absent palatine bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of either of two irregularly L-shaped bones located posterior to the maxilla that in part forms the back of the hard palate, part of the nasal cavity and part of the floor of the orbits (Mammalian Phenotype Ontology, MP_0004476)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004476
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Genes

2 gene mutations causing the absent palatine bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXC2 forkhead box C2
MNT MAX network transcriptional repressor