extraembryonic membrane (Mammalian Phenotype Ontology, MP_0009593)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009593
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Genes

14 gene mutations causing the absent chorion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR1 activin A receptor, type I
BPTF bromodomain PHD finger transcription factor
CUBN cubilin (intrinsic factor-cobalamin receptor)
DAB2 Dab, mitogen-responsive phosphoprotein, homolog 2 (Drosophila)
ELF5 E74-like factor 5 (ets domain transcription factor)
ESRRB estrogen-related receptor beta
GNPNAT1 glucosamine-phosphate N-acetyltransferase 1
HNF4A hepatocyte nuclear factor 4, alpha
HSD17B12 hydroxysteroid (17-beta) dehydrogenase 12
HSP90B1 heat shock protein 90kDa beta (Grp94), member 1
LIN9 lin-9 DREAM MuvB core complex component
SMAD2 SMAD family member 2
SNAI1 snail family zinc finger 1
WNT3 wingless-type MMTV integration site family, member 3