abnormal maxillary shelf morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the bony projection of the maxilla that normally fuses with palatine shelf to form secondary (hard) palate (Mammalian Phenotype Ontology, MP_0004538)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004538
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Genes

20 gene mutations causing the abnormal maxillary shelf morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP7 bone morphogenetic protein 7
BNC2 basonuclin 2
CDON cell adhesion associated, oncogene regulated
DLX2 distal-less homeobox 2
DLX5 distal-less homeobox 5
EDNRB endothelin receptor type B
EYA1 EYA transcriptional coactivator and phosphatase 1
FOXF2 forkhead box F2
GLG1 golgi glycoprotein 1
GLI2 GLI family zinc finger 2
HAND2 heart and neural crest derivatives expressed 2
JAG2 jagged 2
MN1 meningioma (disrupted in balanced translocation) 1
MSX1 msh homeobox 1
PAX6 paired box 6
PAX9 paired box 9
PRRX1 paired related homeobox 1
RSPO2 R-spondin 2
TGFB2 transforming growth factor, beta 2
ZEB1 zinc finger E-box binding homeobox 1