abnormal parturition Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description defect in the process of labor and delivery in female animals (Mammalian Phenotype Ontology, MP_0002907)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002907
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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)