absent palatine bone horizontal plate Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing bony plate of the palatine bone that normally fuses with maxillary shelf to form secondary (hard) palate (Mammalian Phenotype Ontology, MP_0000431)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000431
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9 gene mutations causing the absent palatine bone horizontal plate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CYP51A1 cytochrome P450, family 51, subfamily A, polypeptide 1
DLX2 distal-less homeobox 2
DLX5 distal-less homeobox 5
EDNRB endothelin receptor type B
GLI2 GLI family zinc finger 2
JAG2 jagged 2
MSX1 msh homeobox 1
PAX9 paired box 9
PRRX1 paired related homeobox 1