abnormal parturition Gene Set
Genes
22 gene mutations causing the abnormal parturition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Symbol |
Name |
AKR1C3
|
aldo-keto reductase family 1, member C3
|
ANTXR2
|
anthrax toxin receptor 2
|
B4GALT1
|
UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1
|
CENPB
|
centromere protein B, 80kDa
|
CLOCK
|
clock circadian regulator
|
CNR1
|
cannabinoid receptor 1 (brain)
|
DLL3
|
delta-like 3 (Drosophila)
|
DSCAM
|
Down syndrome cell adhesion molecule
|
GADD45A
|
growth arrest and DNA-damage-inducible, alpha
|
HPGD
|
hydroxyprostaglandin dehydrogenase 15-(NAD)
|
KALRN
|
kalirin, RhoGEF kinase
|
KCNN3
|
potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 3
|
KPNA1
|
karyopherin alpha 1 (importin alpha 5)
|
NR1H2
|
nuclear receptor subfamily 1, group H, member 2
|
NRK
|
Nik related kinase
|
OXT
|
oxytocin/neurophysin I prepropeptide
|
PLA2G4A
|
phospholipase A2, group IVA (cytosolic, calcium-dependent)
|
PTGFR
|
prostaglandin F receptor (FP)
|
PTGS1
|
prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
|
RLN1
|
relaxin 1
|
RXFP1
|
relaxin/insulin-like family peptide receptor 1
|
SRD5A1
|
steroid-5-alpha-reductase, alpha polypeptide 1 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 1)
|