abnormal palatine bone horizontal plate morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the bony plate of the palatine bone that normally fuses with maxillary shelf to form secondary (hard) palate (Mammalian Phenotype Ontology, MP_0004537)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004537
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Genes

25 gene mutations causing the abnormal palatine bone horizontal plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARID5B AT rich interactive domain 5B (MRF1-like)
CSRNP1 cysteine-serine-rich nuclear protein 1
CYP51A1 cytochrome P450, family 51, subfamily A, polypeptide 1
DLX2 distal-less homeobox 2
DLX5 distal-less homeobox 5
EDNRB endothelin receptor type B
EYA1 EYA transcriptional coactivator and phosphatase 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FOXC2 forkhead box C2
FOXF2 forkhead box F2
GLI2 GLI family zinc finger 2
GLI3 GLI family zinc finger 3
IRF6 interferon regulatory factor 6
JAG2 jagged 2
MN1 meningioma (disrupted in balanced translocation) 1
MSX1 msh homeobox 1
PAX9 paired box 9
PRRX1 paired related homeobox 1
RSPO2 R-spondin 2
SCHIP1 schwannomin interacting protein 1
SGPL1 sphingosine-1-phosphate lyase 1
TBX22 T-box 22
TIPARP TCDD-inducible poly(ADP-ribose) polymerase
WDR19 WD repeat domain 19