absent frontal bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the bone forming the forehead and roof of the eye orbit (Mammalian Phenotype Ontology, MP_0004376)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004376
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5 gene mutations causing the absent frontal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GTF2IRD1 GTF2I repeat domain containing 1
HSPG2 heparan sulfate proteoglycan 2
SKI SKI proto-oncogene
TCOF1 Treacher Collins-Franceschetti syndrome 1
WDR19 WD repeat domain 19