abnormal maternal decidual layer morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the maternal uterine-derived portion of the placenta (Mammalian Phenotype Ontology, MP_0004256)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004256
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Genes

21 gene mutations causing the abnormal maternal decidual layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADM adrenomedullin
AKT1 v-akt murine thymoma viral oncogene homolog 1
CALCRL calcitonin receptor-like
CBS cystathionine-beta-synthase
COMT catechol-O-methyltransferase
CR1L complement component (3b/4b) receptor 1-like
EGFR epidermal growth factor receptor
ELAVL1 ELAV like RNA binding protein 1
FBN1 fibrillin 1
HCST hematopoietic cell signal transducer
IFNG interferon, gamma
IFNGR1 interferon gamma receptor 1
IL11RA interleukin 11 receptor, alpha
IL15 interleukin 15
IL2RG interleukin 2 receptor, gamma
ITGB7 integrin, beta 7
LIF leukemia inhibitory factor
PTP4A2 protein tyrosine phosphatase type IVA, member 2
SMCHD1 structural maintenance of chromosomes flexible hinge domain containing 1
TYROBP TYRO protein tyrosine kinase binding protein
WNT6 wingless-type MMTV integration site family, member 6