temporal bone hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, in the large, irregular bone located at the base and side of the skull (Mammalian Phenotype Ontology, MP_0004424)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004424
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2 gene mutations causing the temporal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MN1 meningioma (disrupted in balanced translocation) 1
TCOF1 Treacher Collins-Franceschetti syndrome 1