absent maxillary shelf Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing bony projection of the maxilla that normally fuses with palatine shelf to form secondary (hard) palate (Mammalian Phenotype Ontology, MP_0000430)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000430
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9 gene mutations causing the absent maxillary shelf phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDON cell adhesion associated, oncogene regulated
DLX2 distal-less homeobox 2
GLI2 GLI family zinc finger 2
HAND2 heart and neural crest derivatives expressed 2
JAG2 jagged 2
MSX1 msh homeobox 1
PAX9 paired box 9
PRRX1 paired related homeobox 1
TGFB2 transforming growth factor, beta 2