split sternal manubrium Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the appearance of an abnormal division of the cranial most segment of the sternum (Mammalian Phenotype Ontology, MP_0012667)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012667
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3 gene mutations causing the split sternal manubrium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGFR2 fibroblast growth factor receptor 2
GLI3 GLI family zinc finger 3
MKS1 Meckel syndrome, type 1