absent squamosal bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the thin, plate-like part of the temporal bone (Mammalian Phenotype Ontology, MP_0004899)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004899
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4 gene mutations causing the absent squamosal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHRD chordin
MN1 meningioma (disrupted in balanced translocation) 1
POU3F3 POU class 3 homeobox 3
PRRX1 paired related homeobox 1