frontal bone foramen Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description presence of a hole in the bone forming the forehead and roof of the eye orbit (Mammalian Phenotype Ontology, MP_0004378)
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3 gene mutations causing the frontal bone foramen phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EFNB1 ephrin-B1
HDAC8 histone deacetylase 8
MSX2 msh homeobox 2