pregnancy-related premature death Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description death occurring before the normal life span of an organism, occurring during pregnancy, parturition or lactation (Mammalian Phenotype Ontology, MP_0008028)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008028
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Genes

18 gene mutations causing the pregnancy-related premature death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM19 ADAM metallopeptidase domain 19
ANTXR2 anthrax toxin receptor 2
AP3B1 adaptor-related protein complex 3, beta 1 subunit
B3GNT5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5
CENPB centromere protein B, 80kDa
DERL2 derlin 2
F13A1 coagulation factor XIII, A1 polypeptide
F3 coagulation factor III (thromboplastin, tissue factor)
INHBB inhibin, beta B
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
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
PFDN5 prefoldin subunit 5
PPP1R13L protein phosphatase 1, regulatory subunit 13 like