absent amnion Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	absence of the thin innermost layer of the extraembryonic membranes that contains the amniotic fluid; the membrane forms a closed sac in which the embryo and later, the fetus, is suspended and protected (Mammalian Phenotype Ontology, MP_0005030)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005030
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Genes

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

Symbol	Name
ACVR1	activin A receptor, type I
AMN	amnion associated transmembrane protein
CTDNEP1	CTD nuclear envelope phosphatase 1
CUBN	cubilin (intrinsic factor-cobalamin receptor)
CUL3	cullin 3
DAB2	Dab, mitogen-responsive phosphoprotein, homolog 2 (Drosophila)
DHX9	DEAH (Asp-Glu-Ala-His) box helicase 9
GNPNAT1	glucosamine-phosphate N-acetyltransferase 1
HNF4A	hepatocyte nuclear factor 4, alpha
HSP90B1	heat shock protein 90kDa beta (Grp94), member 1
LIN9	lin-9 DREAM MuvB core complex component
NODAL	nodal growth differentiation factor
PALB2	partner and localizer of BRCA2
PAXIP1	PAX interacting (with transcription-activation domain) protein 1
SMAD2	SMAD family member 2
SNAI1	snail family zinc finger 1
WNT3	wingless-type MMTV integration site family, member 3