absent allantois Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing fetal membrane which contributes to the formation of the umbilical cord and placenta (Mammalian Phenotype Ontology, MP_0003087)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003087
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Genes

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

Symbol Name
ACVR1 activin A receptor, type I
BMP4 bone morphogenetic protein 4
BMP8B bone morphogenetic protein 8b
CTDNEP1 CTD nuclear envelope phosphatase 1
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CUBN cubilin (intrinsic factor-cobalamin receptor)
DAB2 Dab, mitogen-responsive phosphoprotein, homolog 2 (Drosophila)
GNPNAT1 glucosamine-phosphate N-acetyltransferase 1
HNF4A hepatocyte nuclear factor 4, alpha
LDB1 LIM domain binding 1
LIN9 lin-9 DREAM MuvB core complex component
MLLT4 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 4
NODAL nodal growth differentiation factor
PRKCI protein kinase C, iota
SLC31A1 solute carrier family 31 (copper transporter), member 1
SMAD2 SMAD family member 2
T T, brachyury homolog (mouse)
TFAP2C transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma)
WNT3 wingless-type MMTV integration site family, member 3