absent premaxilla Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing anterior and interior portion of the maxilla (Mammalian Phenotype Ontology, MP_0000090)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000090
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2 gene mutations causing the absent premaxilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EYA1 EYA transcriptional coactivator and phosphatase 1
MSX1 msh homeobox 1