abnormal orbitosphenoid bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the bone that is situated in the orbit on either side of the presphenoid; it generally forms a part of the sphenoid in the adult, and may be independent in the young (Mammalian Phenotype Ontology, MP_0004457)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004457
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5 gene mutations causing the abnormal orbitosphenoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GLI3 GLI family zinc finger 3
OTX1 orthodenticle homeobox 1
OTX2 orthodenticle homeobox 2
RARB retinoic acid receptor, beta
RARG retinoic acid receptor, gamma