abnormal gestational length Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the usual duration of time between when a fertilized egg implants in the wall of the uterus and the birth of offspring (Mammalian Phenotype Ontology, MP_0002292)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002292
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12 gene mutations causing the abnormal gestational length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AKR1C3 aldo-keto reductase family 1, member C3
ALPPL2 alkaline phosphatase, placental-like 2
B4GALT1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1
BMP2 bone morphogenetic protein 2
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CENPB centromere protein B, 80kDa
COMT catechol-O-methyltransferase
FSHR follicle stimulating hormone receptor
GHR growth hormone receptor
INHBB inhibin, beta B
LPAR3 lysophosphatidic acid receptor 3
TIPARP TCDD-inducible poly(ADP-ribose) polymerase