decreased maxillary shelf size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the bony projection of the maxilla that normally fuses with palatine shelf to form secondary (hard) palate (Mammalian Phenotype Ontology, MP_0009897)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009897
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Genes

7 gene mutations causing the decreased maxillary shelf size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDON cell adhesion associated, oncogene regulated
DLX5 distal-less homeobox 5
EDNRB endothelin receptor type B
EYA1 EYA transcriptional coactivator and phosphatase 1
MN1 meningioma (disrupted in balanced translocation) 1
PRRX1 paired related homeobox 1
RSPO2 R-spondin 2