absent allantois Gene Set
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
|
