basisphenoid bone foramen Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the presence of one or more holes in part of the base of the cranium between the basioccipital and the presphenoid, which usually ossifies separately in the embryo or in the young, and becomes a part of the sphenoid in the adult; in many animals it persists as a separate bone between the basioccipital bone and the presphenoidal bone (Mammalian Phenotype Ontology, MP_0004463)
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7 gene mutations causing the basisphenoid bone foramen phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP7 bone morphogenetic protein 7
BMPER BMP binding endothelial regulator
CDON cell adhesion associated, oncogene regulated
GLI3 GLI family zinc finger 3
OTX2 orthodenticle homeobox 2
PKDCC protein kinase domain containing, cytoplasmic
TMEM107 transmembrane protein 107